Up-regulated miR-145 Expression Inhibits Porcine Preadipocytes Differentiation by Targeting IRS1

被引:64
作者
Guo, Yunxue [1 ]
Chen, Yaosheng [1 ,2 ]
Zhang, Yun [1 ]
Zhang, Yue [1 ]
Chen, Luxi [1 ]
Mo, Delin [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Life Sci, State Key Lab Biocontrol, Guangzhou 510006, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Guangdong Prov Engn & Technol R&D Ctr Pig Breedin, Guangzhou 510006, Guangdong, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
miR-145; IRS1; inhibit; dedifferentiated fat cells; adipogenesis; INSULIN-RECEPTOR SUBSTRATE-1; ADIPOSE-TISSUE; ADIPOGENIC DIFFERENTIATION; ADIPOCYTE DIFFERENTIATION; CELL-LINES; GROWTH; MICRORNA-143;
D O I
10.7150/ijbs.4597
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Generally, most miRNAs that were up-regulated during differentiation promoted adipogenesis, but our research indicated that up-regulation of miR-145 in porcine preadipocytes did not promote but inhibit adipogenesis. In this study, miR-145 was significantly up-regulated during porcine dedifferentiated fat (DFAT) cells differentiation. In miR-145 overexpressed DFAT cells, adipogenesis was inhibited and triglycerides accumulation was decreased after hormone stimulation (P<0.05). Furthermore, up-regulation of miR-145 expression repressed induction of mRNA levels of adipogenic markers, such as CCAAT/enhancer-binding protein a (C/EBP alpha), and peroxisome proliferator-activated receptor gamma 2 (PPAR gamma 2). These effects caused by miR-145 overexpression were mediated by Insulin receptor substrate 1 (IRS1) as a mechanism. These data suggested that induced miR-145 expression during differentiation could inhibit adipogenesis by targeting IRS1, and miR-145 may be novel agent for adipose tissue engineering.
引用
收藏
页码:1408 / 1417
页数:10
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