基因敲除
SMAD公司
C2C12型
竞争性内源性RNA
细胞生物学
骨骼肌
纤维化
小RNA
心肌细胞
癌症研究
分子生物学
体内
转化生长因子
生物
长非编码RNA
转染
化学
细胞生长
CTGF公司
基因沉默
下调和上调
小干扰RNA
信使核糖核酸
核糖核酸
RNA干扰
小发夹RNA
医学
内分泌学
内科学
肌发生
基因
生物化学
遗传学
作者
Jiwu Chen,Zhiwen Luo,Shaohua Liu,Qingyan Chen,Siyang Liu
标识
DOI:10.1111/1440-1681.13489
摘要
Emerging evidence has indicated long non-coding RNAs (lncRNAs) play important roles in diverse biological processes, including fibrosis. Here, we report that lncRNA H19 is able to promote skeletal muscle fibrosis. lnc-H19 was identified to be highly expressed in skeletal muscle fibrosis in vivo and in vitro; while lnc-H19 knockdown attenuated fibrosis in vitro. The knockdown of lnc-H19 was proved to inhibit the activation of the TGFβ/Smad pathway in C2C12 myoblasts by sponging miR-20a-5p to regulate Tgfbr2 expression through the competing endogenous RNA function. Our study elucidates the roles of the lnc-H19-miR-20a-5p-Tgfbr2 axis in regulating the TGFβ/Smad pathway of myoblast fibrogenesis, which might provide a promising therapeutic target for skeletal muscle fibrosis.
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