MicroRNA sequences modulating inflammation and lipid accumulation in macrophage “foam” cells: Implications for atherosclerosis

Abstract

Accumulation of macrophage “foam” cells, laden with cholesterol and cholesteryl ester, within the intima of large arteries, is a hallmark of early “fatty streak” lesions which can progress to complex, multicellular atheromatous plaques, involving lipoproteins from the bloodstream and cells of the innate and adaptive immune response. Sterol accumulation triggers induction of genes encoding proteins mediating the atheroprotective cholesterol efflux pathway. Within the arterial intima, however, this mechanism is overwhelmed, leading to distinct changes in macrophage phenotype and inflammatory status. Over the last decade marked gains have been made in understanding of the epigenetic landscape which influence macrophage function, and in particular the importance of small non-coding micro-RNA (miRNA) sequences in this context. This review identifies some of the miRNA sequences which play a key role in regulating “foam” cell formation and atherogenesis, highlighting sequences involved in cholesterol accumulation, those influencing inflammation in sterol-loaded cells, and novel sequences and pathways which may offer new strategies to influence macrophage function within atherosclerotic lesions.

Core tip: Micro-RNA (miRNA) sequences are short non-coding RNAs which play a key role in epigenetic regulation of gene transcription and translation. Significant changes in miRNA expression occur in macrophage “foam” cells, laden with cholesterol and cholesteryl ester, which contribute not only to macrophage phenotype and inflammatory status, but also to novel pathways which may influence the development of atherosclerotic lesions, the principal underlying cause of coronary heart disease. The rapid expansion of this field of research is leading to new therapeutic targets and strategies for treatment of this progressive and highly complex global disease.

INTRODUCTION

The purpose of this review is to identify and contextualise the emerging roles of micro-RNA (miRNA) sequences involved in epigenetic regulation of cholesterol deposition within macrophage “foam” cells, a rapidly developing area of key interest to researchers and clinicians developing new therapeutic strategies to combat coronary heart disease (CHD). CHD, a major cause of global morbidity and mortality, is principally caused by atherosclerosis, a complex, progressive chronic inflammatory disease. Genetic factors contribute to atherosclerosis, in combination with environmental, metabolic and behavioural triggers including elevated serum lipid levels, diabetes, obesity, hypertension and smoking[1]. Atherosclerotic lesions originate at non-random locations of the vasculature[2,3], where alterations in haemodynamic blood flow, such as decreased shear stress and turbulent flow, are sensed by endothelial cells, disrupting homeostatic cellular organisation, increasing permeability of the arteries and enabling the accumulation of circulating cholesterol-rich low-density lipoprotein (LDL) in the intima[2-4]. Local inflammation in endothelial cells is mediated by activation of the pro-inflammatory transcription factor, nuclear factor-κB (NF-κB), in part due to shear stress-mediated inhibition of the anti-inflammatory transcription factor Kruppel-like factor 2[5,6]. This leads to increased expression of adhesion molecules, E-selectin, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1, and of pro-inflammatory cytokines and chemoattractants[6]. Further, endothelial expression of lipoxygenase enzymes and production of reactive oxygen species (ROS) oxidatively modify proteoglycan-bound LDL (oxLDL)[7]. This amplifies the local inflammatory response mediated by receptors such as lectin-like oxidised LDL receptor 1 (LOX-1) and toll-like receptor 4 (TLR4) present on endothelial and smooth muscle cells[8-10].

Endothelial expression of adhesion molecules, and chemokine-chemokine receptor interactions, recruit circulating monocytes to the intima, where they differentiate into macrophages in response to macrophage colony-stimulating factor[11]. Intimal macrophages recognise modified components of oxLDL and internalise oxLDL and LDL, becoming “foam” cells due to accumulation of droplets of cholesteryl ester. This occurs via interaction with scavenger receptors (SRs), such as SR-A1, SR-B1, cluster of differentiation 36 (CD36, SR-B2), CD68 (SR-D1), LOX-1 (SR-E1), TLR4, and the LDL receptor (LDLR)[7,12-14]. Lipoprotein lipase (LPL) is also implicated in foam cell formation in distinct ways: Inhibition of LPL activity by angiopoietin-like protein 4 decreases lipid uptake in macrophages, whereas genetic deletion of this protein increases lipid uptake, expression of lipid-induced genes and respiration[15]. Additional receptor independent mechanisms such as macro- and micropinocytosis can also lead to the uptake of these lipoproteins[16,17]. The influx of cholesterol-rich lipoproteins through these various mechanisms, as well as the rate limited process of cholesterol efflux (below), leads to the generation of lipid-laden “foam” cells with reduced capacity to migrate from the intima[18-20].

Accumulation of macrophages and lipid-laden foam cells is accompanied by plaque enrichment with additional immune cells[21]. T-helper cells, activated by oxLDL-induced maturation of dendritic cells (DCs), recognise epitopes on apolipoprotein B100 (ApoB100) in native LDL and oxLDL[22,23]. Phenotypically, these T_H cells are primarily of the T_H1 subset, producing pro-inflammatory cytokines such as interferon gamma (IFN-γ) and tumour necrosis factor alpha (TNF-α), but atheroprotective anti-inflammatory regulatory T cells (T_regs) are also present[24,25]. The combination of hyperlipidaemia, endothelial expression of adhesion molecules and chemokines, and deposition of chemokines on endothelial cells by activated platelets, recruits and activates additional immune subsets, including neutrophils[26-30]. Neutrophils express myeloperoxidase that produces hypochlorous acid, that promotes LDL oxidation and foam cell formation and increases retention of LDL in the intima via binding to LPL[7,26-31].

As the complexity of the arterial microenvironment increases, atherosclerotic plaques develop a number of key features. Responding to signals such as growth factors, cytokines and oxidised phospholipids (oxPL), vascular smooth muscle cells (VSMCs) undergo phenotypic switching from contractile quiescent VSMCs to synthetic, migratory and proliferative VSMC[32,33]. This leads to dramatic vascular remodelling and arterial thickening via production of matrix degrading metalloproteinases and a shift in production from type I and III collagen to type VIII collagen[34-36]. Further, intimal VSMCs accumulate lipids and can take on a foam cell phenotype which, under endoplasmic reticulum (ER) stress or in the presence of increased intracellular free cholesterol, leads to apoptosis and necrosis of both macrophage-derived and VSMC-derived foam cells, forming a hypoxic, necrotic core and extracellular lipid pools[37-41]. Hypoxia inducible factor 1 enhances neo-vascularisation via induction of vascular endothelial growth factor A expression in macrophages and VSMC[42,43], and by increased expression of macrophage SRs and pro-inflammatory mediators and decreased expression of ATP binding cassette (ABC) transporters responsible for cellular cholesterol efflux[44-46].

Macrophage sub-populations within atherosclerotic lesions

Within the arterial intima, macrophages exhibit notable phenotypic plasticity in response to multiple signals from this complex microenvironment and can exhibit pro- or anti-atherosclerotic responses (Figure 1). Pro-inflammatory (M1) macrophages can be generated in vitro in response to a variety of stimuli associated with a T_H1 response, such as lipopolysaccharide (LPS) and IFN-γ[47,48], resulting in increased expression of pro-inflammatory mediators such as interleukin (IL)-1β, IL-6, TNF-α, IL-12 and IL-23, and ROS[47,49,50]. Oxidized LDL induces activation of the NF-κB pathway which enhances the pro-inflammatory response in M1-like macrophages and expression of pro-inflammatory mediators in macrophages polarised to the anti-inflammatory (M2) phenotype[51-53]. Further, oxLDL and individual components derived from oxLDL, such as free cholesterol and cholesterol crystals, cholesteryl ester hydroperoxides, and 7-ketocholesteryl-9-carboxynonanoate (Figure 1), have been shown to activate pro-inflammatory pathways including the nod-like receptor protein 3 (NLRP3) inflammasome[54], mitogen activated protein kinase pathway[55,56] and NF-κB signalling[57,58].

Figure 1.

Macrophage phenotype in response to lipids and other factors within atherosclerotic lesions. Oxidized low density lipoprotein particles are composed of a number of components including (modified) apolipoprotein B, (oxidized) free cholesterol, (oxidized) cholesteryl esters and (oxidized) phospholipids, which induce a range of unique transcriptional responses in macrophages (indicated by arrows), resulting in altered expression of secreted cytokines and cell surface receptors, and differing macrophage phenotypes (highlighted in bold). Macrophages can be polarised to a pro-inflammatory phenotype by components of oxidized LDL in a number of differing ways. Cholesterol crystals activate the inflammasome to increase expression of interleukin-1 (IL-1), while cholesteryl ester hydroperoxides activate phospho-extracellular signal-regulated protein kinases 1 and 2 (pERK1/2) and phospho-protein kinase B (pAkt) pathways, resulting in induction of peroxisome proliferator activated receptor alpha and increased expression of C-X-C motif ligand 8 (CXCL8) and the scavenger receptor, cluster of differentiation 36 (CD36). The modified cholesterol metabolite, 7-ketocholesterol, also triggers pAkt and pERK1/2 signalling, resulting in activation of nuclear factor kappa B (NF-κB), and enhanced output of pro-inflammatory cytokines such as IL-6 and CXCL8; this oxysterol also increases expression of CD36 and CD68, potentiating uptake of modified lipoproteins, and represses expression of ATP binding cassette transporter A1 (ABCA1) and ABCG1, limiting cholesterol removal via apolipoprotein A-I (apoA-I) and high density lipoprotein. By contrast, other components of oxLDL can induce an anti-inflammatory phenotype: For example, 9-oxononanoyl cholesterol induces expression of transforming growth factor β and stimulates fibrosis. Short chain oxidized phospholipids interact with CD36 to activate cyclooxygenase-2 (COX-2) and heme oxygenase-1 (HO-1), while long chain oxidized phospholipids bind toll-like receptor-2, resulting in activation of nuclear factor erythroid-2-related factor 2 which enhances expression of antioxidant genes, including HO-1, to protect cells against further oxidative damage. Other factors found within atherosclerotic lesions can also influence macrophage phenotype: For example, the chemokine CXCL4 induces the expression of pro-inflammatory factors such IL-6, tumor necrosis factor α, matrix metalloproteinase 7 and S100 calcium binding protein A8, while repressing the expression of ABCG1, HO-1, CD36, scavenger receptor-A and CD163. Alternatively an anti-inflammatory and antioxidant phenotype can be induced by the interaction of hemoglobin:haptoglobin complexes with CD163, which activates phospho-activating transcription factor-1, resulting in changes in LXR expression, induction of HO-1 and increased expression of IL-10 and ABCA1. IL: Interleukin; TGF: Transforming growth factor; TNF: Tumor necrosis factor; HO-1: Heme oxygenase-1; MMP: Matrix metalloproteinase; LXR: Liver X receptor; ABCA1: ATP binding cassette transporter A1; HDL: High density lipoprotein; pAkt: Phospho-protein kinase B; NF-κB: Nuclear factor kappa B; pATF-1: Phospho-activating transcription factor-1; PPAR-α: Peroxisome proliferator activated receptor alpha; CXCL: C-X-C motif ligand; ABCG1: ATP binding cassette transporter G1.

Macrophages, however, can adopt a variety of additional immunoregulatory subtypes within the phenotypic spectrum. A subset of anti-inflammatory macrophages (M2a), generated in response to cytokines such as IL-4 and IL-13, are produced as part of the T_H2 response[59,60]. These cells are associated with wound healing via production of factors such as fibronectin and transforming growth factor β (TGF-β)[59,60]. Exposure to immune complexes, and to TLR ligands, generates another subset, termed M2b, which have both protective and detrimental roles and express high levels of the anti-inflammatory cytokine IL-10, low levels of pro-inflammatory IL-12, but also other pro-inflammatory mediators including chemoattractant C-C motif chemokine ligand 1 (CCL1)[61-63]. Stimulation of macrophages with glucocorticoids and IL-10 induce macrophage phenotype (M2c), which play a predominant role in clearance of apoptotic cells[64,65]. Finally, a pro-angiogenic population, termed M2d, is induced in murine macrophages in response to adenosine agonists in conjunction with TLR-signalling[66,67].

Interestingly, while some components of oxLDL activate inflammatory pathways, oxysterols and the product of cholesteryl ester oxidation, 9-oxonanoyl cholesterol, induce expression of the anti-inflammatory and pro-fibrotic cytokine TGF-β[68,69]. Consequently, treatment of macrophages with oxLDL can also induce an anti-inflammatory phenotype[70]. This apparent discrepancy between inflammatory versus anti-inflammatory signalling may be due to the degree of oxidation of the LDL particle[71], or the extent of lipid accumulation within cells[72]. Oxidized phospholipids (oxPL) (Figure 1) also induce a distinct macrophage phenotype (Mox) in murine models[73-75]; Mox macrophages exhibit reduced expression of M1, as well as M2-like, macrophage markers and enhanced expression of nuclear factor erythroid 2-related factor 2 (Nrf2) dependent anti-oxidant genes[73]. Further, macrophage subsets found within the plaque microenvironment include M4 macrophages, which are induced by chemokine (C-X-C) motif ligand 4 (CXCL4)[76], MHb macrophages, induced by hemoglobin: Haptoglobin complexes[77], and Mhem macrophages, induced by heme[78,79]; both MHb and Mhem macrophages exhibit resistance to cholesterol loading[77-79].

Cholesterol accumulation in macrophage “foam” cells: Responses to excess (oxy)sterol

Macrophages play a vital role in handling excess LDL-cholesterol and/or toxic oxLDL metabolites, via esterification to cytosolic lipid droplets by Acyl CoA: Cholesterol Acyltransferase (ACAT-1-/2) or lysosomal sequestration[80]. Autophagy also contributes to lipid droplet formation, with Beclin-1 inhibiting the formation of droplets in response to modified LDL in naïve cells but not in inflammatory activated macrophages[81]. Accumulation of sterol is central to activation of nuclear liver X receptors (LXRs), which lie under the control of oxysterol metabolites of cholesterol; the extent of activation of these transcription factors may also contribute to the heterogeneity of macrophage responses to sterol accumulation[72,82]. LXRs control the expression of ABC transporters (ABCA1, ABCG1/G4) that actively efflux cholesterol from cells to acceptors, such as apolipoprotein (apo) A-I, apoE and high-density lipoprotein (HDL). Binding of apoA-I to ABCA1 triggers an array of cell signalling pathways[83], and mobilisation of stored cholesteryl esters via cholesteryl ester hydrolases, releases cholesterol which trafficks to the plasma membrane for efflux as nascent HDL[80,84]. In addition, ABCG1 and ABCG4 aid the formation of more mature forms of HDL, so they work in concert with ABCA1 to initiate the process of reverse cholesterol transport which can return cholesterol to the liver for excretion via the classical and alternative bile acid pathways[80,84].

Liver X nuclear receptors form obligate heterodimers with retinoid X receptors which bind directly to the LXR response element, a direct repeat 4 (DR4) motif of the six base pair sequence AGTTCA separated by four base pairs[85-88]. Ligand binding triggers a conformational change in the heterodimer, dissociating nuclear receptor co-repressors [NCOR1/NCOR2 (SMRT)] proteins which undergo ubiquitination and proteasomal degradation, and engaging coactivator proteins (steroid receptor coactivators, PPAR-γ coactivator 1 and nuclear receptor coactivator 6)[87]. Genetic deletion of LXRs in bone marrow derived macrophages, however, reveal a more complex picture: Depending on the target gene, LXR deletion can up- or down-regulate, or effect no change in, gene expression[87].

LXRs contribute to the inactivation of the counter-regulatory system operated by sterol regulatory binding proteins (SREBPs) which belong to the basic helix-loop-helix leucine zipper (bHLH-Zip) family of transcription factors[89]. Three SREBP isoforms exist, encoded by two genes: SREBF1 (SREBP-1a and SREBP-1c) and SREBF2 (SREBP-2) which target sterol response elements (SRE). Unlike SREBP-1a which is constitutively expressed and targets all SRE with low specificity, SREBP-1c and SREBP-2 are inducible and regulate the expression of genes encoding proteins involved in fatty acid and cholesterol metabolism, respectively[89,90]; SREBP-2 also transcriptionally regulates the LDL receptor which mediates endocytosis of LDL from the circulation. In sterol-replete cells, SREBP transcription factors remain inactive, sequestered at the ER by binding to a chaperone, SREBP cleavage activating protein (SCAP), which contains a five transmembrane sterol sensing domain and interacts with the ER anchor, insulin-induced gene (INSIG-1/-2). As cholesterol levels fall, the interaction of SCAP with INSIG is lost, allowing SCAP-SREBP to traffick to the Golgi apparatus via inclusion in COPII-vesicles[89,90]. Golgi site-1 and site-2 proteases (SP-1, SP-2) cleave the amino terminal of SREBP-2, releasing a transcriptionally active fragment which is imported into the nucleus to target sterol-responsive genes, including SREBF2 itself; rapid degradation of nuclear (nSREBP) serves to terminate this signalling pathway[89,90].

LXRs operate in functional opposition to SREBP-2, repressing cholesterol biosynthesis via novel negative LXR DNA-response elements in the promoter region of genes encoding squalene synthase and lanosterol 14-demethylase[91-93], and promoting the degradation of LDL receptors by increasing the expression of proprotein convertase subtilisin/kexin type 9 (PCSK9)[94,95]. The E3 ubiquitin ligase, inducible degrader of the LDL receptor (IDOL) is an LXR target gene: IDOL dimers interact with members of the ubiquitin-conjugating enzyme (UBE) 2D family of E2 ubiquitin ligases to transfer ubiquitin to the cytoplasmic tail of members of the LDL receptor family, promoting receptor degradation[94,95]. Oxysterols also bind to Insig-1/2, sequestering SREBPs at the ER, further ensuring repression of cholesterol biosynthesis and uptake[88]. By contrast, LXR agonists induce gene expression of SREBP-1c; fatty acid synthase, and a number of desaturase and elongase enzymes in the fatty acid biosynthetic pathway, are also directly regulated by LXR[87]. Thus, efficient delivery of cholesterol to the ER is needed to inhibit proteolytic processing of SREBP-1c to an active transcription factor[89,90], and to limit increased biosynthesis of fatty acids[87].

LXRs also exert anti-inflammatory effects, some of which are indirect and due to the increased expression of ABCA1[96], and production of anti-inflammatory HDL[97,98]. HDL inhibit TLR signalling in macrophages and cytokine signalling in bone marrow progenitors by removal of cholesterol from lipid rafts[99,100] and induce activating transcription factor 3, suppressing the expression of pro-inflammatory genes[97,98]. Multiple mechanisms exist by which LXRs modulate inflammatory responses, some of which involve transactivation and others transrepression[86-88]. Pathway-specific responses occur: LXR activation inhibits NF-κB dependent induction of pro-inflammatory genes in response to LPS and responses triggered by TLR4 and TNF-α but exerts minimal impact on the pathway mediated by TLR3[86-88]. LXRs also regulate apoptosis and enhance survival of macrophages within lesions, while IFN-γ promotes neointimal hyperplasia and macrophage apoptosis by promoting ubiquitin-dependent LXR degradation[101,102].

However, it should be recognised that the pharmacology of oxysterols is highly complex: A large number of nuclear, and G-protein coupled (GPR), receptors bind these bioactive lipids [e.g., retinoid-related orphan receptors, ER, Epstein-Barr virus induced GPR (EBI2/GPR183) and IL-8 receptor (CXCR2)][93]. This, combined with the complexity of oxysterol metabolism, enzymatic conversion to other species such as esters, bile acids and 3-sulphate derivatives, and tissue- and species-specific effects, makes deciphering the (patho)physiological impact of these molecules particularly challenging[93].

EPIGENETIC MECHANISMS CONTRIBUTING TO “foam cell” FORMATION: THE EMERGING ROLE OF MICRORNA

It is increasingly clear that epigenetic mechanisms such as DNA methylation, histone post-translational modification and changes in expression of non-coding RNA, such as long non-coding RNA (lncRNA) and miRNA, are important contributors to macrophage phenotype and the pathogenesis of “foam cell” formation. Alterations in chromatin structure and gene expression exert both acute and chronic effects on a wide array of biological processes which influence macrophage lipid accumulation and inflammatory responses. For example, DNA methyltransferases catalyse methylation of the 5’-position of cytosine residues, using S-adenosyl-methionine as the methyl donor, resulting in hypermethylation of CpG islands and stable repression of transcription[103,104]. Chromatin histone post-translational modifiers, such as histone acetyltransferases and deacetylases and histone methyltransferases, target lysine and/or arginine residues to induce or repress gene expression, dynamically fine-tuning gene expression by controlling the access of transcription factors to promoter and enhancer regions[105,106].

An additional layer of epigenetic regulation is provided by non-coding RNA sequences, including lncRNA sequences, longer than 200 nucleotides, and miRNA sequences (20-25 nucleotides in size), the focus of this review article, which fine-tune expression of multiple (networks of) genes in response to environmental factors, including oxLDL[107-109]. Sequences encoding miRNA can be found singly or in clusters throughout the genome, located in intron-exon portions of protein-encoding genes or intergenic regions[110,111]. Transcription is dependent on the activity of RNA polymerase II/III and expression, in relation to intergenic miRNA, can be dependent or independent of host gene expression[111-114]. MicroRNA are frequently found in clusters and can be co-transcribed and separated by splicing, or expressed independently[115]. Transcription and generation of miRNA occurs through both canonical and non-canonical pathways, with less information available on the latter[116]. The canonical pathway involves generation of a hairpin-containing primary miRNA (pri-miRNA) transcript containing a 5’ methylated cap and a 3’ polyadenylated tail required for pri-miRNA processing and transport[112,117]. Processing occurs via a microprocessor complex consisting of the double-stranded RNA-binding protein DiGeorge syndrome critical region gene 8 which recognises methyl motifs present in the pri-miRNA[118,119]. This interaction serves as an anchor for a ribonuclease II (RNase III), known as Drosha, which cleaves the hairpin structure from the pri-miRNA transcript generating precursor miRNA (pre-miRNA)[120-122].

Export of pre-miRNA (around 70 nucleotides in length) from the nucleus involves the nucleocytoplasmic transporter factor exportin-5 and Ras-related nuclear protein (Ran)GTP[123]. Recognition and binding to exportin-5 occurs primarily through interaction with the 3’ overhanging sequence of pre-miRNA. Blunt ended pre-miRNA remain capable of interaction while RanGTP is bound to the hairpin structure, following release into the cytoplasm[124,125]; hydrolysis of GTP to GDP results in release of the pre-miRNA[118]. Once localised in the cytoplasm, pre-miRNA is processed by a second RNase III enzyme, Dicer, to a mature miRNA duplex (19-25 nucleotides) through removal of the stem-loop structure[126,127]. The guide strand, which has lower base pairing stability, is loaded onto the RNA-induced silencing complex (RISC) composed of Dicer, transactivation response (TAR) RNA binding protein (TRBP) and Argonaute proteins (1 to 4). After integration into the active RISC complex, miRNAs base pair with their complementary mRNA molecules, guided by their miRNA recognising element[128,129].

Degradation of target mRNA occurs only when the miRNA and the target mRNA match exactly (perfect match) or are nearly exactly complementary to each other; this process is the same as the RNA interference induced by artificial small interfering RNA (siRNA)[130,131]. By contrast, if the complementarity between miRNA and target mRNA is only partial (imperfect match), then more moderate reductions in mRNA levels accompanied by translational repression will occur. Targeting occurs through binding of the seed sequence of RISC-incorporated miRNA to conserved complementary regions found in the 3’UTR of target mRNA[130,131]. Factors such as AU-rich regions near seed region binding sites, and auxiliary binding of the miRNA to transcript can also play a role in determining target specificity, reducing translational efficiency or inducing mRNA destabilisation via deadenylation[132-134]. miRNA also exert regulatory functions on gene expression in the nucleus, paradoxically promoting gene expression in certain conditions[135,136]. In eukaryotic cells, miRNA molecules can bind several target sequences, mainly within the 3’-UTR of mRNA with varying degrees of complementarity, so that each single miRNA is able to interact with and regulate a large number of genes. Computational prediction suggests that more than 60% of all mammalian protein-coding genes are conserved targets of miRNA, while each miRNA has target sites in hundreds of different genes[137,138]; miRNAs also display tissue-specific expression[139] and concentration-dependent effects in pathologically affected organs and tissues[140-142].

miRNA not only regulate the transcriptional landscape of the cell, but some sequences exist in the extracellular environment in a variety of different forms; degradation of miRNA is avoided through association with Argonaute RISC catalytic component 2 (Ago2), and to a lesser extent nucleophosmin 1 (NMP1)[143-145]. miRNA are found enriched in extracellular vesicles such as exosomes, microvesicles, and lipoproteins such as HDL[146-148], and represent novel biomarkers of atherosclerosis[149]. Secreted miRNA may elicit pro- and anti-atherosclerotic functions: EC when placed under conditions of atherogenic shear stress release Ago2-bound miR-126-3p which in turn downregulate contractile VSMC markers[150], while delivery of miR-223 by HDL to EC leads to downregulation of ICAM-1[151,152].

miRNA sequences implicated in macrophage “foam” cell formation

Over the last five years, there has been an explosion of interest in the role of miRNA involved in macrophage biology, and in “foam” cell formation in particular. Table 1[153,155-204] indicates some of the miRNA sequences identified by interrogation of the NCBI PubMed database, as either altered by uptake of modified LDL by macrophages, or implicated in the pathogenesis of foam cell formation. Many of the genes targeted by these sequences play established roles in either lipid metabolism or inflammation, but a significant number have no prior links to either process, highlighting the importance of miRNA research in driving the discovery of novel cellular processes contributing to disease.

Table 1.

MicroRNA sequences associated with macrophage ”foam cell” formation and atheroma

MicroRNA (↑↓)	Macrophage	Stimulus	Target	Outcomes in vitro	Outcomes in vivo	Ref.
Lethal: (let)-7g-5p (↓)	Human: THP-1 macrophages	Oxidized low density lipoprotein (oxLDL)	Nuclear factor kappa beta (NF-κB) (canonical and non-canonical pathways)	Inhibits phosphorylation of inhibitor kappa B kinase (IKK-κB and inhibitor (I) κB, downregulates sterol regulatory element binding transcription factor (SREBF2) and upregulates ATP binding cassette (ABC) transporter A1 (ABCA1); reduces expression of mitogen-activated protein kinase kinase kinase 1 (MEKK1), IKK-κ and inhibits IKK-κ phosphorylation	Overexpression of let-7 g in apolipoprotein (apo)E-/- mice fed a high fat diet (HFD) reduces macrophage accumulation and aortic plaque area; let-7 g sponge accelerates aortic macrophage accumulation in the same model	Wang et al[155], 2017
miR-7-5p	Human: THP-1 macrophages	oxLDL ± puerarin	Serine/threonine kinase 11 (STK11)	Mimic significantly decreases cholesterol efflux and promotes cholesterol deposition	-	Li et al[156], 2017
miR-9-5p	Human: THP-1 macrophages	oxLDL	Acyl CoA: Cholesterol acyltransferase (ACAT-1; SOAT1)	Mimic decreases levels of ACAT-1 protein, reduces cholesterol esterification and blocks foam cell formation	-	Xu et al[157], 2013
miR-10a-5p	Murine: ApoE-/- macrophages	Deletion of dicer	-	Mimic rescues defective oxidation of fatty acids in alternatively activated Dicer-deficient macrophages, limiting foam cell formation and inflammation	Levels of hsa-miR-10a are negatively linked to atheroma progression; blockade of miR-10a exacerbates atheroma in apoE-/- mice (HFD)	Wei et al[158], 2018
miR-16-5p (↓)	Murine: RAW 264.7 macrophages	OxLDL	Programmed cell death 4 (PDCD4)	Mimic decreases expression and secretion of pro-inflammatory cytokines (interleukin (IL)-6, Tumour necrosis factor (TNF-α), promotes that of anti-inflammatory IL-10, and suppresses NF-κB expression; inhibitor achieves the reverse	Levels decreased in atheroma in apoE-/- (HFD)	Liang et al[159], 2016
miR-17-5p	Human: THP-1 macrophages	oxLDL	Beclin-1	Mimic inhibits the enhancement of autophagy and cholesterol efflux induced by interferon-stimulated gene 15 (ISG15)	-	Huang et al[160], 2018
miR-19a-3p	-	-	HMG-Box transcription factor-1 (HBP-1)	-	Serum levels are elevated in atherosclerotic patients, and in aortae susceptible to atherosclerosis. Inhibition decreases atheroma and aortic lipid accumulation in apoE-/- (HFD) mice	Chen et al[161], 2017
miR-19b-3p (↑)	Human: THP-1 macrophages; Murine: Peritoneal macrophages	Acetylated LDL (AcLDL)	ABCA1	Mimic inhibits cholesterol efflux to ApoA-I, increasing cholesterol mass	Overexpression of miR-19b decreases reverse cholesterol transport (RCT) in vivo; mimic reduces high density lipoprotein (HDL) levels, increases lesion area and lipid content in apoE-/- mice fed a Western diet (WD); inhibitor achieves the reverse	Lv et al[162], 2014
miR-19b-3p (↓)	Human: THP-1 macrophages; Murine: Peritoneal macrophages	AcLDL + diosgenin	ABCA1	Inhibitor enhances ABCA1 cholesterol efflux	Inhibitor promotes RCT in vivo, elevates HDL levels, reduces aortic lipid deposition and plaque area in apoE-/- mice (WD)	Lv et al[163], 2015
miR-20a/b (-5p)	Human: THP-1 macrophages; Murine: RAW264.7 macrophages	oxLDL	ABCA1	Mimic decreases cholesterol efflux to apoA-I, and increases macrophage cholesterol content	Mimic reduces hepatic expression of ABCA1 and high-density lipoprotein (HDL) levels, impairs reverse cholesterol transport and promotes atherogenesis in apoE-/- mice	Liang et al[164], 2017
miR-21-5p	Murine: RAW 264.7 macrophages	OxLDL ± LPS (lipopoly-saccharide)	Toll like receptor 4 (TLR4); NF-κB	LPS stimulation of miR-21 inhibits foam cell formation and reduces secretion of IL-6, IL-12, TNF-α	-	Feng et al[165], 2014
miR-21-5p	Murine: Bone-marrow derived macrophages	AcLDL	Mitogen-activated protein kinase kinase 3 (MKK3)	MiR21-/- macrophages exhibit increased ABCG1 degradation and decreased cholesterol efflux, enhancing foam cell formation.	Most abundant miR in murine macrophages; levels elevated in aortic plaque macrophages isolated from LDL receptor knockout (Ldlr-/-) (WD) mice; knockout of miR-21 enhances arterial macrophage accumulation, production of inflammatory cytokines	Canfrán-Duque et al[166], 2017
miR-23a-5p (↑) miR-23a-3p	Murine: RAW 264.7 macrophages	oxLDL	ABCA1/G1	Inhibitor enhances cholesterol efflux and decreases foam cell formation via upregulation of ABCA1/G1 expression	Plasma levels correlate with plaque progression and vulnerability in patient with acute ischemic stroke. Long-term systemic delivery of antagomir reduces atheroma and promotes plaque stability (apoE-/- mice)	Yang et al[167], 2018
miR-24-3p	Primary: Human monocyte-derived macrophages	Colony stimulating factor (CSF)	Matrix metallo-proteinase (MMP)-14	Inhibitor increases macrophage invasive capacity	Hsa-miR-24 levels inversely correlate with MMP-14 protein, and lesion instability Inhibitor increases lesion size and MMP-14 levels in apoE-/- mice (HFD)	Di Gregoli et al[168], 2014
miR-27a/b (-3p)	Human: THP-1 macrophages; Murine: RAW264.7 macrophages	AcLDL	ABCA1	Mimic decreases cholesterol efflux, and increases free cholesterol content in macrophages, but blocks uptake of oxLDL [Lipoprotein lipase (LPL), cluster of differentiation (CD36)] and inhibits cholesterol esterification	-	Zhang et al[169], 2014
miR-28a-5p (↑)	Murine: RAW264.7 macrophages	oxLDL	LDL receptor class A domain containing 3 (LRAD3)	-	-	Li et al[170], 2018
miR-30c-5p	Human: THP-1 macrophages	oxLDL	Caspase 3	Cluster differentiation (CD) 36-dependent uptake of oxLDL reduces miR-30c-5p, enhancing IL secretion	Low serum levels of hsa-miR-30c-5p predict carotid atherosclerosis. Antagomir impairs endothelial healing following carotid injury (C57BL/6J mice)	Ceolotto et al[171], 2017
miR-30c-1-3p (↑)	Murine: RAW264.7 macrophages	oxLDL	Oxidized LDL (lectin-like) receptor 1 (LOX-1)	-	-	Li et al[170], 2018
miR-33a/b (-5p) (↑)	Human: THP-1 macrophages	oxLDL ± C. pneumoniae	ABCA1	Inhibitor promotes cholesterol efflux compared with C. pneumoniae control	-	Zhao et al[172], 2014
miR-33a-5p	Human: THP-1 macrophages	Vaspin ± LPS	ABCA1	Vaspin decreases expression of miR-33a via inhibition of NF-κB, enhancing cholesterol efflux	-	Gao et al[173], 2018
miR-33	Human: THP-1 macrophages; Murine: Peritoneal macrophages	-	Peroxisome proliferator activator receptor coactivator 1 (PGC1A), pyruvate dehydrogenase kinase 4 (PDK4), solute carrier family 25 member 25 (SLC25A25), nuclear respiratory factor 1 (NRF1), transcription factor A, mitochondrial (TFAM)	Inhibitor enhances mitochondrial respiration, and cholesterol efflux to apoA-I	Antagomir reduces atheroma in apoE-/- mice (WD)	Karunakaran et al[154], 2015
miR-33	Murine: Peritoneal macrophages	AcLDL	Autophagy protein 5 (Atg5); autophagy-related 12 (Atg12), microtubule-associated protein light chain 3 (Map11c3b), AMP-activated protein kinase κ1 (Prkaa1), lysosomal associated membrane protein 1 (Lamp1), transcription factor EB (TFEB), Forkhead box O-3 (FOXO3)	Mimic inhibits the breakdown of lipid droplets by repressing effectors of macrophage autophagy. Silencing promotes lipid droplet catabolism, aiding ABCA1-dependent cholesterol efflux	Inhibition restores defective autophagy in aorta and macrophages of Ldlr-/- mice	Ouimet et al[153], 2017
miR-33a-5p (↑)	Human: THP-1 macrophages	oxLDL	ABCA1	Mimic decreases the expression of ABCA1 and promotes lipid accumulation in macrophages, while the inhibitor achieves the reverse	Levels are elevated in individuals at risk of atherosclerosis	Kim et al[174], 2017
miR-34a-5p (↓)	Human: THP-1 macrophages	oxLDL + Hcy	Histone deacetylase 1 (HDAC1)	Overexpression of miR-34a reduces HDAC1 levels in foam cells, while knockdown achieves the reverse; HDAC1 induces homocysteine (Hcy) dependent foam cell formation	Levels of miR-34a decrease, and expression of HDAC1 increases, in the aorta of apoE-/- mice fed a high methionine diet	Zhao et al[175], 2017
miR-98-5p (↓)	Murine: Peritoneal macrophages	oxLDL	Oxidized LDL (lectin-like) receptor 1 (LOX-1)	Mimic reduces expression of LOX-1 and inhibits foam cell formation; inhibitor achieves the reverse	Mimic decreases expression of LOX-1 and lipid accumulation in the aortic root in apoE-/- mice (HFD); inhibitor achieves the reverse	Dai et al[176], 2018
miR-125b-5p (↑)	Murine: RAW 264.7 macrophages	LPS	NF-κB	Silencing of CD40 downregulates levels of miR-125; LPS stimulates miR-125b expression	miR-125b levels are increased in atherosclerosis; siRNA-CD40 apoE-/- mice exhibit reductions in lesion area	Hueso et al[177], 2016
miR-128- (↓)	Murine: RAW 264.7 macrophages	oxLDL	-	Mimic reverses the pro-atherogenic impact of long non-coding (lnc)RNA NEAT1 on foam cell formation	-	Chen et al[178], 2018
miR-133a	Murine: RAW 264.7 macrophages	oxLDL	Testicular orphan nuclear receptor 4 (TR4)	Mimic prevents TR-4 mediated enhancement of lipid uptake via CD36	-	Peng et al[179], 2016
miR-134-5p	Human: THP-1 macrophages	oxLDL	Angiopoietin (ANGTPL)/lipoprotein lipase (LPL)	LPL activity and protein, inflammatory cytokines and cholesterol mass enhanced by miR-134 mimic; inverse achieved using an inhibitor	-	Lan et al[180], 2016
miR-134-5p	-	-	ANGTPL4/LPL	-	Mimic increases atherosclerotic lesions, release of proinflammatory cytokines and peritoneal macrophage lipid accumulation in apoE-/-(HFD) mice; inhibitor achieves the reverse	Ye et al[181], 2018
miR-144-3p	Human: THP-1 macrophages;Murine: Peritoneal and J774.1 macrophages	Liver X receptor ligand T0901317	ABCA1	Mimic reduces cholesterol efflux to apoA-I in macrophages	Mimic reduces HDL levels in vivo (C57BL/6); inhibitor achieves the reverse	Ramirez et al[182], 2013
miR-144-3p	Human: THP-1 macrophages	oxLDL	ABCA1	Mimic reduces cholesterol efflux and enhances expression of cytokines (IL-1, TNF-α, IL-6)	Agomir inhibits RCT in vivo, and accelerates atherosclerosis in apoE-/- mice (HFD). Circulating levels of miR-144-3p correlate with acute myocardial infarction	Hu et al[183], 2014
miR-146a-5p	Murine: Peritoneal macrophages (wild type and apoE-/-)		NF-κB	Increases in miR-146a inhibit pro-inflammatory responses in macrophages (TNF-α)	miR-146a mimic inhibits inflammation and plaque development in apoE-/- x Ldlr-/- and Ldlr-/- mice (HFD)	Li et al[184], 2015
miR-146b-5p (↑)	Human: THP-1 macrophages	oxLDL	TNF receptor (TNFR) associated factor 6 (TRAF6)	Inhibition promotes inflammation and lipid uptake during formation of foam cells	Levels are elevated in foam cells, and clinical specimens from patients with atherosclerosis	Lin et al[185], 2017
miR-148a-5p miR-152-3p	-	-	DNA methyl-transferase 1 (DNMT1)	Viral overexpression reduces expression of DNMT1, increases levels of adipocyte differentiation related protein (ADRP) and enhances cholesterol accumulation in foam cells; down-regulation achieves the reverse	Aortic levels increased in hyperhomo-cysteinaemic apoE-/- mice	Yang et al[186], 2017
miR-150-5p (↑)	Human: THP-1 macrophages	oxLDL	Adiponectin receptor 2 (ADIPOR2)	Mimic inhibits lipid accumulation, increasing cholesterol efflux to apoA-I and HDL; an inhibitor achieves the reverse. Down-regulation of ADIPOR2 replicates the impact of the miR-150 mimic	-	Li et al[187], 2016
miR-155-5p (↑)	Human: Peripheral blood monocytes	oxLDL	-	-	-	Chen et al[178], 2009
miR-155-5p (↑)	Murine: RAW 264.7 macrophages	oxLDL	HMG-box transcription factor 1 (HBP1)	Enhances lipid uptake and reactive oxygen species production by macrophages	Antagomir decreases lipid accumulation in macrophages and lesion formation in apoE-/- mice (HFD). Level is up-regulated in CD14+ monocytes from coronary heart disease (CHD) patients	Tian et al[188], 2014
miR-155-5p (↑)	Human: THP-1 macrophages	oxLDL	Calcium-regulated heat stable protein 1 (CARHPS1)-TNF-α	Mimic blocks lipid uptake and suppresses expression of TNF-α; inhibitor achieves the reverse	Elevated in clinical samples (plaque and plasma) from patients with atherosclerosis	Li et al[189], 2016
miR-155-5p	Human: THP-1 macrophages	-	T-cell immunoglobulin and mucin domain-3 (Tim-3)	Mimic enhances expression of cholesteryl ester (CE) hydrolase (CEH). Overexpression inhibits foam cell formation, intracellular CE accumulation and enhances efflux of cholesterol	-	Zhang et al[190], 2018
miR-181a-5p (↓)	Human: THP-1 macrophages	oxLDL	Mitogen-activated protein kinase kinase 1 (MEK1)	Activates MEK/ERK/NF-κB, upregulates NLR family leucine-rich repeat protein 3 (NRLP3) inflammasome-related proteins (NRLP, caspase-1, IL-18, IL-1)	-	Song et al[191], 2019
miR-181a-5p (↑)	Human: THP-1 macrophages	oxLDL	Toll-like receptor 4 (TLR4)	Decreases expression of CD36 protein, and lipid [Total cholesterol (TC), Triglyceride (TG)] accumulation. Inhibits THP-1 apoptosis, and increases Il-6, IL-1, TNF-α protein expression	-	Du et al[192], 2018
miR-188-3p (↑)	-	-	-	-	Overexpression induces intravascular lipid accumulation, suppresses oxidation and macrophage inflammation in apoE-/- mice, and reduces serum levels of Regulated upon activation normal T-cell expressed and secreted (RANTES), LOX1 and inducible Nitric Oxide Synthase (iNOS)	Zhang et al[193], 2018
miR-212-3p	Human: THP-1 macrophages	oxLDL	Sirtuin 1 (SIRT1)	Overexpression promotes lipid accumulation during foam cell formation, and reduces ABCA1 expression and cholesterol efflux; depletion achieves the reverse	Levels are decreased in atheroma and macrophages in apoE-/- mice (HFD)	Miao et al[194], 2018
miR-216a-5p	Human: THP-1 macrophages	oxLDL	Cystathionine-γ-lyase (CSE)	Mimic inhibits expression of ABCA1, decreases phosphorylation of phosphatidyl-inositol 3-kinase (PI3K) and protein kinase B (AKT), and reduces ABCA1 expression and cholesterol efflux, promoting lipid accumulation; inverse occurs with the inhibitor	-	Gong et al[195], 2016
miR-217	-	-	-	-	Serum levels are negatively correlated with plaque development in apoE-/- mice (HFD). Mimic reduces intimal media thickness, reduces levels of pro-atherogenic lipoproteins and inhibits inflammation in the same model	Liu et al[196], 2018
miR-221-3p (↓)	Murine: RAW 264.7 macrophages	oxLDL	A disintegrin and metalloprotease-22 (ADAM22)	Mimic reduces foam cell formation and apoptosis; inhibitor achieves the reverse	-	Zhuang et al[197], 2019
miR-223 (↓)	Murine: Bone marrow derived macrophages; Murine: RAW264.7 macrophages	LPS, oxLDL	TLR4	Overexpression reduces foam cell formation, and production of pro-inflammatory cytokines via repression of NK-κB signaling; inhibitor achieves the reverse	Elevated levels in aortic lesions in apoE-/- mice (HFD)	Wang et al[198], 2015
mir-302a-3p (↓)	Primary: Mouse macrophages	oxLDL, AcLDL	ABCA1	Mimic decreases cholesterol efflux to apoA-I	Inhibitor enhances ABCA1 in hepatic and aortic tissues of Ldlr-/- mice (HFD), increases HDL and reduces plaque size and inflammation	Meiler et al[199], 2015
miR-361-5p	Human: THP-1 macrophages	oxLDL	LPL	Mir-361-5p is upregulated by apelin, resulting in suppression of LPL translation, inhibition of lipid accumulation and proinflammatory cytokine secretion	-	Zhang et al[200], 2017
miR-378-3p (↑)	Human: THP-1 macrophages; Murine: J774.1 macrophages	oxLDL ± coenzyme Q10	ABCG1	Coenzyme Q10 (Q10) protects cholesterol efflux by reducing expression of miR-378	Q10 promotes RCT and reduces atheroma in apoE-/- mice (HFD)	Wang et al[201], 2014
miR-382-5p (↑)	Human: THP-1 macrophages	oxLDL, AcLDL	Nuclear factor 1A (NFIA)	Mimic increases cholesterol content and reduces cholesterol efflux; enhances LPS-stimulated production of pro-inflammatory cytokines (IL-6, TNF-α, IL-1)	-	Hu et al[108], 2015
miR-486-5p	Human: THP-1 macrophages	oxLDL	Histone acetyl-transferase 1 (HAT1)	Mimic downregulates the expression of ABCA1, limiting cholesterol efflux and promoting foam cell formation; inhibitor achieves the reverse	-	Liu et al[202], 2016
miR-497-5p (↑)	Human: THP-1 macrophages	oxLDL	Apelin	Overexpression of miR-497 promotes cholesterol efflux and decreases cholesterol efflux; inhibitor achieves the reverse	-	Cui et al[203], 2017
miR-758-5p	Human: THP-1 macrophages	oxLDL	CD36	Mimic decreases uptake of DiI-labelled OxLDL via modulation of CD36; inhibitor achieves the reverse	-	Li et al[204], 2017

TargetScan and miRDB were used to confirm mouse miRNA target prediction in humans; where (↑↓) is not indicated, the level of miRNA was not confirmed altered by macrophage lipid accumulation. ABCA1: ATP binding cassette transporter A1; ABCG1: ATP binding cassette transporter G1; oxLDL: Oxidized low density lipoprotein; AcLDL: Acetylated low density lipoprotein; ADAM22: A disintegrin and metalloprotease-22; ADIPOR2: Adiponectin receptor 2); ADRP: Adipocyte differentiation related protein; AKT: Protein kinase B; ANGTPTL4: Angiopoetin-like 4; ApoE: Apolipoprotein E; ATG5: Autophagy protein 5; ATG12: Autophagy-related 12; CARHPS1: Calcium-regulated heat stable protein 1; CD: Cluster of differentiation; CEH: Cholesteryl ester hydrolase 1; CSE: Cystathionine-γ-lyase; CSF: Colony stimulating factors; DNMT1: DNA methyltransferase 1; ERK: extracellular signal-regulated kinase; FOXO3: Forkhead protein O3; HAT1: Histone acetyltransferase 1; HBP-1: HMG-Box transcription factor 1; Hcy: Homocysteine; HDAC1: Histone deacetylase 1; HFD: High fat diet; IL: Interleukin; ISG15: Interferon-stimulated gene 15; IKKα/β: Inhibitor kappa B kinase alpha/beta; iNOS: Inducible nitric oxide synthase; Lamp1: Lysosomal associated membrane protein 1; lncRNA: Long noncoding RNA; LPL: Lipoprotein lipase; LPS: Lipopolysaccharide; LRAD3: Low density lipoprotein receptor class A domain containing 3; Map11c3b: LC3 microtubule-associated protein light chain 3; MEK1: Mitogen activated protein kinase kinase 1; MEKK1: Mitogen-activated protein kinase kinase kinase 1; MKK3: Mitogen activated protein kinase kinase 3; MMP-14: Matrix metalloproteinase-14; NF-κB: Nuclear factor kappa B; NFAM: Transcription factor A, mitochondrial; NFIA: Nuclear factor 1A; NLRP3: NLR-family, leucine-rich repeat protein 3; NRF1: Nuclear respiratory factor 1; OLR1/LOX1: Oxidized low density lipoprotein (lectin-like) receptor 1; PDCD4: Programmed cell death 4; PDK4: Pyruvate dehydrogenase kinase 4; PGC1-γ: Peroxisome proliferator activated receptor-γ coactivator 1; PI3K: Phosphatidylinositol 3-kinase; Prkaa1: AMP-activated protein kinase-α1; RANTES: Regulated upon activation normal T cell expressed and secreted; SIRT1: Sirtuin 1, NAD-dependent protein deacetylase sirtuin 1; SLC25A25: Solute carrier family 25, member 25; SREBF: Sterol regulatory element-binding transcription factor; STK11: Serine/threonine kinase 11; TC: Total cholesterol; TFEB: Transcription factor EB; TG: Triglyceride; TLR4: Toll-like receptor 4; Tim-3: T-cell immunoglobulin and mucin domain-3; TNF-α: Tumour necrosis factor alpha; TR4: Testicular orphan nuclear receptor 4; TRAF6: TNF receptor (TNFR) associated factor 6; Vaspin: Visceral adipose tissue-derived serine protease inhibitor; WD: Western diet.

Multiple miRNA sequences target genes involved in macrophage cholesterol homeostasis

It is well established that miR-33, encoded by an intronic sequence within SREBF2, plays a role in modulating cholesterol metabolism, in part by repressing expression of ABCA1[152]. However, this sequence also represses effectors of macrophage autophagy[153] thereby inhibiting the breakdown of lipid droplets, and targets genes central to mitochondrial respiration, which are needed for effective cholesterol efflux to apoA-I[154]. The expressions of ABCA1 and/or ABCG1 within the cholesterol efflux pathway are also targeted by miR-19b[162], miR-20a/b[164], miR-23a-5p[167], miR-27a/b[169], miR-144[182] and miR-378[201] (Table 1), highlighting the complexity of the epigenetic regulation mediated by microRNA sequences. Equally, proteins involved in uptake of modified LDL are also modulated by miRNA sequences: TLR-4 by miR-21[165], miR-181a[192] and miR-223[198], LOX-1 by miR-30[170] and miR-98[176], CD36 by miR-181a[192] and miR-758[204], while LPL is targeted by miR-134[180,181] and miR-361[200] (Figure 2). Storage of cholesterol as droplets of cholesteryl ester is modified by miR-9 targeting of SOAT1[157], while cholesterol removal by autophagy is reduced by miR-17-5p dependent repression of Beclin-1[160].

Figure 2.

Key pathways involved in foam cell formation regulated by microRNA. Native low-density lipoprotein (LDL) and oxidized LDL is processed in the late endosome/lysosomes by lysosomal acid lipase, generating free cholesterol which is stored in the form of lipid droplets after esterification via acyl-CoA cholesteryl acyl transferase or sterol O-acyltransferase 1 at the endoplasmic reticulum. Cholesterol can be removed from the cell by trafficking from the late endosomes, or by hydrolysis of lipid droplets and transport to the plasma membrane to be transferred to lipid-poor apolipoprotein A-I or nascent high-density lipoprotein via ABC transporters (ATP binding cassette transporter A1, ATP binding cassette transporter G1). Inflammatory signalling pathways can be activated in foam cells via recognition of oxLDL by toll-like receptor 4 (TLR4), or by intracellular free cholesterol forming cholesterol crystals, leading to the expression and release of inflammatory cytokines. Since their initial discovery, numerous miRNA sequences have been shown to play a role in targeting each of these key steps in the formation of foam cells. For example, influx of modified lipoproteins into macrophages via oxidized low-density lipoprotein (lectin-like) receptor 1, cluster of differentiation 36 and TLR4, is reported to be regulated by miR-21, miR-30, miR-98, miR-181a, miR-223 and miR-758. The cholesterol efflux pathway is modulated by distinct sequences, including miR-19b, miR-20a/b, miR-23, miR-27a/b, mir-155 and miR-378, while miR-9 and miR-17 regulate the esterification and hydrolysis of cholesterol droplets. MicroRNA-181a regulates both lipid metabolism and inflammatory response, while let-7g, miR-146a/b, miR125b and miR-155 influence macrophage inflammatory phenotype. Dotted arrows indicate the paths for cholesterol derived from the extracellular environment within the macrophage; solid arrows indicate inflammatory signalling pathways. HDL: High density lipoprotein; ABCA1: ATP binding cassette transporter A1; ABCG1: ATP binding cassette transporter G1; ACAT-1: Acyl-CoA cholesteryl acyl transferase or sterol O-acyltransferase 1; ApoA-I: Apolipoprotein A-I; CD: Cluster of differentiation; ER: Endoplasmic reticulum; FC: Free cholesterol; IL: Interleukin; IRAK: Interleukin 1 receptor associated kinase 4; LAL: Lysosomal acid lipase; LOX-1: Oxidized low-density lipoprotein (lectin-like) receptor 1; MyD88: Myeloid differentiation primary response 88; nCEH: Neutral cholesteryl ester hydrolase; NPC: Niemann-Pick disease type C; NF-κB: Nuclear factor kappa beta; PL: Phospholipid; SR: Scavenger receptor; TLR: Toll-like receptor; TNF-α: Tumour necrosis factor alpha.

Notably, a mimic of miR-134, which enhances LPL activity and protein expression and increases macrophage cholesterol mass, also promotes the production of inflammatory cytokines[180] and increases atheroma formation in the apoE^-/- murine model of atheroma[181]. Sequences repressing ABCA1 (miR-144[182], miR-302[199]) also enhance cytokine expression; a mimic of miR-144[183] accelerates lesion development in vivo, and circulating levels of this sequence correlate with acute myocardial infarction[183], while an inhibitor of miR-302 increases aortic and hepatic expression of ABCA1 and reduces plaque size and inflammation in Ldlr^-/- mice fed a high fat diet[199].

miRNA sequences linking inflammation with cholesterol accumulation in macrophages

miRNA sequences which target the expression of proteins within cell signalling pathways mediating inflammatory responses have also been shown to reduce cholesterol accumulation in macrophages (Table 1)[153,155-204]. For instance, let-7g inhibits both canonical (RelA/p50) and non-canonical (RelB/p52) NF-κB signalling pathways, limiting inflammatory (IL-1, IL-6, MCP-1) and apoptotic responses, and decreasing macrophage foam cell formation[155] in vitro and in vivo. Further, let-7g inhibition of nuclear translocation of RelA/p50 in macrophages treated with OxLDL prevents NF-κB dependent upregulation of SREBF2 and miR-33a, and results in up-regulation of ABCA1[155]. Indeed, aberrant expression of members of the lethal-7 (let-7) miRNA family have been linked with a number of diseases, including atherosclerosis and cancer[205-207]: Reductions in expression of let-7, which can be mediated by RNA binding protein Lin-28 homolog A (Lin-28), is observed in human carotid plaques from diabetic individuals, and diabetic apoE^-/- mice[207].

miR-146a, which also targets the NF-κB pathway, inhibits the production of TNF-α by macrophages in vitro, and limits inflammation and plaque development in murine models of atheroma[184]. Plaque development and inflammation are also inhibited by miR-146a which targets the tumour necrosis factor receptor-associated factor (TRAF6)-NF-κB signalling axis[185] thought to underlie many cardiovascular pathologies[208]. Equally, the loss of miR-21, which targets mitogen-activated protein (MAP) kinase kinase 3 (MKK3) within the p38 MAP kinase pathway[166], promotes the degradation of ABCG1, reducing cholesterol removal and promoting the formation of foam cells in vitro. In vivo, deletion of miR-21 increases the number of macrophages within arterial lesions, and enhances the production of inflammatory cytokines[166]. Reductions in expression of miR-181a, which targets mitogen-activated protein kinase kinase 1 (MEK1) in the extracellular signal-regulated kinase (ERK)-1/2 pathway, have been linked to upregulation of NRLP3 inflammasome-related proteins[191], while increased expression of this sequence is associated with decreases in macrophage lipid accumulation[192].

Unsurprisingly, given their roles in regulating inflammatory responses, a number of miRNA sequences have been linked with regulating macrophage polarisation to differing phenotypes, recently reviewed by Essandoh et al[209]. Notably, miR-9, miR-125b and miR-155 are sequences linked with polarization towards the M1 phenotype[209]; miR-125b and miR-155 are induced by exposure to oxLDL in human macrophages, but mimics of miR-9 and miR-155 are linked with inhibition of foam cell formation by repression of SOAT1[157], enhanced expression of cholesteryl ester hydrolase[190], blockade of lipid uptake[189] and increased cholesterol efflux[190], suggesting divergence from the inflammation-lipid accumulation axis. Macrophages are induced to the M2 phenotype by several sequences, including miR-146a and miR-223[209]. miRNA-146a inhibits inflammatory responses in murine macrophages, and also reduces inflammation and plaque formation in murine models of atheroma[184]. Levels of miR-223 are reduced by OxLDL, and LPS, but elevated in murine atherosclerotic lesions, and overexpression of this sequence prevents both foam cell formation and production of inflammatory cytokines[198]. However, much less is known about the impact of miRNA mimics or inhibitors involved in phenotypic modulation after induction of lipid accumulation in macrophages, and whether these molecules can induce phenotypic plasticity or aid lesion regression remains a key question.

Novel and emerging pathways associated with foam cell formation

Importantly, research into microRNA sequences modulated during foam cell formation has highlighted a number of previously unrecognised pathways contributing to this process, which may also prove useful therapeutic targets (Figure 3). For example, the study of miR-155 revealed a previously unsuspected role for calcium-regulated heat stable protein 1 (CARHSP1/CRHSP-24) in foam cell formation[189]. This cytoplasmic protein, a cold shock domain (CSD) protein family member, is found within processing bodies or exosome granules, and was first identified as the physiological substrate for calcineurin (PP2B)[189,210,211]. The conserved CSD domain binds to the AU-rich element (ARE) in the 3-UTR of TNF-α, increasing mRNA stability and enhancing inflammation[210,211]. NF-κB induction of miR-155 by oxLDL in human macrophages is mirrored by increased levels in plasma and atherosclerotic lesions of patients with atherosclerosis[189]. MicroRNA-155 binds directly to the 3’-UTR of CARHSP1 to reduce expression of this protein and TNF-α in macrophage foam cells; knockdown of CARHSP1 inhibits lipid accumulation and TNF-α production, while overexpression of CARHSP1 reverses the protective effects of miR-155[189].

Figure 3.

Identification of novel pathways associated with foam cell formation. MicroRNA sequences altered during macrophage foam cell formation reveal novel pathways involved in this process, and highlight the complexity of miRNA function in targeting multiple gene pathways, exemplified here by miR-155 (Table 1). Inhibition of expression of the cell surface immunoregulatory glycoprotein, T-cell immunoglobulin and mucin-domain containing-3 (Tim-3), by miR-155 (1) increases hydrolysis of cholesteryl esters by neutral cholesteryl ester hydrolase, and promotes efflux of this lipid via ATP binding cassette transporter A1 and ATP binding cassette transporter G1, to apolipoprotein A-I and high density lipoprotein respectively. MicroRNA-155 also represses expression of the transcriptional repressor B-cell lymphoma 6 protein[236], which increases nuclear factor kappa beta activity and enhances production of the chemokine C-C motif ligand 2 (2); Repression of the cytoplasmic protein, calcium-regulated heat stable protein (CARHSP1) by miR-155, results in reduced binding of this protein to the 3’UTR of the TNFα gene transcript, and to reduced mRNA stability and decreased output of this cytokine (3); MicroRNA-155 also directly targets (represses) HMG-Box transcription factor 1, thereby increasing production of reactive oxygen species and loss of inhibition of macrophage migration inhibitory factor, leading to increased oxidatively modify proteoglycan-bound low density lipoprotein uptake and lipid accumulation (4). The black arrows represent direct targeting by miR-155; orange bars and arrows represent the functions of miR-155 targets in the absence of this miRNA sequence. HDL: High density lipoprotein; ABCA1: ATP binding cassette transporter A1; ABCG1: ATP binding cassette transporter G1; ACAT-1: Acyl-CoA cholesteryl acyl transferase or sterol O-acyltransferase 1; ApoA-I: Apolipoprotein A-I; Bcl6: B-cell lymphoma 6 protein; CARHSP1: Calcium-regulated heat stable protein; CCL2: C-C motif chemokine ligand 2; HBP1: HMG-Box transcription factor 1; MIF: Macrophage migration inhibitory factor; NF-κB: Nuclear factor kappa beta; ROS: Reactive oxygen species; TNF-α: Tumour necrosis factor alpha.

Equally, insight into the hitherto uncharacterised role of programmed cell death 4 (PDC4) in foam cell formation and atherosclerosis was revealed by investigation of the function of miR-16[159]. Expression of PDCD4, which can act as a tumour suppressor, is induced by apoptosis and is known to regulate both inflammatory and apoptotic responses[212-214]. MicroRNA-16 suppresses the activation of inflammatory macrophages by directly targeting the 3’-UTR of PDCD4[159]. Levels of miR-16 decline in macrophages treated with oxLDL and in aortic lesions of apoE^-/- mice fed a high fat diet, which also exhibit greater levels of PDCD4 protein. Either knockdown of PDCD4, or transfection with a miR-16 mimic, inhibits the expression and secretion of pro-inflammatory cytokines, and enhances expression and release of the anti-inflammatory factor IL-10, while an inhibitor of miR-16 achieves the reverse; these outcomes are also associated with modulation of ERK, p38 MAP kinase and NF-κB[212].

In other studies, the mechanism of action of molecules such as puerarin, the major bioactive ingredient isolated from Pueraria lobata and known as Gegen in traditional Chinese medicine, have been revealed by studies using miRNA[156]. Targeting the 3-UTR region of serine/threonine kinase 11 (STK11) using a miR-7 mimic, revealed that this drug enhances ABCA1-dependent cholesterol efflux via a mechanism which involves STK11 activation of AMP kinase and enhanced expression of PPAR-γ-LXR-ABCA1. Finally, it is clear that the contribution of some miRNA targets in foam cells remain to be established. For example, miR-28-5p, which is upregulated in murine macrophages treated with oxLDL, targets LDL receptor class A domain containing 3 (LRAD3)[170], but the contribution of this novel lipoprotein receptor to foam cell formation has not been investigated: At present, this protein has been linked with amyloid precursor protein trafficking in neurons[215] and with activation of E3 ubiquitin-protein ligase Itchy homolog (Itch) and E3 ubiquitin-protein ligase NEDD4 that promote proteasomal degradation[216].

Pathways targeted by miRNA sequences altered in human macrophage “foam” cells: DIANA/KEGG predictive analysis

It is increasingly recognised that networks of miRNA sequences, and their combined effects on multiple pathways, are important epigenetic determinants of complex phenotypes, just as genome-wide association studies have revealed shared genes and pathways in human disease[217,218]. The (human) sequences described in Table 1 were analysed using DIANA-miRPATH v3.0, and the miRNA versus GO/GOSlim/KEGG entries heat map is shown in Figure 4. This functionality enables identification of miRNA belonging to similar functional categories, and identification of pathways lying under the regulation of similar miRNAs[219].

Figure 4.

Pathways targeted by miRNA sequences altered in human macrophage “foam” cells: DIANA/KEGG predictive analysis. The human miRNA sequences described in Table 1 were analysed using DIANA-miRPATH v3.0, yielding a heat map of miRNA vs Gene Ontology/GOSlim/Kyoto Encyclopedia for Genes and Genomes entries.

Several well-established pathways, targeted by multiple and distinct miRNA sequences/clusters, and known to regulate vascular function and atherogenesis, emerge from this predictive analysis. These include adherens junctions, which are a key part of the common signalling network linking age-related disease proteins (ARDPs) and longevity-associated proteins (LAPs) in the human interactome[220]. The endothelial adherens junction complex, formed of vascular endothelial (VE)-cadherin and associated catenins, is a key determinant of arterial permeability, dysregulation contributing to vascular inflammation and atherosclerosis[221], while attenuating intraplaque vascular leakage reduces macrophage accumulation, necrotic core size and intraplaque haemorrhage[222]. Identification of the TGF-β signalling pathway as a target of miRNA sequences altered in macrophage foam cells is equally unsurprising, given the widely recognised, and extensively reviewed, role of this cytokine in controlling macrophage phenotype[223], atherosclerosis[224] and cardiovascular function[225].

More intriguingly, the Hippo signalling pathway emerges as highly targeted by multiple miRNA sequences implicated in foam cell formation (Figure 4); originally discovered in Drosophila and highly conserved in mammalian cells, this pathway regulates cell survival, proliferation and apoptosis[226]. Li et al[170] first showed that target genes of differentially expressed miRNA sequences are enriched in this pathway, in murine RAW264.7 macrophages treated with OxLDL; the Hippo/Yes-associated protein (YAP) signalling pathway is linked with vascular remodelling, pulmonary hypertension, aortic aneurysm, restenosis and angiogenesis, and atherosclerosis[226,227]. Notably, the atheroprotective effect of steady laminar flow in major arteries is linked with inhibition of Hippo/YAP effector function[228] while activation of this pathway is linked with vascular remodelling, and switching of arterial smooth muscle cells to the “synthetic” proliferative phenotype in response to biochemical stretch[229]. The effector function of YAP is linked with accelerated atherosclerosis in apoE^-/- mice[230], while the herbal extract Scutellarin can protect against atherosclerosis in rats by modulating the Hippo-YAP-Forkhead box (FOXO)3A transduction pathway[231].

Another pathway enriched in targets of multiple miRNA sequences is that involved in bacterial invasion of epithelial cells (Figure 4). Infection and systemic inflammation are linked with atherogenesis in a number of epidemiological studies[232] and vascular cells and macrophages are subject to invasion by bacteria via a number of mechanisms, including evasion of autophagy and internalisation via lipid rafts. In turn, this has led to the notion of vascular tissue providing a “privileged niche” in which bacteria can persist in dormancy for extended periods of time before becoming activated in phagocytic cells, contributing to the chronic and unresolved inflammation which characterises atherosclerosis[232]. The epigenetic miRNA profile found in macrophage “foam” cells which may modulate susceptibility to bacterial invasion may also suggest key proteins (and pathogens) implicated in this process, and/or highlight possible therapeutic strategies designed to limit the impact of vascular “infectology”[232].

THERAPEUTIC OPTIONS: CLINICAL APPLICATIONS OF MIRNA (TARGETS)

miRNA pathways are excellent candidates for pharmacological manipulation, and have been invoked as biomarkers, diagnostics or therapeutics for a number of disease conditions[140,233,234]. For example, Caruso et al[233] monitored dynamic changes in microRNA profiles in lung tissue during the development of pulmonary arterial hypertension (PAH) in hypoxic rodents. The same authors discovered that miR-145 is a useful indicator of hypoxia in mice, and of heritable and idiopathic pulmonary arterial hypertension in patients; down-regulation of miR-145 also had utility in protecting against development of PAH in mice[234]. Further, the “ThyraMIR” testing platform, which examines the expression of a panel of ten miRNA in conjunction with selected disease-associated genes, has been approved for diagnostic use in thyroid cancer when malignancy risk cannot be determined by conventional cytology[235].

Treatments involving miRNAs focus on the concept of specifically influencing levels of miRNAs in certain diseases – including suppression of miRNAs, as well as raising miRNA levels or substituting artificially generated copies[140]. Mimics can be used for gene silencing, by generating artificial, double-stranded miRNA-like RNA fragments, which bind specifically to target mRNA, activating the RISC complex; this results in down-regulation of specific mRNAs and gene suppression (above). Equally, chemically engineered oligonucleotides are capable of silencing single endogenous miRNAs, binding to the target mature miRNA, leading to reduced activation of RISC and up-regulation of specific mRNAs and gene expression. Other approaches involve “target mimicry” using miRNA sponges, masking or erasers[140].

Delivery of disease-specific miRNA mimics or inhibitors remains in the developmental stage with multiple miRNA therapeutics currently in clinical trials. The most advanced trial, currently in Phase II, employs a chemically engineered inhibitor for miR-122 (Miravirsen) which, under normal conditions, binds to the 5’-UTR region of the hepatitis C virus and enhances its transcription[236-243]. By hybridizing to mature miR-122, Miravirsen has been shown to effectively inhibit viral replication with minimal “off target” effects[236-239]. MicroRNA-based clinical trials are also underway for the development of novel treatments for various cancers. Currently in Phase I and Phase II trials, the efficacy of an inhibitor (MRG-106) targeting miR-155 is being investigated for treatment of a variety of lymphomas, reflecting the recognised role of this sequence in driving malignant lymphocyte proliferation[240,241].

Despite the encouraging progression of miRNA therapies, significant challenges have also been highlighted in some clinical trials. One such promising miRNA therapeutic, the miR-34 mimic “MRX34”, was employed in a Phase I trial for patients with advanced liver cancer[242-244]; despite dose-dependent modulation of miR-34 target oncogenes, the study was halted due to serious adverse effects in a small cohort of subjects[242-244]. This study also highlighted a challenging area for the development of miRNA-based therapies: The preclinical studies demonstrated that the liposomal delivery system resulted in elevated miR-34 in multiple tissues in non-human primates[244]. While this may be beneficial for miRNA therapeutics used to treat diseases that can arise in several anatomical locations, in the case of tissue specific diseases, such as atherosclerosis, site-specific homing could dramatically reduce potential off-target effects.

To overcome this issue, liposomes enriched in specific amino acid sequences have been developed which result in increased tissue-specific accumulation. The efficacy of this system, for the delivery of short, siRNA, has been demonstrated in vivo in osteoporotic mice[245]. Use of a lipid nanoparticle containing C-C chemokine receptor type 2 (CCR2)-targeting siRNA resulted in high levels of localisation in bone marrow and spleen, significant reductions in monocyte CCR2 expression, decreased myeloid cell infiltration in the plaque and an overall reduction in lesion size in ApoE^-/- mice[246]. While this system targets atherosclerotic plaque indirectly, additional delivery mechanisms have been employed in animal studies that may facilitate plaque-directed delivery of miRNA-based therapeutics. Notably, reconstituted HDL (rHDL) can act as a carrier particle for delivery of drugs and microRNA: In ApoE^-/- mice, rHDL was used to delivery simvastatin to plaque regions, resulting in reduced local inflammation[247], while miR-223 incorporated into rHDL in vitro was able to selectively target cells expressing SR-BI[148].

Thus, many factors need careful consideration in developing miRNA therapeutics for atherosclerosis, including effective vectors and delivery options, and the nature of “off-target” side-effects and/or toxicities which may occur due to disruption of multiple target genes and/or cell signalling networks[248,249]. However, since differing microRNA sequences impact on distinct stages of the atherogenic process[248,249], delivery of a pool of mimics and/or inhibitors may be an attractive therapeutic strategy for treatment of this complex, multicellular disease[248,249]. Defined stages of the disease process could be targeted by distinct miRNA mimics/inhibitors, predicated by serum levels of secreted miRNA sequences. Such approaches, if fully validated, might be used to provide personalised treatment, or be beneficial in targeting asymptomatic patients, or those in whom statin use is contraindicated or ineffective[250-252].

CONCLUSION

Huge advances have been made in understanding the epigenetic factors, and particularly the role of small non-coding miRNA sequences, in regulating macrophage “foam” cell formation and function over the last decade. Networks of genes regulated by multiple miRNA sequences have been revealed, and new pathways discovered which contribute to the atherogenic process, which may ultimately lead to RNA-based therapeutics capable of preventing or regressing the formation of complex atherosclerotic lesions by targeting macrophage function.