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多效生长因子信号传导对脂肪生成的影响。

The effect of pleiotrophin signaling on adipogenesis.

作者信息

Gu Dayong, Yu Bing, Zhao Chen, Ye Wenbin, Lv Qing, Hua Zhong, Ma Jiangan, Zhang Yaou

机构信息

Life Science Division, Graduate School at Shenzhen, Tsinghua University, Room 407, Building L, Tsinghua Campus, University Town, Shenzhen, Guangdong 518055, PR China.

出版信息

FEBS Lett. 2007 Feb 6;581(3):382-8. doi: 10.1016/j.febslet.2006.12.043. Epub 2007 Jan 19.

Abstract

Pleiotrophin (PTN) plays diverse roles in cell growth and differentiation. In this investigation, we demonstrate that PTN plays a negative role in adipogensis and that glycogen synthase kinase 3beta (GSK-3beta) and beta-catenin are involved in the regulation of PTN-mediated preadipocyte differentiation. Knocking down the expression of PTN using siRNA resulted in an increase in phospho-GSK-3beta expression, and the accumulation of nuclear beta-catenin, which are critical downstream signaling proteins for both the PTN and Wnt signaling pathways. Our investigation suggests that there is a PTN/PI3K/AKT/GSK-3beta/beta-catenin signaling pathway, which cross-talks with the Wnt/Fz/GSK-3beta/beta-catenin pathway and negatively regulates adipogenesis.

摘要

多效生长因子(PTN)在细胞生长和分化中发挥多种作用。在本研究中,我们证明PTN在脂肪生成中起负向作用,并且糖原合酶激酶3β(GSK-3β)和β-连环蛋白参与PTN介导的前脂肪细胞分化的调节。使用小干扰RNA(siRNA)敲低PTN的表达导致磷酸化GSK-3β表达增加以及核β-连环蛋白的积累,这两者都是PTN和Wnt信号通路的关键下游信号蛋白。我们的研究表明存在一条PTN/PI3K/AKT/GSK-3β/β-连环蛋白信号通路,该通路与Wnt/Fz/GSK-3β/β-连环蛋白通路相互作用并对脂肪生成起负向调节作用。

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