Gao Jin-Zhi, Zheng Rui-Dan, Wang Cheng-Bin, Ying Yan-Qin, Luo Xiao-Ping
Department of Pediatrics, Huazhong University of Science and Technology, Wuhan, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2011 Oct;13(10):823-6.
This study examined the effects of PI3K inhibitor LY294002 on the differentiation of mouse preadipocytes and the expression of CCAAT enhancer binding protein α (C/EBPα) and peroxisome proliferation activated receptor γ (PPARγ), in order to study the possible roles of insulin receptor substrate (IRSs)/PI3K signal pathway in the differentiation of preadipocytes.
The mouse 3T3-L1 cells were cultured normally and divided into experimental and control groups. 3T3-L1 cells in the experimental group were treated with PI3K inhibitor LY294002 (25 μmol/L) and those in the control group were treated with DMSO culture medium. 3-isobutyl-1-methylxanthine (IBMX) (0.5 mmol/L), dexamethasone (10-6 mol/L) and insulin (5 μg/mL) were used to induce the differentiation of 3T3-L1 preadipocytes in both groups. Before culture, and 2, 4 and 8 days after culture, the cells were collected to detect the expression of C/EBPα and PPARγ by real-time PCR and Western blot assays. The lipid droplets of 3T3-L1 preadipocytes were observed by oil-red O staining.
PI3K inhibitor LY294002 did not affect the expression of C/EBPα and PPARγ in un-induced 3T3-L1 preadipocytes (P>0.05), but decreased the expression of C/EBPα and PPARγ during the in vitro induced differentiation of 3T3-L1 preadipocytes compared with the control group (P<0.05 or 0.01). The lipid droplets count was greatly reduced by LY294002.
PI3K inhibitor LY294002 can inhibit the differentiation of mouse 3T3-LI preadipocytes and the expression of C/EBPα and PPARγ in the differentiation of 3T3-LI preadipoeytes, suggesting that IRSs/PI3K signal pathway may play an important role in the differentiation of 3T3-L1 preadipocytes by regulating the expression of C/EBPα and PPARγ.
本研究检测了PI3K抑制剂LY294002对小鼠前脂肪细胞分化以及CCAAT增强子结合蛋白α(C/EBPα)和过氧化物酶体增殖物激活受体γ(PPARγ)表达的影响,以探讨胰岛素受体底物(IRSs)/PI3K信号通路在前脂肪细胞分化中的可能作用。
将小鼠3T3-L1细胞正常培养并分为实验组和对照组。实验组的3T3-L1细胞用PI3K抑制剂LY294002(25 μmol/L)处理,对照组的细胞用二甲基亚砜培养基处理。两组均使用3-异丁基-1-甲基黄嘌呤(IBMX)(0.5 mmol/L)、地塞米松(10-6 mol/L)和胰岛素(5 μg/mL)诱导3T3-L1前脂肪细胞分化。在培养前以及培养2、4和8天后,收集细胞,通过实时PCR和蛋白质免疫印迹法检测C/EBPα和PPARγ的表达。用油红O染色观察3T3-L1前脂肪细胞的脂滴。
PI3K抑制剂LY294002对未诱导的3T3-L1前脂肪细胞中C/EBPα和PPARγ的表达无影响(P>0.05),但与对照组相比,在体外诱导3T3-L1前脂肪细胞分化过程中,LY294002降低了C/EBPα和PPARγ的表达(P<0.05或0.01)。LY294002使脂滴数量大幅减少。
PI3K抑制剂LY294002可抑制小鼠3T3-L1前脂肪细胞的分化以及3T3-L1前脂肪细胞分化过程中C/EBPα和PPARγ的表达,提示IRSs/PI3K信号通路可能通过调节C/EBPα和PPARγ的表达在3T3-L1前脂肪细胞分化中发挥重要作用。