Downstream effects of endocannabinoid on blood cells: implications for health and disease

Abstract

Endocannabinoids (eCBs), among which N-arachidonoylethanolamine (AEA) and 2-arachidonoylglycerol (2-AG) are the most biologically active members, are polyunsaturated lipids able to bind cannabinoid, vanilloid and peroxisome proliferator-activated receptors. Depending on the target engaged, these bioactive mediators can regulate different signalling pathways, at both central and peripheral levels. The biological action of eCBs is tightly controlled by a plethora of metabolic enzymes which, together with the molecular targets of these substances, form the so-called “endocannabinoid system”. The ability of eCBs to control manifold peripheral functions has received a great deal of attention, especially in the light of their widespread distribution in the body. In particular, eCBs are important regulators in blood, where they modulate haematopoiesis, platelet aggregation and apoptosis, as well as chemokine release and migration of immunocompetent cells. Here, we shall review the current knowledge on the pathophysiological roles of eCBs in blood. We shall also discuss the involvement of eCBs in those disorders affecting the haematological system, including cancer and inflammation. Knowledge gained to date underlines a fundamental role of the eCB system in blood, thus suggesting that it may represent a therapeutic promise for a broad range of diseases involving impaired hematopoietic cell functions.

The endocannabinoid (eCB) system

The endocannabinoid (eCB) system includes: (1) a group of bioactive lipids released from membrane phospholipid precursors, named eCBs, (2) their metabolic enzymes, and (3) their target receptors [1, 2]. Briefly, these components, depicted in Table 1, will be described later.

Table 1.

The main elements of the eCB system

Member	Description	Function	References
Bioactive lipids
AEA	Derivatives of ω6 PUFA	They bind CB receptors, and act in the central nervous system and in the periphery	[1, 2]
2-AG
2-AGE
Virodhamine
NADA
EPEA	Derivatives of ω3 PUFA
DHEA
PEA	eCB-like compounds	They do not bind CB receptors, but potentiate eCB function	[3]
OEA
Metabolic proteins
EMT	Trans-membrane transporter	Responsible for AEA (and possibly for the other eCBs) transport	[9]
NAPE-PLD	Biosynthetic enzymes	Responsible for AEA synthesis	[4, 5]
ABHD4
PLC
DAGL		Responsible for 2-AG synthesis
FAAH-1	Hydrolytic enzymes	Responsible for AEA hydrolysis	[4, 10]
FAAH-2
NAAA
MAGL		Responsible for 2-AG hydrolysis
ABHD6
ABHD12
Target receptors
CB1	Cannabinoid receptors	Main targets of eCBs	[12–14, 16]
CB2
GPR55		Novel target of eCBs
TRPV1	Vanilloid receptor	Target of AEA and congeners	[19, 20]
PPAR α and γ	Peroxisome proliferator-activated receptors	Targets of eCBs	[21]

AEA arachidonoylethanolamine, 2-AG 2-arachidonoylglycerol, 2-AGE 2-arachidonoylglycerylether, NADA N-arachidonoyldopamine, EPEA N-eicosapentaenoylethanolamine, DHEA N-docosahexaenoylethanolamine, PEA N-palmitoylethanolamine, OEA N-oleoylethanolamine, EMT endocannabinoid membrane transporter, NAPE-PLD N-acyl-phosphatidylethanolamines-hydrolyzing phospholipase D, ABHD serine a/b-hydrolase, PLC phospholipase C, DAGL diacylglycerol lipase, FAAH fatty acid amide hydrolase, NAAA N-acylethanolamine-hydrolyzing acid amidase, MAGL monoacylglycerol lipase, CB cannabinoid, TRPV1 transient receptor potential vanilloid 1, PPAR peroxisome proliferator-activated receptor, PUFA polyunsaturated fatty acid

The eCB family includes amides, esters and ethers of long-chain polyunsaturated fatty acids (PUFAs), among which the best characterized members are N-arachidonoylethanolamine (anandamide, AEA) and 2-arachidonoylglycerol (2-AG), both derivatives of arachidonic acid [1]. Beside eCBs, our body synthesizes eCB-like compounds [including N-palmitoylethanolamine (PEA) and N-oleoylethanolamine (OEA)] that exert their effect without binding cannabinoid receptors, and potentiate eCB function by inhibiting their degradation [3].

Both AEA and 2-AG are produced “on demand” through multiple biosynthetic pathways, which reflect the variety of physiological stimuli (including neuronal activity, glucocorticoids, insulin and cytokines) able to mobilize these eCBs [4–8]. The in–out and out–in movement of eCBs across the plasma membrane is a not yet fully elucidated process and several hypotheses have been proposed: (1) passive diffusion, (2) facilitated transport via a specific carrier called eCB membrane transporter (EMT), and (3) caveolae-mediated endocytosis [9]. The biological activity of eCBs is ended by hydrolysis catalysed by multiple enzymes or isozymes; the main hydrolases responsible for AEA breakdown into arachidonic acid and ethanolamine are fatty acid amide hydrolase- (FAAH-) 1 and 2 and N-acylethanolamine-hydrolyzing acid amidase (NAAA), while 2-AG is converted to fatty acid and glycerol by monoacylglycerol lipase (MAGL), FAAH, a/b-hydrolases (ABHD) 6 and 12 [4, 10]. Finally, both AEA and 2-AG can originate oxidative derivatives, by the action of lipoxygenases, cyclooxygenase-2 and cytochrome P₄₅₀ (Fig. 1) [11].

Fig. 1.

Oxidative metabolism of AEA (a) and 2-AG (b). 12-LOX 12-lipoxygenase, COX-2 cyclooxygenase-2, cytP ₄₅₀ cytochrome P_450, 12-HAEA 12-hydroxyeicosatetraenoylethanolamide, PGE ₂ -EA prostaglandin E₂-ethanolamide, 5,6-EET-EA 5,6-epoxyeicosatrienoic acid-ethanolamide, 12-HETE-G 12-hydroxyeicosatetraenoyl-glycerylester, PGE ₂ -GE prostaglandin E₂-glycerilester, 5,6-GEET 5,6-glycerated epoxyeicosatrienoic acid

The different signalling pathways activated by AEA and 2-AG strictly depend on the specific receptor engaged. To date, three G protein-coupled receptors (GPRs) have been shown to bind eCBs: (1) type-1 (CB₁) cannabinoid receptor highly expressed in brain, but also in lung, liver and kidney, as well as in T lymphocytes and platelets [12–14], (2) type-2 (CB₂) receptor, mainly present in the immune system and in haematopoietic cells [12, 15], and (3) GPR55, ubiquitously expressed and involved in modulation of processes related to cardiovascular system and inflammation [16–18]. AEA, but not 2-AG, is also an agonist of the transient receptor potential vanilloid 1 (TRPV1) channel, expressed in primary sensory neurons and peripheral cells; by activating TRPV1, AEA triggers pro-apoptotic signalling pathways, and exerts a physiological control of brain functions [19, 20]. Additional targets of eCBs are the peroxisome proliferator-activated receptors (PPARs) α and γ, through which eCBs regulate adipocyte differentiation, lipid and glucose metabolism, as well as inflammatory responses [21].

In the next sections, we will describe the knowledge gained so far on the role of eCB system in generation and function of haematological cells. Without seeking to be exhaustive, we will focus on few selected examples of blood physiology and pathology.

The eCB system and haematopoiesis

Haematopoiesis is a complex and highly ordered differentiation and self-renewal process, through which blood cells are produced from haematopoietic stem cells (HSCs), a population of multipotent cells residing in bone marrow of adult mammals [22]. HSC retention in bone marrow niches (homing) or mobilization is allowed by specific transcription factors, cytokines [including stromal-derived factor-1 (SDF-1)] and growth factors [including interleukin-3 (IL-3), granulocyte–macrophage colony-stimulating factor (GM-CSF), granulocyte colony-stimulating factor (G-CSF), erythropoietin, and macrophage colony-stimulating factor (M-CSF)] [23–25].

eCBs can be counted among factors governing hematopoietic stem cell biology. Stromal cells, in fact, release significant amounts of eCBs (whose levels also increase during inflammation), which exert distinct effects on HSC differentiation and migration, alone or in synergy with classical growth factors [26–28]; eCB effects on clonal cell expansion and mobilization are mainly achieved through activation of CB₂ receptor, highly expressed in human and murine HSCs (Table 2) [26, 27, 29–32]. Not only eCBs (and especially 2-AG) control HSC self-renewal and proliferation, but they are also involved in lineage commitment and differentiation of distinct cell populations. Studies performed in our laboratories indicated that 2-AG was able to drive a bipotential cell line (expressing surface antigens of both erythroid and megakaryocytic phenotypes) towards megakaryocytic differentiation; the eCB, indeed, enhanced expression of megakaryocyte/platelet surface antigens (including β3 integrin subunit and glycoprotein VI), while it reduced the expression of erythroid markers, such as glycophorin A [33]. We recently found that 2-AG was also able to complete megakaryocytic differentiation, by stimulating platelet generation and release, thus potentially having clinical efficacy to counteract thrombocytopenia-associated diseases [34]. Noticeably, we observed that cells drop down the synthesis of this lipid mediator at the end of differentiation, thus indicating that they are able to self-regulate 2-AG levels, and thus pro-differentiating stimuli [33, 34].

Table 2.

Effects of CB₂ agonists on haematopoiesis

Compound	Clonal expansion	Migration	References
AEA	+	−	[27, 29]
2-AG	+	+	[27, 30, 31]
PEA	−	+	[27]
AM1241	=	+	[26]

+, stimulation; −, inhibition; =, no effect

Although further work is needed, the finding that eCBs can be listed among key drivers of hematopoiesis might broaden the field of investigation; targeting the eCB actions should be helpful to manage bone marrow failure and blood cell loss occurring in several pathological conditions.

The eCB system and blood cells

Erythrocytes

To date, only a few data are available on erythrocytes. Using human red blood cell ghosts, Bojesen and Hansen [35] demonstrated that AEA quickly (within seconds) crosses erythrocyte membranes via a saturable mechanism that does not require ATP. At concentrations higher than those found in circulating plasma of healthy individuals, AEA is oxygenated by cyclooxygenase and generates PGE₂, with profound effects on erythrocyte survival. Indeed, PGE₂ activates Ca²⁺-permeable channels, thus triggering Ca²⁺-sensitive K⁺ channels, water loss and cell shrinkage, accompanied by phosphatidylserine exposure and engulfment of erythrocytes by macrophages [36]. Such an effect may have therapeutical implications, as suggested by Bobbala and colleagues [37]. Indeed, AEA enhances cell death and decreases in vitro parasitaemia of Plasmodium falciparum-infected human erythrocytes, while in vivo administration blunts parasitaemia and enhances survival of Plasmodium berghei-infected mice (Fig. 2). Overall, by exerting a direct toxic effect on the pathogen and by enhancing cell death and rapid clearance of infected erythrocytes, AEA counteracts the lethal course of the disease [37].

Fig. 2.

Schematic representation of different effects of (e)CBs on blood cells. 1 AEA enhances cell death of infected erythrocytes. 2 (e)CBs exert immunosuppressive effects by inhibiting lymphocyte proliferation and/or inducing apoptosis, as well as inhibiting pro-inflammatory cytokine release. They also control the balance among specific subsets of T cells. 3 Either 2-AG [released from platelet-activating factor (PAF)-stimulated macrophages and platelets] or AEA [produced from lipopolysaccharide (LPS)-stimulated macrophages] induces vasodilation during septic shock. 2-AG also stimulates macrophage phagocytic activity; some eCBs suppress release of pro-inflammatory mediators from activated macrophages. 4 (e)CBs inhibit neutrophil recruitment into inflamed tissues and secretion of pro-inflammatory mediators. Otherwise, they can promote the neutrophil adhesion cascade. 5 2-AG induces platelet aggregation, while AEA prolongs platelet life span. See text for further details

Leukocytes

eCB signalling through CB receptors has been proved to modulate homoeostatic immune balance, affecting the biological activity of all types of white blood cells. The ability of eCBs to influence both humoral and cellular immunity is an ever-increasing area of cannabinoid research; given the complexity of the relationship between eCBs and immune system, we refer to other articles providing a more comprehensive overview [38, 39], here highlighting only some aspects of this topic.

All subsets of lymphocytes express CB receptors, with the CB₂ subtype being the most abundant, and expression levels are related to activation state [40]. In addition, message levels are highest in B cells, followed by NK, T8 and T4 cells [41]. B cell proliferation, migration and Ig production are modulated by eCBs, which preferentially act on naïve B cells, thus modulating B cell compartments in spleen and secondary lymphoid tissues [30, 41–44]. Concerning T lymphocytes, eCB generally mediates immunosuppression via at least four different pathways (Fig. 2): (1) inhibition of transcription factors and suppression of cytokine production [45–48], (2) inhibition of proliferation [48], (3) induction of apoptosis [49]; (4) induction of specific subsets of T cells (especially by modulating T helper (Th) 17/T regulatory and Th1/Th2 ratios) [48–51]. In this context, it should be noted that eCB tone is modulated by Th1/Th2 balance: lymphocyte treatment with the Th2 cytokines IL-4 or IL-10 stimulates FAAH expression and activity, whereas the Th1 cytokines IL-12 and interferon (IFN) γ inhibit it [52].

The presence of eCB elements has been documented in both immortalized and primary circulating macrophages, at transcriptional, translational and functional levels. These cells, indeed, possess all proteins to bind and to metabolize both AEA and 2-AG [53–55], although these proteins are differentially regulated upon stimulation. Indeed, RAW264.7 cells and mouse peritoneal macrophages treated with lipopolysaccharide (LPS) show increased AEA levels, due to activation of its biosynthetic enzyme, N-acylphosphatydiletanolamine phospholipase D (NAPE-PLD). Instead, 2-AG cellular levels are unaffected by LPS, although they are sensitive to treatment with platelet-activating factor [56]. These findings indicate that both AEA (produced by activated macrophages) and 2-AG (secreted from activated platelets and macrophages) may be paracrine mediators of endotoxin-induced hypotension [56, 57] (Fig. 2). Several reports documented inhibition of macrophage functions by eCBs. AEA has been proven to inhibit (1) macrophage-mediated killing of tumour necrosis factor α (TNFα)-sensitive murine fibroblasts [58], (2) NO production by LPS-activated mouse peritoneal macrophages [59] and (3) release of pro-inflammatory cytokines (TNFα, IL-4, -6, -8, IFNγ) by human monocytes [60]. PEA shows inhibitory effects similar to those of AEA, except for a lack of effect on monocyte-dependent TNFα production and lymphocyte-dependent IFNγ synthesis [60]. Overall, a selective action of the two eCBs (maybe at receptor level) and a strict dependence on eCB tone [60] might account for these observations. 2-AG has been shown to inhibit TNFα secretion from LPS-treated mouse macrophages [61], as well as NO, PGE₂ and IL-6 release from J774 macrophages through CB₂ activation [62]. Unlike AEA, 2-AG seems to play an essential role in the recruitment of inflammatory and immunocompetent cells. Indeed, upon 2-AG treatment, undifferentiated HL-60 cells, as well as HL-60 cells differentiated into macrophage-like cells, showed enhanced IL-8 and macrophage-chemotactic protein 1 (MCP-1) production [63], paralleled by actin polymerization and extension of pseudopods [64]. Furthermore, differentiated HL-60 cells showed enhanced phagocytosis of opsonized zymosan in the presence of 2-AG; CB₂ receptor, phosphoinositide 3kinase (PI3K) and extracellular signal-related kinase (ERK) were suggested to be involved in these effects [65] (Fig. 2). Once activated by invading microorganisms, immunocompetent cells led to elevated 2-AG levels in inflamed tissues, therefore it is tempting to speculate that 2-AG may stimulate (in an autocrine and/or paracrine fashion) the phagocytic activity of other types of inflammatory cells, thus contributing to self-defence mechanisms against infection.

Finally, our group has recently demonstrated an oxLDL-dependent modulation of the eCB system in primary human macrophage-derived lipid-loaden foam cells. Indeed, foam cells showed: (1) increased FAAH activity, (2) triplicated AEA levels, (3) doubled CB₁/CB₂ binding activity, (4) reduced TRPV1 binding activity [55]. These data, together with the finding that selective activation of CB₂ receptor reduced cellular oxLDL uptake and cytokine (namely, TNFα, IL-12 and IL-10) release by human macrophages [55], seem to speak in favour of a crucial role for the eCB system during foam cell formation.

Data on eCBs and granulocytes are quite few or controversial, and mainly concern neutrophils. Once activated by a gradient of chemotactic factors [e.g. the bacterial product formyl-Met-Leu-Phe (fMLP), and host-derived products, like IL-8 and leukotriene B₄ (LTB₄)], neutrophils are the first inflammatory cells that rapidly migrate and infiltrate tissues, to phagocyte and destroy disease-producing pathogens [66]. Despite the numerous studies, yet it is not well defined the role that eCBs play in neutrophil function, since conflicting results have been obtained. Controversial literature data may be explained, at least in part, by different experimental paradigms simultaneously supporting direct and indirect effects. Indeed, Balenga and co-workers [67] showed that l-α-lysophosphatidylinositol (LPI), the natural GPR55 agonist, stimulated cytoskeleton remodelling, as well as neutrophil polarization and migration, with a possible cooperation between GPR55 and CB₂ receptors, while McHugh and colleagues [68] reported a GPR55-mediated inhibition of migration. Moreover, CB₂ activation has been shown to prevent neutrophil release of matrix metalloprotease-9 (MMP-9) both in vivo and in vitro [69]; conversely, 2-AG stimulates chemotaxis, myeloperoxidase release, ERK1/2 phosphorylation and Ca²⁺ mobilization in freshly isolated human neutrophils, via de novo biosynthesis of LTB₄ [70].

eCBs can also interfere in the crosstalk between leukocytes and endothelial cells, in response to chemotactic stimuli released from inflamed endothelium (Fig. 2). For example, 2-AG upregulates the expression of selectins in human endothelial cells, which release TNF-α able to recruit lymphocytes and stimulate their rolling activity, thus allowing a coordinated action between the two cell types [71]. On the contrary, several findings pointed out the negative role played by CB₂ receptors on interactions between endothelial and inflammatory cells: indeed, activation of CB₂ receptor by specific agonists has been shown to decrease the amount of trans-migrating neutrophils in both myocardial and hepatic ischemia–reperfusion models [72, 73]. CB₂ activation also reduces the number of neutrophils in ischemic brain, and inhibits their migration induced by CXCL2, as well as their adhesion to brain endothelial cells; therefore, selective CB₂ activation may play a protective role against neuroinflammation, by suppressing leukocyte-blood brain barrier interactions [74, 75]. Targeting endothelial CB₂ receptor has been suggested to represent a novel strategy for treatment of atherosclerosis, as it attenuates inflammatory responses in in vitro human coronary artery endothelial cells, as well as in isolated aortas and vascular endothelium [76]. Finally, CB₂ activation may be useful to limit the progression of HIV-1 infection in the central nervous system, by inhibiting viral replication in infiltrating monocytes/macrophages [77].

Platelets

Among blood cells, platelets represent an important source of circulating eCBs, especially of 2-AG, which may participate in several pathophysiological responses. First evidence for the production of eCBs was presented by Varga and co-workers [57], who demonstrated that rat platelets contained significant amounts of 2-AG, that increased after in vitro exposure to an inflammatory stimulus. In the same year, Edgemond and colleagues [78] reported that human platelets were able to incorporate AEA and oxygenate it at the 12 position via the lipoxygenase pathway, thus producing the oxygenated derivative 12(S)-HAEA. The latter compound was able to bind both CB₁ and CB₂ receptors and to inhibit FAAH activity, thus prolonging AEA lifetime in the bloodstream. Later on, our group and others provided further biochemical evidence of eCB metabolism and their role in platelet physiology [79–82]. It is now widely accepted that platelets are able to metabolize both AEA and 2-AG, thus controlling their biological activity within the cardiovascular system.

AEA and 2-AG do not act as interchangeable mediators, but they are endowed with distinct biological functions, especially in megakaryocyte/platelet biology (Fig. 2). Although both eCBs can be involved in platelet activation [83], nonetheless only 2-AG is a true agonist of human platelets [84], while AEA more likely acts as a co-agonist, synergizing with classical inducers, such as collagen, ADP and thrombin. Indeed, 2-AG activates platelets at micromolar concentrations, by eliciting common metabolic responses (including increase in cytosolic calcium, inositol-1,4,5-trisphosphate and thromboxane A₂, and decrease in cyclic AMP), through a p38MAPK/cPLA₂-dependent mechanism [85, 86]. Activation induced by 2-AG is also accompanied by shape change, resulting from rearrangement of actin cytoskeleton: in the presence of 2-AG, changes in the G/F (i.e. monomeric/polymeric) actin ratio within platelet cytoplasm could be seen, leading to increased formation of actin filaments and cell protrusions [84]. In platelets, 2-AG also increases activity of endothelial nitric oxide synthase (eNOS), by promoting eNOS Ser1177 phosphorylation by protein kinase C, and Thr495 dephosphorylation via a mechanism involving the Ser/Thr protein phosphatase 1 [87] (Fig. 3a).

Fig. 3.

The “Yin-Yang” role of 2-AG and AEA in platelets. a Role of 2-AG as migrating factor. 2-AG activates platelets in a CB₁/CB₂ dependent manner, (1) by increasing cytosolic Ca²⁺, IP₃ and TXA₂ and decreasing cAMP, and (2) by stimulating eNOS activity. 2-AG might also be taken up by platelets and hydrolyzed by MAGL into AA, which, in turn, is oxidized by COX-1 to TXA₂. b Role of AEA as survival factor. AEA enhances platelet life span (1) by activating the survival kinase Akt, which regulates, through phosphorylation of Bad, the interactions among pro- and anti-apoptotic members of Bcl-2 family, and (2) by stimulating eNOS activity. NO might also stimulate AEA uptake, thus modulating its action. See text for further details. AA arachidonic acid, CBR cannabinoid receptor, eNOS endothelial nitric oxide synthase, cAMP cyclic AMP, COX-1 cyclooxygenase-1, IP ₃ inositol-1,4,5-trisphosphate, NO nitric oxide, MAGL monoacylglycerol lipase, TXA ₂ thromboxane A₂, PKC protein kinase C, PP1 protein phosphatase 1

Unlike 2-AG, AEA activates platelets at millimolar concentrations and at micromolar concentrations is effective only in the presence of other physiological agonists [79]. Therefore, the role of AEA is other than platelet activation and aggregation. Indeed, we demonstrated that AEA in blood may be one of the factors required for platelet survival; we reported that this eCB was able to prolong platelet life span by modulating the Akt-dependent phosphorylation of Bad, thus preventing its binding to Bcl-xL, and hence its pro-apoptotic activity [88]. Furthermore, by the same PI3K/Akt signalling pathway, AEA stimulates eNOS activity, thus increasing platelet nitric oxide (NO) and cyclic GMP basal levels [89] (Fig. 3b). The AEA-mediated NO increase may contribute to platelet survival and account for beneficial effects produced by this eCB, including vasodilatation [89, 90]. Keeping in mind that NO enhances AEA uptake (Fig. 3b) [91], an autocrine loop may be established, to remove AEA from extracellular space, thus limiting abnormal thrombus formation [79].

Although the relevance of eCBs as (co-)agonists of human platelets is now widely accepted, the role of CB receptors, as well as the mechanism of action, is controversial [92]. Our group and others [80, 85, 86, 93] showed that 2-AG-triggered aggregation is CB₁/CB₂-dependent (Fig. 3a), because it was reversed by CB₁ and CB₂ antagonists. Coherently, in unstimulated whole blood, the CB₁ antagonist rimonabant decreased P-selectin and glycoprotein IIb/IIIa surface expression (thus reducing fibrinogen binding), and thrombin-induced platelet aggregation [86]. In contrast, Braud and colleagues [81] reported that, in rabbit platelets, AEA-induced aggregation was completely prevented by inhibition of cyclooxygenase-1 and FAAH activity, and so did Keown and co-workers [92], thus supporting that eCB action occurs via release of arachidonic acid. This hypothesis has recently been sustained also by Brantl and colleagues [94], who found that 2-AG and virodhamine (but not AEA) induced human platelet aggregation in their physiological milieu, i.e. blood and plasma, as well as shape change, aggregation and ATP secretion in platelet-rich plasma, through a MAGL-dependent mechanism leading to arachidonic acid release and its subsequent metabolism to thromboxane A₂ by cyclooxygenase-1/thromboxane synthase (Fig. 3a). As we recently assessed [95], differences in experimental approaches might account for discrepancies among data concerning eCB effects on platelets. Moreover, taking into account that: (1) eCBs are metabolized by specific biosynthetic and degradative enzymes [4, 10] that control their activity at both central and peripheral levels, including in platelets [79–82]; and (2) inhibitors employed by Brantl’s group [94] to inhibit cyclooxygenase and MAGL activities have been used at significantly high concentrations, it is too simplistic to consider eCBs as a simple source of arachidonic acid, rather than true platelet (co)-agonists. Indeed, if arachidonic acid was the main player of eCB signalling, one might predict that AEA is also effective, since platelets promptly cleave it into arachidonic acid [79]. But, besides the recent study from De Angelis’ group [96] that reported an AEA-dependent inhibition of platelet aggregation and α-granule release by collagen, it is well recognized that AEA is unactive as platelet agonist [79, 80, 94]. In this context, it should also be underlined that 2-AG itself is a substrate of cyclooxygenases and lipoxygenases (see Fig. 1), being converted in biologically active oxygenated derivatives [11]. Hence, the effect of acetylsalicylic acid (inhibitor of cyclooxygenase activity) reported by Brantl’s group [94] might reflect blockade of 2-AG oxidation rather inhibition of the conversion of 2-AG-derived arachidonic acid into thromboxane A2. In conclusion, the effects of such inhibitors should be interpreted with caution and more work has to be done to unravel the molecular details of eCBs–platelet interactions.

Incidentally, human platelets express authentic CB₁ and CB₂ receptors, as we have recently demonstrated [14]. By analysing protein levels, cellular localization and functionality, we provided direct experimental evidence that both receptor subtypes are expressed in highly purified human platelets; however, they are predominantly confined inside platelets, thus explaining why only a small portion of CB₁ and CB₂ might be detected in preparations of plasma membranes [14].

Further studies are clearly warranted, especially considering the clinical potential of CB₂ agonism or CB₁ antagonism as additional therapeutic targets to reduce cardiovascular risk, where cyclooxygenase inhibitors cannot be chosen.

The eCB system in blood cell cancer

Oncogenesis, proliferation, migration and apoptosis of tumour cells are connected, in some way, to an altered eCB tone [97, 98]. However, it is not clear the exact role of eCBs in cancer-related events, neither it is known whether alterations in eCB system are one of the cancer-promoting factors or rather a consequence of generalized altered metabolism. Indeed, the ability of eCBs to activate more than one molecular target allows to trigger different (and sometimes opposite) signalling pathways, so that protective or oncogenic effects may vary according to the type of cancer, and to the activated receptor (CB₁ versus TRPV1) [99].

Overexpression of CB receptors has been reported in different blood cancer types (Table 3). Increased CB₂ levels have been found in human myeloid leukaemia cell lines, in human blasts from acute myeloid leukaemia (AML), and in certain non-Hodgkin’s B and T lymphomas [100–102]. Moreover, the finding that the majority of non-Hodgkin’s B lymphomas [101], as well as of Hodgkin’s lymphomas [103], also have increased levels of CB₁ receptor strongly suggests the involvement of this receptor in tumorigenesis.

Table 3.

Alterations of blood eCB system in pathological conditions

Pathology	Up-regulation	Down-regulation	Agonist	Effect	References
Blood cancer
Acute myeloid leukaemia	CB2				[100]
Non-Hodgkin’s B lymphoma	CB1, CB2		WIN55212-2, Met-AEA, rimonabant	↑Cell death, ↓ proliferation	[101, 104–107]
Non-Hodgkin’s T lymphoma	CB2				[102]
Hodgkin’s lymphoma	CB1				[103]
Neurological diseases
Huntington’s disease	AEA	FAAH			[136]
Multiple sclerosis	AEA, CB2 NAPE-PLD	FAAH			[137–139]
Parkinson’s disease	AEA	FAAH			[135, 143]
Alzheimer disease	FAAH				[144]
Migraine	FAAH, EMT	AEA			[150]
Chronic/medication-overuse headache		FAAH, EMT AEA, 2-AG			[151, 153]
Psychiatric disorders
Attention-deficit/hyperactivity disorder	AEA	FAAH			[145]
Depression	AEA, 2-AG				[146]
Schizophrenia			Cannabidiol	↑ AEA, improvement of symptoms	[147]

An interesting finding is that CB₂ receptor acts as a protooncogene involved in leukemic transformation in AML, while it plays a protective role against abnormal cell growth in certain B cell malignancies (Table 3) [30, 31, 100]. In mantle cell lymphoma, Gustafsson and co-workers [101, 104, 105] demonstrated that CB₂ pharmacological activation (by WIN55212-2 or Met-AEA) reduces cell proliferation via CB-dependent ceramide accumulation and p38-dependent activation of caspase-3. As demonstrated by Wasik and co-workers [106], other mechanisms, including CB-independent cytoplasmic vacuolation, may induce cell death in certain types of primary mantle cell lymphoma. Mantle cell lymphoma proliferation can be blocked also by rimonabant (a CB₁ antagonist/inverse agonist), thus suggesting that more complex mechanisms underlying CB-dependent cell growth inhibition exist [101]. Similarly, rimonabant has been shown to regulate proliferation of other types of blood cancers, where it induces cell cycle arrest or cell death responses (e.g. inhibition of PI3K/Akt pathway, phosphatydilserine exposure and dissipation of mitochondrial membrane potential) depending on the cell type considered [107].

Finally, it should also be underlined that pharmacological targeting of CB receptors might represent a novel therapeutic approach to restore blood cell functions compromised by chemo- and radiation therapies. Following sublethal irradiation, haematopoietic recovery is significantly enhanced in mice treated with AM1241 (a CB₂ agonist), via inhibition of apoptosis and promotion of cell cycle entry of HSCs, while it is impaired in CB₂ knockout mice [26].

The eCB system in inflammatory diseases

The ability of eCBs to modulate immunocompetent cells is receiving growing interest in scientific community, especially in the light of the impact on inflammatory diseases. Indeed, tissue-specific dysregulated eCB tone, resulting from altered expression of CB receptors and/or eCB metabolizing enzymes, has been reported in numerous pathological conditions. As the pathological role of the eCB system in inflammatory pathologies has been summarized in more detail elsewhere [38, 108], here we reported only few selected examples (Table 3).

(e)CBs have been shown to reduce inflammatory hyperalgesia, either in animals or humans [109–112]. In this context, it should be recalled that FAAH modulates the eCB tone, in vivo; this finding is supported by the evidence that, in λ-carrageenin treated rats, increased FAAH expression (paralleled by decreased AEA, 2-AG and PEA concentrations and enhanced CB₁ and CB₂ receptor expression) was associated to granuloma formation, while its pharmacological blockade reduced TNFα release and granuloma-dependent angiogenesis [113].

In inflammatory bowel disease (IBD), inflamed mucosa has low AEA levels, as a result of decreased biosynthesis and increased degradation [114]. Accordingly, the not-hydrolysable analogue Met-AEA drops off the release of pro-inflammatory cytokines (IFN-γ, IL-17 and TNF-α) from inflamed mucosa of IBD patients [114], thus suggesting that activation of CB receptors may be useful for treatment of the disease; indeed, pharmacological elevation of eCB content attenuates colitis symptoms in wild-type mice, but not in CB^−/−₁ and CB^−/−₂ littermates [115]. Accordingly, activation of CB₂ receptor: (1) reduces the number of neutrophils, mast, CD4⁺, NK and T cells, in intestinal lamina propria and mesenteric lymph nodes of IL-10^−/− mice (which spontaneously develop chronic colitis at 12 weeks of age) [116]; (2) reduces the number of macrophages and IFNγ-expressing cells in dextran sodium sulphate-treated mice (which are affected by acute colitis) [117]. Conversely, we found that human inflamed IBD mucosa expressed more CB₁ than uninflamed mucosa without changes in CB₂ content [114]. Differences in species (humans versus mice), as well as in IBD experimental models, might underlie these discrepancies. Another interesting finding is that, in celiac disease, AEA seems to act as a pro-inflammatory compound: active celiac subjects show high levels of CB receptors, as well as of AEA (and PEA) in their mucosa (due to increased NAPE-PLD activity), which return to basal levels with a gluten-free diet [118–120].

eCB signalling appears to be also involved in immune responses associated to atherogenesis and its clinical manifestations, although its exact role is quite controversial. In atherosclerosis-prone apolipoprotein E-deficient (ApoE^−/−) mice, CB₂ stimulation reduces both infiltrating neutrophils and intraplaque MMP-9 levels, thus restraining plaque susceptibility to rupture [69]; coherently, leukocyte infiltration in atherosclerotic plaques increases in double knocked out mice for ApoE and CB₂ receptor or in irradiated ApoE^−/− mice reconstituted with CB^−/−₂ bone marrow [121]. On the contrary, Willecke and co-workers [122] reported that neither genetic deficiency nor activation of CB₂ receptor was able to modulate atherogenesis in low-density lipoprotein receptor knockout mice, while Lenglet’s group [123] showed that in ApoE^−/− mice feeding high-cholesterol diet, pharmacological and genetic ablation of FAAH enhanced neutrophil recruitment. Accordingly, FAAH deletion exacerbated myocardial injury by increasing myocardial neutrophil infiltration [124].

An interesting finding with pharmacological implications is that, in primary peritoneal and immortalized macrophages, oxidized low-density lipoproteins increase eCB tone; subsequent activation of CB receptor triggers cholesterol accumulation in macrophages, by up-modulating expression of CD36 receptor (responsible for cholesterol influx), and by down-modulating expression of ATP-binding cassette protein A1 (responsible for cholesterol efflux) [125]. Accordingly, patients with coronary artery disease show enhanced serum levels of eCBs (including AEA, 2-AG, PEA and OEA), which might increase the risk of atherosclerotic plaque rupture, via promotion of neutrophil recruitment and activity [126].

Systemic and local inflammation is also deeply connected to ischemic stroke [127–129]. Using different experimental models, it has been shown that CB₂ activation limits cerebral infarct size, via attenuation of chemokine signalling, inflammatory cell infiltration, oxidative/nitrosative stress and/or cell death [130]. Furthermore, treatment of transient focal ischemic mice with selective CB₂ receptor agonists, before and after reperfusion, both prevents and reduces leukocyte migration, thus improving infarct outcome and motor function [74, 131, 132]. In a mouse model of liver ischemia/reperfusion injury, JWH133 protects against damage, by decreasing inflammatory cell infiltration, tissue and serum TNFα, MIP-1a/CCL3 and MIP-2/CXCL2 levels, as well as ICAM-1 expression [133]. It has also been hypothesized that receptors other than CB₂ might represent promising therapeutic approaches for ischemia-induced inflammation, since CBD attenuates TNFα production in Kupffer cells (resident macrophages of the liver), along with ICAM-1 expression and leukocyte adhesion to human sinusoidal endothelium [134].

Blood eCB system as a mirror of neurological diseases

In recent years, an increasing number of experimental observations have indicated that peripheral blood cells might represent a novel, non-invasive diagnostic tool of several neurological disorders, as dysregulation of their activity often mirrors central dysfunctions (Table 3).

In particular, patients suffering from distinct neurological diseases show alterations of the eCB system in their lymphocytes or/and platelets [135]. This is the case of peripheral lymphocytes from Huntington’s disease patients that have a remarkable decrease of FAAH activity and increase of endogenous AEA levels compared to healthy subjects, with no changes in other elements of the eCB system [136]. Similarly, AEA (but not 2-AG) levels are higher in peripheral lymphocytes of relapsing multiple sclerosis (MS) patients; in this case, increased blood AEA content depends on increased synthesis by NAPE-PLD and reduced degradation by FAAH, and mirrors increased AEA levels found in the cerebrospinal fluid [137]. AEA levels are increased in active MS lesions [138], coherently CB₂ receptor, absent in inactive plaques, is expressed in macrophages showing recent phagocytic activity, as well as in perivascular T lymphocytes [139]. Accordingly, T and B cells from MS patients had significantly high CB₁ and CB₂ expression, respectively [140].

It has been recently proposed that AEA may limit immune response associated to MS and, thus, protect brain from neuroinflammation, by restoring cytokine balance in microglia, via a CB₂-dependent mechanism [141, 142]. This hypothesis is supported by the evidence that AEA (but not 2-AG) levels were significantly elevated in B, T and NK cells prior interferon therapy and returned to values comparable to healthy subjects following 1 year of treatment [140]. Incidentally, we have shown that AEA has distinct immunomodulatory effects on human myeloid and plasmacytoid dendritic cells from healthy and MS individuals. AEA modulates cytokine production and Th-1/Th-17 commitment in both healthy dendritic cells and MS myeloid dendritic cells, while it has no effect at all in MS plasmacytoid dendritic cells. Such a lack of effect depends on increased FAAH expression in MS plasmacytoid dendritic cells [55]. This finding, together with the evidence that the expression of FAAH was unchanged in MS B, T and NK cells [140] seems to speak in favour of a specific regulation of FAAH activity in distinct blood cells.

Additionally, lymphocytes from Parkinson’s disease patients, whose cerebrospinal fluid contains high AEA levels [143], have FAAH expression and activity significantly lower than that found in healthy controls, thus indicating that enzyme dysfunction might represent a compensatory mechanism, also occurring at striatal level, aimed at compensating central dopamine deficiency [135]. Peripheral blood mononuclear cells of subjects with late-onset Alzheimer disease (AD) show increased FAAH activity, as a result of epigenetic regulation, identifying FAAH as a new potential biomarker for AD in easily accessible peripheral cells [144].

Alterations in the eCB system of immune cells have also been observed in psychiatric disorders. Decreased AEA hydrolysis (but not synthesis) has been found in lymphocytes derived from patients affected by attention-deficit/hyperactivity disorder, the most commonly diagnosed neurodevelopmental disorder in childhood [145]. Serum levels of both AEA and 2-AG also increase and correlate with blood pressure in women diagnosed with depression [146]. The relevance of blood eCBs tone has recently been sustained by a double-blind, randomized clinical trial, where cannabidiol treatment was shown to increase serum AEA levels that were correlated with clinical improvement of schizophrenia symptoms [147]. Moreover, CB₂ gene expression appears to be significantly upregulated in peripheral blood mononuclear cells from autistic children [148], with a specific increase of NAPE-PLD/FAAH expression ratio in their macrophages [149].

Also platelet eCB system has been shown to be altered in patients with some neurological disorders. This is the case of patients with migraine, whose platelets show altered serotonin concentration, which correlates with chronification of headache [150]. Platelets from female (but not male) patients with migraine without aura have increased activity of both FAAH and EMT, with no difference in the expression of CB receptors [150]. Such an observation may explain the prevalence of migraine in women, as increased degradation of platelet AEA, and thus lower blood AEA content, may contribute to reduce pain threshold [150]. Instead, platelets from chronic migraine (CM) and medication-overuse headache (MOH) subjects show reduced EMT and FAAH levels, compared to either controls or episodic migraine group, without differences in gender [151]. We recently identified a relationship between altered platelet FAAH activity and reduction in facilitation of pain processing in MOH subjects; this could represent the consequence of a mechanism devoted to acutely reduce eCB degradation upon pain [152]. Finally, decreased plasma AEA and 2-AG levels (especially in females) have also been reported in CM and MOH patients [153]. Interestingly, alterations of the eCB tone seem to reflect those of serotonin, as a correlation between the levels of this neurotransmitter and 2-AG has been found, particularly in MOH patients [153], hence supporting validity of platelets as models for neuronal pathophysiology.

Therapeutic exploitation

The wide pharmacopoeia of CB receptor ligands (including agonists, antagonists and inverse agonists) has offered the incentive for developing meaningful therapeutic approaches in a plethora of pathologies affecting humans due to inflammatory, immunological and oncological disorders [108, 154–156].

The only therapeutically relevant CB receptor ligands currently in use are Δ⁹-tetra-hydrocannabinol (Δ⁹-THC), its synthetic forms and closely related compounds (154). Sativex is a vaporized delivery system for purified Δ⁹-THC that has obtained approval status for treatment of neuropathic pain and spasticity in multiple sclerosis; Dronabinol, a synthetic Δ⁹-THC, is usually employed for treatment of neuropathic pain in multiple sclerosis, anorexia in AIDS and nausea and vomiting in cancer chemotherapy; Nabilone, a derivatized synthetic Δ⁹-THC, has been approved in UK, Canada and Mexico for cancer patients [154]. Sanofi-Synthelabo has developed CB receptor antagonists to be used in the clinic: initially approved for therapeutic use, the CB₁ antagonist SR141716A (Rimonabant, Accomplia) has been withdrawn because of serious concerns to the safety [157].

The immunosuppressive potency of eCBs, together with their ability to negatively impact the release of pro-inflammatory mediators, has allowed testing the eCB-based drugs in inflammatory experimental models and even in some human diseases [158, 159]. For example, inhaled Δ⁹-THC can restrain airway or gastrointestinal inflammation, suggesting its clinical application for treatment of asthma, inflammatory Bowel and Crohn’s diseases. Despite the body of evidences from pre-clinical studies, successful randomized trials are very few and, till now, it is difficult to translate the basic data in therapeutic interventions, because of several factors, including chemically labile structures, poor bioavailability, severe side effects, and failure to arrest disease progression.

Several aspects may account for this gap between in vitro and in vivo experimental data and clinical translation. First, currently available receptor agonists are not totally specific, so that, at high doses, agonists of one receptor may activate the other type of receptor, especially when the levels of CB₁ and CB₂ expression are considerably different [108]. This should be taken into account, considering that in many immunocytes, CB₂ activation exerts suppressive effects, while CB₁ activation is mainly responsible for the pro-inflammatory action of eCBs [160]. Another cause is that eCBs may exert different effects depending on specific steps of the disease. For example, CB agonists appear to be effective at early stages, while losing their efficacy at later time points, as it is the case of sepsis immunopathogenesis [158]: during the early hyper-inflammatory response, modulation of CB2 receptor is helpful to dampen down the uncontrolled over-activation of the innate immune system, but in later stages of sepsis immune-suppression occurs and, therefore, modulation of the eCB system is needed to enhance the inflammatory response.

Finally, potential side effects of eCB therapeutics, including those affecting the neurological (mood alterations, depression, psychosis) and/or cardiovascular (hypotension, ischemia, stroke, inflammation) systems should also be considered [161–164]. Given their immunoactivity, profound phenotypic changes may indeed occur after continued eCB exposure; increases in TNFα, IFNγ and IL-2 levels have been found in Dronabinol-treated patients [165], and marijuana users have experienced decrease in NK cell numbers, reduction of IL-2 levels, and increase in pro-inflammatory cytokines IL-10 and TGF1 [166]. Therefore, it is conceivable that, in the long term, therapeutic eCBs may have immunological side effects, including increased susceptibility to infectious agents, dysregulated production of cytokines, and alterations in cell-mediated immunity. This should be considered when eCB-based drugs are thought for treating diseases (such as AIDS, anorexia, cancer, obesity) where immune responses are impaired, so that prolonged exposure to eCBs has the potential to worsen an already compromised immune system.

Conclusions and future perspectives

Since the discovery of the eCB system in the early 1990s, an ever-growing body of literature data has helped to better define its role in haematopoiesis and bone marrow function, as well as in platelet and leukocyte pathophysiology. Moreover, the evidence that the eCB system (and particularly CB₂ receptor) is dysregulated in several blood cancers and pathologies characterized by abnormal inflammatory responses, clearly supports that it should be considered a therapeutic target to prevent (and even treat) blood-related disorders. Nonetheless, the complexity of the eCB system requires special caution in drawing eCB therapeutic applications, as activation of these pathways may either represent a compensatory response to a specific insult (thus slowing progression of the disease) or may be pathogenic (thus exacerbating symptoms). A typical example of eCB system complexity is offered by platelets that may store eCBs, may be arachidonate reservoirs, or may release the oxygenated eCB derivatives to activate other cells; this multi-faced aspect requires being very careful in the therapeutic application of eCBs, to optimize benefits and minimize risks.

An interesting finding is that several elements of blood eCB system appear to follow the same alterations observed in some neurological disorders, thus leading to the challenging hypothesis that blood eCB system might be a central nervous system mirror, suitable for novel, non-invasive diagnostic strategies for brain diseases. Due to the complexity of neurological disorders, it is very difficult to have perfect and accessible biomarkers useful for measuring the progress of neurological disorders or the effects of treatment. Therefore, it is wished to better clarify the role of eCB system in these diseases to have effective therapeutic targets.

Abbreviations

2-AG

2-Arachidonoylglycerol

Met-AEA

2-methylarachidonyl-(2′-fluoroethyl)amide

ABHD

a/b-hydrolase

AML

Acute myeloid leukaemia

ApoE

Apolipoprotein E

CB

Cannabinoid

CM

Chronic migraine

eCB

Endocannabinoid

EMT

eCB membrane transporter

eNOS

Endothelial nitric oxide synthase

ERK

Extracellular signal-related kinase

FAAH

Fatty acid amide hydrolase

fMLP

Formyl-Met-Leu-Phe

G-CSF

Granulocyte-colony-stimulating factor

GM-CSF

Granulocyte-macrophage colony-stimulating factor

HETE-G

Hydroxyeicosatetraenoyl glycerylester

(S)-HAEA

Hydroxyeicosatetraenoylethanolamide

IBD

Inflammatory bowel disease

IFNγ

Interferon γ

IL

Interleukin

LTB4

Leukotriene B4

LPS

Lipopolysaccharide

MCP-1

Macrophage-chemotactic protein 1

MMP-9

Matrix metalloprotease-9

MOH

Medication-overuse headache

MAGL

Monoacylglyceride lipase

MS

Multiple sclerosis

NAPE-PLD

N-acylphosphatydiletanolamine phospholipase D

anandamide, AEA

N-arachidonoylethanolamine

NK

Natural killer

NO

Nitric oxide

PEA

N-palmitoylethanolamine

OEA

N-oleoylethanolamine

PPARs

Peroxisome proliferator-activated receptors

PI3 K

Phosphoinositide 3kinase

PGE₂

Prostaglandin E2

Th

T helper

TRPV1

Transient receptor potential vanilloid 1

TNFα

Tumour necrosis factor α

CB₁

Type-1 cannabinoid receptor

CB₂

Type-2 cannabinoid receptor