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. 2019 Aug 13;20(16):3938. doi: 10.3390/ijms20163938

Table 5.

Studies dealing with other conditions (ACE2: Angiotensin Converting Enzyme 2; BMDM: bone marrow-derived macrophages; BSM: bronchial smooth muscle; CF: Cystic Fibrosis; CIV: canine influenza virus; hBSMCs: human BSM cells; HLMECs: human lung microvascular endothelial cells; HPASMCs: human pulmonary arterial smooth muscle cells; HS: honeysuckle; HUVECs: human umbilical vein endothelial cells; Igfbp5: insulin-like growth factor binding protein 5; MDCK: Madin-Darby Canine Kidney; MDM: monocyte-derived macrophages; MSC: mesenchymal stromal cell; PASMC: pulmonary arterial smooth muscle cells; PBMC: peripheral blood mononuclear cells; SARS-CoV: severe acute respiratory syndrome coronavirus).

Other Conditions
Humans
Study Disease Sample miRNAs Findings
Chatterjee et al. (2014) [41] Lung cell dysfunction HLMECs, HUVECs miR-147b MiR-147b antagomir increased total and cell surface expression of ADAM15 in endothelial cells (p < 0.05)
Ge et al. (2016) [82] Lung fibrosis Humans: bronchial epithelia from lung transplant patients. Cells: primary fibroblasts isolated from human lungs miR-323a-3p Antagomirs for miR-323a-3p augment murine lung fibrosis after bleomycin injury (p < 0.05)
Sharma et al. (2018) [58] HIV infection and substance abuse Human monocyte derived macrophages, HPASMCs miR-130a Transfection of HPASMCs with antagomir-130a–ameliorated the extracellular vesicles-induced effect (p < 0.001)
Yuan et al. (2018) [69] Tuberculosis Fifty patients, 20 controls. Monocytes isolated from peripheral blood mononuclear cells miR-196b-5p antagomir-196b-5p promoted Bacillus Calmette–Guérin uptake in MDMs or differentiated U937 cells (p < 0.05)
Animals
Study Disease Sample miRNAs Findings
Krützfeldt et al. (2005) [7] Various conditions Mice models miR-16, miR-122, miR-192, miR-194 Intravenous administration of antagomirs reduced miRNA levels in liver, lung, kidney, heart, intestine, fat, skin, bone marrow, muscle, ovaries, and adrenals
Chiba et al. (2009) [83] Abnormal BSM contraction BSM cells, bronchial tissues of BALB/c mice miR-133a Up-regulation of RhoA when endogenous miR-133a function inhibited by its antagomir in hBSMCs (p < 0.05). No effect (p > 0.05) of miR-133b and let-7a antagomirs
Pandit et al. (2010) [84] Pulmonary Fibrosis Animals: mice models.
Cells: 10 Idiopathic Pulmonary Fibrosis, 10 control tissues
Let-7d Let-7d antagomir decreased expression of CDH1 and TJP1 and increased COL1A1 and HMGA2 expression in the lungs (p < 0.05)
Rosenberger et al. (2012) [56] Influenza C57Bl/6, MyD88null mice miR-451 Three types of primary dendritic cells treated with antagomirs against miR-451 secreted elevated levels of IL-6 (p< 0.01), TNF (p < 0.05), CCL5/RANTES (p < 0.05), and CCL3/MIP1α (p < 0.01)
Asquith et al. (2014) [85] Chronic ethanol consumption From non-human primates: PBMC, mesenteric and tracheobronchial lymph nodes, jejunum, duodenum, ileum, and descending colon miR-181a, miR-221 (in PBMC), miR-155 (in colon) Transfection of miRNA antagomirs upregulated both STAT-3 (p < 0.05)/ARNT (p < 0.001), VEGF (p < 0.05)/HGF (p < 0.01)/G-CSF (p < 0.05)
Zhang et al. (2015) [52] Various disorders Animals: BALB/c mice.
Cells: 4T1 murine breast cancer cells
miR-10b Antagomir-10b and PTX delivered by D-Lip delays the growth of 4T1 tumors and reduce lung metastases; Hoxd10 expression in tumors up-regulated (p < 0.01)
Zhou et al. (2015) [54] Influenza Animals: six groups of mice (five mice per group), including control group.
Cells: MDCK cells
miR-2911 Inhibitory effect of HS decoction on viral replication abolished by anti-miR2911 (p < 0.05)
Podsiad et al. (2015) [31] Pneumonia Animals: wild-type C57BL/6 mice.
Cells: Human lung macrophages
miR-155 miR-155 antagomir improved lung bacterial clearance by 4.2-fold
Zhou et al. (2016) [86] Systemic Lupus Erythematosus Animals: C57BL/6J (B6) and B6.Cg-Mir155tm1.1Rsky/J mice.
Cells: Hepa 1-6 cells
miR-155 Disease progression reduced by 20% by in vivo using of antimiR-155
Ma et al. (2017) [71] Hypoxia Animals: adult male Wistar rats.
Cells: PASMC cultured
miR-125a miR-125a antagomir mimicked the hypoxic damage effects to mitochondrial homeostasis (p < 0.05)
Morales et al. (2017) [87] SARS-CoV Animals: female mice.
Cells: mouse delayed brain tumor cells expressing the murine SARS-CoV receptor ACE2
svRNA-nsp3.1, svRNA-nsp3.2, svRNA-N, miR-877 Antagomirs reduced partially (svRNA-nsp3.1), or totally (svRNA-nsp3.2, svRNA-N, miR-877), the luciferase activity
Zhou et al. (2017) [88] Influenza Animals: beagles.
Cells: MDCK cells
cfa-miR-143 Anti-cfa-miR-143 caused upregulation of Igfbp5 in CIV-infected MDCK cells
Fehl et al. (2019) [44] Bronchopulmonary dysplasia Newborn C57BL/6J mice N/A AntagomiRs impacted lung volume (p < 0.05), septal thickness (p < 0.01), and the transcriptome (p < 0.05) of developing mouse lungs
Li et al. (2019) [28] Lung ischemia Mail C57/BL6 mice miR-21-5p Pre-treatment of MSCs with miR-21-5p antagomir decreased miR-21-5p expression level in exosomes secreted
Tamgue et al. (2019) [89] Tuberculosis Bone marrow-derived macrophages generated from male BALB/c mice miR-143, miR-365 Antagomirs for miR-143 and miR-365 decreased the intracellular growth of Mtb HN878, reduced the production of IL-6 (p < 0.001) and CCL5 (p < 0.01 for miR-143, p < 0.05 for miR-365) and promoted the apoptotic death of Mtb HN878-infected BMDMs (p < 0.01 for miR-143, p < 0.05 for miR-365)
Zhang et al. (2019) [90] Influenza Animals: C57BL/6 mice.
Cells: human pulmonary epithelial cell line A549
miR-146a Downregulation of miR-146a inhibits Influenza A Virus replication by enhancing type I IFN response through TRAF6 in vitro and in vivo (p < 0.01)
Cell Lines
Study Disease Sample miRNAs Findings
Chiba et al. (2009) [83] Abnormal BSM contraction BSM cells, bronchial tissues of BALB/c mice miR-133a Up-regulation of RhoA when endogenous miR-133a function inhibited by its antagomir in hBSMCs (p < 0.05). No effect (p > 0.05) of miR-133b and let-7a antagomirs
Pandit et al. (2010) [84] Pulmonary Fibrosis Animals: mice models.
Cells: 10 Idiopathic Pulmonary Fibrosis and 10 control tissues
Let-7d Let-7d antagomir decreased expression of CDH1 and TJP1, and increased COL1A1 and HMGA2 expression in the lungs (p < 0.05)
Bhattacharyya et al. (2011) [29] Cystic Fibrosis Lung epithelial cells miR-155 Antagomir-155 in CF cells down-regulates miR-155 expression by 85%; IL-8 mRNA levels decreased of 70% and IL-8 protein levels by 11-fold
Chatterjee et al. (2014) [41] Lung cell dysfunction HLMECs, HUVECs miR-147b MiR-147b antagomir increased total and cell surface expression of ADAM15 in endothelial cells (p < 0.05)
Fabbri et al. (2014) [43] Cystic Fibrosis CF bronchial epithelial IB3-1 cells infected by Pseudomonas aeruginosa miR-93 IL-8 up-regulation in uninfected cells treated with antagomiR-93 (p < 0.01)
Zhang et al. (2015) [52] Various disorders Animals: BALB/c mice.
Cells: 4T1 murine breast cancer cells
miR-10b Antagomir-10b and PTX delivered by D-Lip delays the growth of 4T1 tumors and reduce the lung metastases; up-regulated Hoxd10 in tumors (p < 0.01)
Zhou et al. (2015) [54] Influenza Animals: six groups of mice (five mice per group), including control group.
Cells: MDCK cells
miR-2911 Inhibitory effect of HS decoction on viral replication abolished by anti-miR2911 (p < 0.05)
Ge et al. (2016) [82] Lung fibrosis Humans: bronchial epithelia from lung transplant patients. Cells: primary fibroblasts from human lung explants miR-323a-3p Antagomirs for miR-323a-3p augment murine lung fibrosis after bleomycin injury (p < 0.05)
Podsiad et al. (2015) [31] Pneumonia Animals: wild-type C57BL/6 mice.
Cells: human lung macrophages
miR-155 AntimiR-155 improved lung bacterial clearance by 4.2-fold compared with controls
Zhou et al. (2016) [86] Systemic Lupus Erythematosus Animals: C57BL/6J (B6) and B6.Cg-Mir155tm1.1Rsky/J mice.
Cells: Hepa 1-6 cells
miR-155 Disease progression, reduced by 20% by in vivo silencing of miR-155 using antimiR-155
Bartoszewska et al. (2017) [36] Hypoxia Hypoxia-induced human airway epithelial cell lines Calu-3 and 16HBE14o-; normal primary bronchial epithelial cells miR-200b Manipulation of miRNA levels during normoxia and hypoxia by antagomirs increased CFTR mRNA levels (p < 0.05)
Ma et al. (2017) [71] Hypoxia Animals: adult male Wistar rats.
Cells: PASMC cultured
miR-125a miR-125a antagomir mimicked the hypoxic damage effects to mitochondrial homeostasis (p < 0.05)
Morales et al. (2017) [87] SARS-CoV Animals: Female mice.
Cells: mouse delayed brain tumor cells expressing the murine SARS-CoV receptor ACE2
svRNA-nsp3.1, svRNA-nsp3.2, svRNA-N, miR-877 Antagomirs reduced partially (svRNA-nsp3.1), or totally (svRNA-nsp3.2, svRNA-N, miR-877), the luciferase activity
Shentu et al. (2017) [26] Lung fibrosis Human bone marrow-derived Mesenchymal Stem Cells miR-199a/b-3p, 21-5p, 630, 22-3p, 196a-5p, 199b-5p, 34a-5p, and 148a-3p AntagomiR-630 abrogated the effect of extracellular vesicles on CDH2 expression (p < 0.05)
Zhou et al. (2017) [88] Influenza Animals: beagles.
Cells: MDCK cells
cfa-miR-143 Anti-cfa-miR-143 caused upregulation of Igfbp5 in CIV-infected MDCK cells
Sharma et al. (2018) [58] HIV infection and substance abuse Human monocyte derived macrophages, HPASMCs miR-130a Transfection of HPASMCs with antagomir-130a ameliorated the extracellular vesicles-induced effect (p < 0.001)
Yuan et al. (2018) [69] Tuberculosis Fifty patients, 20 controls. Monocytes isolated from peripheral blood mononuclear cells miR-196b-5p Antagomir-196b-5p promoted Bacillus Calmette–Guérin uptake in MDMs or differentiated U937 cells (p < 0.05)
Tamgue et al. (2019) [89] Tuberculosis Bone marrow-derived macrophages generated from male BALB/c mice miR-143, miR-365 Antagomirs for miR-143 and miR-365 decreased the intracellular growth of Mtb HN878, reduced the production of IL-6 (p < 0.001) and CCL5 (p < 0.01 for miR-143, p < 0.05 for miR-365), and promoted the apoptotic death of Mtb HN878-infected BMDMs (p < 0.01 for miR-143, p < 0.05 for miR-365)
Zhang et al. (2019) [90] Influenza Animals: C57BL/6 mice.
Cells: human pulmonary epithelial cell line A549
miR-146a Downregulation of miR-146a inhibits Influenza A Virus replication by enhancing type I IFN response through TRAF6 in vitro and in vivo (p < 0.01)