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The effect of pleiotrophin signaling on adipogenesis
Authors:Gu Dayong  Yu Bing  Zhao Chen  Ye Wenbin  Lv Qing  Hua Zhong  Ma Jiangan  Zhang Yaou
Affiliation:Life Science Division, Graduate School at Shenzhen, Tsinghua University, Room 407, Building L, Tsinghua Campus, University Town, Shenzhen, Guangdong 518055, PR China.
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.
Keywords:PTN, pleiotrophin   GSK-3β, glycogen synthase kinase 3β   PPARγ, peroxisome proliferator-activated receptor γ   M, methylisobutylxanthine   D, dexamethasone   I, insulin   RTPT, receptor protein tyrosine phosphatase   Fz, frizzled receptor   LRP, low density lipoprotein receptor-related protein   TCF/LEF, T-cell factor/lymphoid-enhancing factor   PI3K, phosphoinositide 3-kinase   GRE, glucocorticoid response element
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