Hsa_circ_0012919 regulates expression of MDA5 by miR-125a-3p in CD4+ T cells of systemic lupus erythematous

Author:

Zhang Chengzhong12,Zhang Chao32,Ji Jie1,Xiong Xixi1,Lu Yan1ORCID

Affiliation:

1. Department of Dermatology, Jiangsu Province Hospital, the First affiliated Hospital with Nanjing Medical University, China

2. *These authors contributed equally to this work.

3. Department of Dermatology, Institute of Fudan-Minhang Academic Health System, Minhang Hospital, Fudan University, China

Abstract

Systemic lupus erythematous (SLE) is an autoimmune disease with production of various autoantibodies directed against various autoantigens. But the research on melanoma differentiation-associated gene 5 (MDA5) in SLE is still scarce. Here we try to elucidate the effect of hsa_circ_0012919 on MDA5 and its potential clinical value in SLE. CD4+ T cells from SLE patients and healthy control subjects were isolated. Expression of hsa_circ_0012919 and MDA5, and methylation level of MDA5 promoter were detected. Then expression and methylation level of MDA5 promoter was examined after transfection of hsa_circ_0012919-targeted siRNA and plasmids. Expression of hsa_circ_0012919 and MDA5 were further confirmed to be significantly higher in CD4+ T cells of SLE patients ( p < 0.05), methylation level of MDA5 promoter was significantly lower in CD4+ T cells of SLE patients ( p < 0.05), and expression of MDA5 mRNA was correlated with SLE parameters ( p < 0.05). Downregulation or overexpression of hsa_circ_0012919 regulated (1) the expression of MDA5 in a dose-dependent manner and (2) the DNA methylation of MDA5 promoter in CD4+ T cells of SLE. Finally, hsa_circ_0012919 could regulate MDA5 by miR-125a-3p. Hsa_circ_0012919 regulated the expression and methylation of MDA5 in the CD4+ T cells of SLE patients, and hsa_circ_0012919 could regulate MDA5 by miR-125a-3p.

Publisher

SAGE Publications

Subject

Rheumatology

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