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CTGF/CCN2 activates canonical Wnt signalling in mesangial cells through LRP6: Implications for the pathogenesis of diabetic nephropathy

机译:CTGF / CCN2通过LRP6激活肾小球系膜细胞中的经典Wnt信号传导:对糖尿病肾病发病机制的影响

摘要

We describe the activation of Wnt signalling in mesangial cells by CCN2. CCN2 stimulates phosphorylation of LRP6 and GSK-3 beta resulting in accumulation and nuclear localisation of beta-catenin, TCF/LEF activity and expression of Wnt targets. This is coincident with decreased phosphorylation of beta-catenin on Ser 33/37 and increased phosphorylation on Tyr142. DKK-1 and LRP6 siRNA reversed CCN2's effects. Microarray analyses of diabetic patients identified differentially expressed Wnt components. beta-Catenin is increased in type 1 diabetic and UUO mice and in in vitro models of hyperglycaemia and hypertension. These findings suggest that Wnt/CCN2 signalling plays a role in the pathogenesis of diabetic nephropathy. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
机译:我们描述了由CCN2在系膜细胞中Wnt信号的激活。 CCN2刺激LRP6和GSK-3 beta的磷酸化,导致β-catenin的积累和核定位,TCF / LEF活性以及Wnt靶标的表达。这与Ser 33/37上β-catenin的磷酸化减少和Tyr142上的磷酸化增加相吻合。 DKK-1和LRP6 siRNA逆转了CCN2的作用。糖尿病患者的微阵列分析鉴定出差异表达的Wnt成分。 β1连环蛋白在1型糖尿病和UUO小鼠以及高血糖和高血压的体外模型中增加。这些发现表明,Wnt / CCN2信号传导在糖尿病性肾病的发病机理中起作用。 (C)2011年欧洲生物化学学会联合会。由Elsevier B.V.发布。保留所有权利。

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