Mechanism of miR-381 on macrophage infiltration in polymyositis by targeting stromal cell derived actor-1

CHEN Zhao-ying HONG Wen-ke

Acta Anatomica Sinica ›› 2022, Vol. 53 ›› Issue (2) : 183-189.

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Acta Anatomica Sinica ›› 2022, Vol. 53 ›› Issue (2) : 183-189. DOI: 10.16098/j.issn.0529-1356.2022.02.007
Cell and Molecules Biology

Mechanism of miR-381 on macrophage infiltration in polymyositis by targeting stromal cell derived actor-1

  • CHEN Zhao-ying  HONG Wen-ke*
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Abstract

Objective To explore the mechanism of miR-381 on the infiltration of polymyositis (PM) macrophages by targeting stromal cell derived factor-1 (SDF-1).   Methods PM model mouse was constructed by rabbit myosin (1.5 mg), mycobacterium tuberculosis (5 mg) and pertussis toxin (500 ng). The 30 PM model mice were divided into control group and PM+miR-381 group (n=15/group). During the same period, 15 healthy mice were used as a control group. Mice in the PM+miR-381 group were injected with miR-381 agomir (300 μg) intraperitoneally for 2 weeks. Serum creatine kinase (s-CK), interleukin (IL)-1β and IL-6 levels in serum of each group of mice, and the pathological changes of muscle tissue were detected and compared. The macrophage marker protein F4/80 was detected by immunohistochemical staining to assess the infiltration of macrophages. The expression levels of miR-381 and SDF-1 mRNA and protein in muscle tissues of each group were detected. The target relationship between miR-381 and SDF-1 was verified by dual luciferase report. Mouse macrophages were divided into miR-381 NC group and miR-381 mimic group. The SDF-1 mRNA and protein levels in each group were detected by Real-time PCR and Western blotting. Transwell was used to detect the level of cell migration to evaluate the infiltration capacity.   Results The above indicators of the three groups were significantly different (P<0.05). The level of miR-381 in the muscle tissue of the PM group was significantly lower than that of the control group, s-CK, IL-1β, IL-6, histological score, macrophage infiltration, and SDF-1 mRNA and protein expression levels were significantly higher than those of the control group (P<0.05). The level of miR-381 in the muscle tissue of the PM+miR-381 group was significantly higher than that of the PM group, s-CK, IL-1β, IL-6, histological score, macrophage infiltration, and SDF-1 mRNA and protein expression levels were significantly lower than those in the PM group (P<0.05). The dual luciferase report result  indicated that miR-381 could target binding to SDF-1. The expression levels of SDF-1 mRNA and protein in macrophages in the miR-381 mimic group were significantly lower than those in the miR-381 NC group (P<0.05). The number of migrating cells in the miR-381 mimic group was significantly lower than that in the miR-381 NC group (P<0.05).   Conclusion Increasing the level of miR-381 can inhibit the inflammatory infiltration ability of macrophages by targeting the expression of SDF-1, thereby alleviating PM.

Key words

Polymyositis / Stromal cell derived factor-1 / Macrophage infiltration / Immunohistochemistry / Dual luciferase report / Mouse

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CHEN Zhao-ying HONG Wen-ke. Mechanism of miR-381 on macrophage infiltration in polymyositis by targeting stromal cell derived actor-1[J]. Acta Anatomica Sinica. 2022, 53(2): 183-189 https://doi.org/10.16098/j.issn.0529-1356.2022.02.007

References

[1] Sasaki H, Kohsaka H. Current diagnosis and treatment of polymyositis and dermatomyositis [J]. Mod Rheumatol, 2018, 28(6): 913-921.
[2] Yan W, Chen C, Chen H. Estrogen downregulates miR-21 expression and induces inflammatory infiltration of macrophages in polymyositis: role of CXCL10 [J]. Mol Neurobiol, 2017, 54(3): 1631-1641.
[3] Yu L, Yu L, Pham Q, et al. Transcriptional and translational-uncoupling in regulation of the CXCL12 and its receptors CXCR4, 7 in THP-1 monocytes and macrophages[J]. Immun Inflamm Dis,2018,6(1):106-116.
[4] Kuang L, Wu J, Su N, et al. FGFR3 deficiency enhances CXCL12-dependent chemotaxis of macrophages via upregulating CXCR7 and aggravates joint destruction in mice[J]. Ann Rheum Dis, 2020, 79(1): 112-122.
[5] Zhu J, Liu B, Wang Z, et al. Exosomes from nicotine-stimulated macrophages accelerate atherosclerosis through miR-21-3p/PTEN-mediated VSMC migration and proliferation [J]. Theranostics,2019, 9(23): 6901-6919.
[6] Liu WH, Yu X, Ren Y, et al. MicroRNA-140-5p promotes the proliferation of renal cancer cells through protein kinase C subtype ε [J]. Acta Anatomy Sinica, 2019, 50(2):185-191. (in Chinese)
刘伟红, 余肖, 任雨, 等. MicroRNA-140-5p通过蛋白激酶C亚型ε促进肾癌细胞增殖[J]. 解剖学报, 2019, 50(2):185-191.
[7] Song K, Li L, Sun G, et al. MicroRNA-381 regulates the occurrence and immune responses of coronary atherosclerosis via cyclooxygenase-2[J]. Exp Ther Med, 2018, 15(5): 4557-4563.
[8] Lim HX, Jung HJ, Lee A, et al. Lysyl-transfer RNA synthetase induces the maturation of dendritic cells through MAPK and NF-κB pathways, strongly contributing to enhanced Th1 cell responses[J]. J Immunol, 2018, 201(9): 2832-2841.
[9] Lee JS, Kwak G, Kim HJ, et al. miR-381 attenuates peripheral neuropathic phenotype caused by overexpression of PMP22 [J]. Exp Neurobiol, 2019, 28(2): 279-288.
[10] Motomura K, Yamashita H, Yamada S, et al. Clinical characteristics and prognosis of polymyositis and dermatomyositis associated with malignancy: a 25-year retrospective study [J]. Rheumatol Int, 2019, 39(10): 1733-1739.
[11] Sugiyama Y, Yoshimi R, Takeno M, et al. miR-1 is a novel biomarker for polymyositis/dermatomyositis-associated interstitial lung disease [J]. Mod Rheumatol, 2020, 30(5): 878-883.
[12] Jiang T, Huang Y, Liu H, et al. Reduced miR-146a promotes REG3A expression and macrophage migration in polymyositis and dermatomyositis [J]. Front Immunol, 2020, 11(1): 37-41.
[13] Lin CC, Law BF, Hettick JM. Acute 4, 4’-methylene diphenyl diisocyanate exposure-mediated downregulation of miR-206-3p and miR-381-3p activates inducible nitric oxide synthase transcription by targeting calcineurin/NFAT signaling in macrophages[J]. Toxicol Sci, 2020, 173(1): 100-113.
[14] Liu Y, Gao Y, Yang J, et al. MicroRNA-381 reduces inflammation and infiltration of macrophages in polymyositis via downregulating HMGB1 [J]. Int J Oncol, 2018, 53(3):1332-1342.
[15] Citro A, Pellegrini S, Dugnani E, et al. CCL2/MCP-1 and CXCL12/SDF-1 blockade by L-aptamers improve pancreatic islet engraftment and survival in mouse [J]. Am J Transplant, 2019, 19(11): 3131-3138.
[16] Zeng Y, Li B, Liang Y, et al. Dual blockade of CXCL12-CXCR4 and PD-1-PD-L1 pathways prolongs survival of ovarian tumor-bearing mice by prevention of immunosuppression in the tumor microenvironment [J]. FASEB J, 2019, 33(5): 6596-6608.
[17] Tian Y, Matsui S, Touma M, et al. MicroRNA-342 inhibits tumor growth via targeting chemokine CXCL12 involved in macrophages recruitment/activation[J]. Genes Cells, 2018, 23(12): 1009-1022.
[18] Piao JM, Wu W, Yang ZX, et al. MicroRNA-381 favors repair of nerve injury through regulation of the SDF-1/CXCR4 signaling pathway via LRRC4 in acute cerebral ischemia after cerebral lymphatic blockage[J]. Cell Physiol Biochem, 2018, 46(3): 890-906.
[19] Zheng GH, Wen X, Wang YJ, et al. MicroRNA-381-induced down-regulation of CXCR4 promotes the proliferation of renal tubular epithelial cells in rat models of renal ischemia reperfusion injury [J]. J Cell Biochem, 2018, 119(4): 3149-3161.
[20] Fang Z, Zhong M, Wang Y, et al. miR-381 and miR-489 suppress cell proliferation and invasion by targeting CUL4B via the Wnt/β-catenin pathway in gastric cancer [J]. Int J Oncol, 2019, 54(2): 733-743.
[21] Zhu XS, Zhou HY, Yang F, et al. miR-381-3p inhibits high glucose-induced vascular smooth muscle cell proliferation and migration by targeting HMGB1 [J]. J Gene Med, 2020, 9(9): e3274-e-3278.
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