Xie Junfeng, Cheng Na, Huang Zhanchao, Shu Xu, Xiang Tianxin
Department of Hospital Infection Control, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330000, P.R. China.
Department of Gastroenterology, The People's Hospital of Ganzhou City, Ganzhou, Jiangxi 341000, P.R. China.
Exp Ther Med. 2022 Jun 27;24(2):537. doi: 10.3892/etm.2022.11474. eCollection 2022 Aug.
The present study aimed to explore the biological functions of microRNA (miR)-146b-5p and homeodomain interacting protein kinase 1 (HIPK1) in the progression of hepatic fibrosis (HF) and to identify the underlying mechanism. A rat HF model was established by administering a subcutaneous injection of carbon tetrachloride (CCl). Relative levels of miR-146b-5p and HIPK1 in fibrotic rat liver tissues and the rat hepatic stellate cell (HSC) line HSC-T6 were measured by quantitative reverse transcription PCR, western blotting and immunohistochemistry. Following activation of HSC-T6 cells by lipopolysaccharide (LPS) induction, cell viability was examined by MTT assay. Transfection of miR-146b-5p mimic or inhibitor into HSC-T6 cells was performed, with the aim to identify the influence of miR-146b-5p on HSC-T6 cell behavior. The targeting relationship between miR-146b-5p and HIPK1 was predicted by TargetScan 7.2 and StarBase 3.0 and it was later verified by a dual-luciferase reporter assay. Through lentivirus transfection, the biological function of HIPK1 in regulating the progression of HF and the underlying mechanism were investigated. The results showed that miR-146b-5p was upregulated in liver tissues of rats with HF and activated HSC-T6 cells, while HIPK1 was downregulated in liver tissues of rats with HF and activated HSC-T6 cells. miR-146b-5p was able to upregulate the activation markers of LPS-induced HSC-T6 cells, upregulate COL1A1 and TGF-β, increase cell viability and contribute to fibrosis progression. HIPK1 was validated as the direct target of miR-146b-5p and its overexpression could effectively reduce the effect of miR-146b-5p in contribution to the progression of HF. In conclusion, miR-146b-5p was significantly upregulated during the progression of HF. By targeting and downregulating HIPK1, miR-146b-5p could significantly activate HSCs, upregulate COL1A1 and TGF-β and contribute to fibrosis progression. miR-146b-5p is a potential biomarker and therapeutic target for HF.
本研究旨在探讨微小RNA(miR)-146b-5p和同源结构域相互作用蛋白激酶1(HIPK1)在肝纤维化(HF)进展中的生物学功能,并确定其潜在机制。通过皮下注射四氯化碳(CCl)建立大鼠HF模型。采用定量逆转录聚合酶链反应、蛋白质免疫印迹法和免疫组织化学法检测纤维化大鼠肝组织及大鼠肝星状细胞(HSC)系HSC-T6中miR-146b-5p和HIPK1的相对水平。在用脂多糖(LPS)诱导激活HSC-T6细胞后,通过MTT法检测细胞活力。将miR-146b-5p模拟物或抑制剂转染到HSC-T6细胞中,以确定miR-146b-5p对HSC-T6细胞行为的影响。通过TargetScan 7.2和StarBase 3.0预测miR-146b-5p与HIPK1之间的靶向关系,随后通过双荧光素酶报告基因实验进行验证。通过慢病毒转染,研究HIPK1在调节HF进展中的生物学功能及其潜在机制。结果显示,在HF大鼠肝组织和激活的HSC-T6细胞中,miR-146b-5p上调,而HIPK1下调。miR-146b-5p能够上调LPS诱导的HSC-T6细胞的激活标志物,上调COL1A1和转化生长因子-β(TGF-β),增加细胞活力,并促进纤维化进展。HIPK1被证实为miR-146b-5p的直接靶点,其过表达可有效降低miR-146b-5p对HF进展的促进作用。总之,在HF进展过程中,miR-146b-5p显著上调。通过靶向并下调HIPK1,miR-146b-5p可显著激活HSCs,上调COL1A1和TGF-β,并促进纤维化进展。miR-146b-5p是HF的潜在生物标志物和治疗靶点。