Wu Jing, Li Jiang, Chen Wei-Kang, Liu Shang, Liu Jian-He, Zhang Jing-Song, Fang Ke-Wei
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Kunming Medical University, Kunming, China.
Department of Urology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Cell Physiol Biochem. 2017;42(5):1870-1887. doi: 10.1159/000479570. Epub 2017 Aug 3.
BACKGROUND/AIMS: This study investigated whether microRNA-214 (miR-214) targets mitofusin-2 (Mfn2) in the process of fibroblast differentiation of adipose-derived mesenchymal stem cells (ADMSCs) during pelvic floor dysfunction (PFD) in Sprague Dawley (SD) rats with birth trauma.
The ADMSCs were isolated from 4-6 week male SD rats (n = 20) and were cultured and divided into the blank, miR-214 mimic negative control (NC), miR-214 mimic, miR-214 inhibitor NC, miR-214 inhibitor, empty vector, Mfn2 over-expression and miR-214 + Mfn2 over-expression groups. Fibroblast differentiation of ADMSCs was measured with immunocytochemistry and immunofluorescence methods. The expression of miR-214 and the mRNA and protein expression of Mfn2, FSP1, Collagen I, Collagen III, Elastin, LOX, Fibulin-5, PPAR-γ and Runx2 were detected using quantitative real-time polymerase chain reaction (qRT-PCR) and Western blotting, respectively. A dual-luciferase reporter assay was performed to confirm whether Mfn2 was the target gene of miR-214.
During ADMSC differentiation into fibroblasts, miR-214 expression was up-regulated, but the expression of Mfn2 was down-regulated. Fibroblast differentiation of ADMSCs was promoted in the miR-214 mimic group but was inhibited in the miR-214 inhibitor and Mfn2 over-expression groups. The expression of Mfn2 was decreased, but the expression of FSP1, Collagen I, Collagen III, Elastin, LOX, Fibulin-5, PPAR-γ or Runx2 was increased in the miR-214 mimic group; the miR-214 inhibitor group and Mfn2 over-expression group exhibited the opposite results. Mfn2 was the target gene of miR-214.
The study provided strong evidence that miR-214 could promote fibroblast differentiation of ADMSCs by down-regulating Mfn2 to improve PFD in SD rats with birth trauma.
背景/目的:本研究调查了在出生创伤的Sprague Dawley(SD)大鼠盆底功能障碍(PFD)过程中,微小RNA-214(miR-214)在脂肪来源间充质干细胞(ADMSCs)成纤维细胞分化过程中是否靶向丝裂原活化蛋白激酶2(Mfn2)。
从4-6周龄雄性SD大鼠(n = 20)中分离ADMSCs,进行培养并分为空白组、miR-214模拟物阴性对照组(NC)、miR-214模拟物组、miR-214抑制剂NC组、miR-214抑制剂组、空载体组、Mfn2过表达组和miR-214 + Mfn2过表达组。采用免疫细胞化学和免疫荧光方法检测ADMSCs的成纤维细胞分化情况。分别使用定量实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹法检测miR-214的表达以及Mfn2、FSP1、胶原蛋白I、胶原蛋白III、弹性蛋白、赖氨氧化酶(LOX)、纤连蛋白-5、过氧化物酶体增殖物激活受体γ(PPAR-γ)和 runt相关转录因子2(Runx2)的mRNA和蛋白表达。进行双荧光素酶报告基因检测以确认Mfn2是否为miR-214的靶基因。
在ADMSCs向成纤维细胞分化过程中,miR-214表达上调,但Mfn2表达下调。miR-214模拟物组促进了ADMSCs的成纤维细胞分化,而miR-214抑制剂组和Mfn2过表达组则抑制了该分化。miR-214模拟物组中Mfn2表达降低,但FSP1、胶原蛋白I、胶原蛋白III、弹性蛋白、LOX、纤连蛋白-5、PPAR-γ或Runx2表达增加;miR-214抑制剂组和Mfn2过表达组呈现相反结果。Mfn2是miR-214的靶基因。
该研究提供了有力证据,表明miR-214可通过下调Mfn2促进ADMSCs的成纤维细胞分化,从而改善出生创伤SD大鼠的PFD。