PTEN公司
张力素
脂肪生成
生物
蛋白激酶B
脂肪酸合酶
内科学
内分泌学
PI3K/AKT/mTOR通路
癌症研究
磷酸酶
信号转导
细胞生物学
脂质代谢
磷酸化
医学
作者
Jun Hao,Lin Zhu,Zhao Song,Shuxia Liu,Qingjuan Liu,Huijun Duan
标识
DOI:10.1016/j.yexcr.2011.02.003
摘要
Phosphatase and tensin homology deleted on chromosome ten (PTEN) is a negative regulator of PI3K/Akt pathway, and here we investigated the effect of PTEN on lipogenesis in diabetic rats and high glucose-stimulated human renal proximal tubular cell line (HKC). Decreased PTEN and increased phospho-Akt were found in kidney of diabetic rats, and in vitro research revealed that high glucose attenuated PTEN expression in a time-dependent manner, concomitant with activation of Akt. Again, expression of PTEN significantly inhibited high glucose-caused increased phospho-Akt and lipogenic genes including SREBP-1, fatty acid synthase (FASN) and acetyl-CoA carboxylase (ACC). Furthermore, we confirmed inhibition of TGF-β1 pathway with SB431542 blocked the effect of high glucose on PTEN down-regulation, an increase in phospho-Akt and lipogenesis. These above data suggest that decreased PTEN mediates high glucose-induced lipogenesis in renal proximal tubular cells and TGF-β1 might be involved in PTEN down-regulation.
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