Lv Shun, Ma Meilin, Sun Yunmei, Wang Xiangming, Qimuge Naren, Qin Jin, Pang Weijun
Laboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi Province, People's Republic of China.
Anim Cells Syst (Seoul). 2017 Jun 15;21(4):269-277. doi: 10.1080/19768354.2017.1337046. eCollection 2017.
MicroRNAs have been regarded to play a crucial role in the proliferation of different cell types including preadipocytes. In our study, we observed that miR-129-5p was down-regulated during 3T3-L1 preadipocyte proliferation, while the expression of G3BP1 showed a contrary tendency. 5-Ethynyl-2'-deoxyuridine (EdU) incorporation assay and flow cytometry showed that overexpression of miR-129-5p could bring about a reduction in S-phase cells and G2-phase arrest. Additional study indicated that miR-129-5p impaired cell cycle-related genes in 3T3-L1 preadipocytes. Importantly, it showed that miR-129-5p directly targeted the 3'UTR of G3BP1 and the expression of G3BP1 was inhibited by miR-129-5p mimic. Moreover, miR-129-5p mimic activated the p38 signaling pathway through up-regulating p38 and the phosphorylation level of p38. In a word, results in our study revealed that miR-129-5p suppressed preadipocyte proliferation via targeting G3BP1 and activating the p38 signaling pathway.
微小RNA被认为在包括前脂肪细胞在内的不同细胞类型的增殖中起关键作用。在我们的研究中,我们观察到在3T3-L1前脂肪细胞增殖过程中miR-129-5p表达下调,而G3BP1的表达呈现相反的趋势。5-乙炔基-2'-脱氧尿苷(EdU)掺入试验和流式细胞术表明,miR-129-5p的过表达可导致S期细胞减少和G2期阻滞。进一步研究表明,miR-129-5p损害3T3-L1前脂肪细胞中与细胞周期相关的基因。重要的是,研究表明miR-129-5p直接靶向G3BP1的3'非翻译区,并且miR-129-5p模拟物抑制G3BP1的表达。此外,miR-129-5p模拟物通过上调p38及其磷酸化水平激活p38信号通路。总之,我们的研究结果表明,miR-129-5p通过靶向G3BP1并激活p38信号通路抑制前脂肪细胞增殖。