Nursing Department, Xianyang Central Hospital, Xianyang, China.
CPC Committee, The First People's Hospital of Xianyang, Xianyang, China.
Arch Physiol Biochem. 2020 Dec;126(5):468-475. doi: 10.1080/13813455.2020.1817094. Epub 2020 Sep 29.
The present study aimed to investigate the function and mechanisms of PAR2 in preadipocyte differentiation. This study found that the expression level of PAR2 was increased during 3T3-L1 mouse preadipocyte differentiation towards adipocytes. In addition, PAR2 overexpression significantly stimulated the expression of adipogenic proteins including ACC1, PPARγ, and SREBF1. Moreover, PAR2 overexpression increased the content of triglyceride (TG) in 3T3-L1 preadipocytes. Knockdown of PAR2 suppressed 3T3-L1 preadipocyte differentiation and adipogenesis. Mechanistically, PAR2 promoted 3T3-L1 preadipocyte differentiation and TG production through activation of the PI3K/AKT signalling pathway and gene expression. The research sheds light on the adipogenic effects of PAR2 and its underlying mechanisms. Thus, PAR2 may have therapeutic significance for obesity.
本研究旨在探讨 PAR2 在人前脂肪细胞分化中的功能和机制。本研究发现,PAR2 的表达水平在前脂肪细胞向脂肪细胞分化过程中增加。此外,PAR2 的过表达显著刺激了包括 ACC1、PPARγ 和 SREBF1 在内的脂肪生成蛋白的表达。此外,PAR2 的过表达增加了 3T3-L1 前脂肪细胞中甘油三酯 (TG) 的含量。PAR2 的敲低抑制了 3T3-L1 前脂肪细胞的分化和脂肪生成。在机制上,PAR2 通过激活 PI3K/AKT 信号通路和基因表达促进 3T3-L1 前脂肪细胞的分化和 TG 生成。该研究揭示了 PAR2 的脂肪生成作用及其潜在机制。因此,PAR2 可能对肥胖症具有治疗意义。