Lagathu Claire, Christodoulides Constantinos, Virtue Sam, Cawthorn William P, Franzin Chiara, Kimber Wendy A, Nora Edoardo Dalla, Campbell Mark, Medina-Gomez Gema, Cheyette Benjamin N R, Vidal-Puig Antonio J, Sethi Jaswinder K
Institute of Metabolic Science-Metabolic Research Laboratories and Department of Clinical Biochemistry, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
Diabetes. 2009 Mar;58(3):609-19. doi: 10.2337/db08-1180. Epub 2008 Dec 10.
Wnt signaling inhibits adipogenesis, but its regulation, physiological relevance, and molecular effectors are poorly understood. Here, we identify the Wnt modulator Dapper1/Frodo1 (Dact1) as a new preadipocyte gene involved in the regulation of murine and human adipogenesis.
Changes in Dact1 expression were investigated in three in vitro models of adipogenesis. In vitro gain- and loss-of-function studies were used to investigate the mechanism of Dact1 action during adipogenesis. The in vivo regulation of Dact1 and Wnt/beta-catenin signaling were investigated in murine models of altered nutritional status, of pharmacological stimulation of in vivo adipogenesis, and during the development of dietary and genetic obesity.
Dact1 is a preadipocyte gene that decreases during adipogenesis. However, Dact1 knockdown impairs adipogenesis through activation of the Wnt/beta-catenin signaling pathway, and this is reversed by treatment with the secreted Wnt antagonist, secreted Frizzled-related protein 1 (Sfrp1). In contrast, constitutive Dact1 overexpression promotes adipogenesis and confers resistance to Wnt ligand-induced antiadipogenesis through increased expression of endogenous Sfrps and reduced expression of Wnts. In vivo, in white adipose tissue, Dact1 and Wnt/beta-catenin signaling also exhibit coordinated expression profiles in response to altered nutritional status, in response to pharmacological stimulation of in vivo adipogenesis, and during the development of dietary and genetic obesity.
Dact1 regulates adipogenesis through coordinated effects on gene expression that selectively alter intracellular and paracrine/autocrine components of the Wnt/beta-catenin signaling pathway. These novel insights into the molecular mechanisms controlling adipose tissue plasticity provide a functional network with therapeutic potential against diseases, such as obesity and associated metabolic disorders.
Wnt信号传导可抑制脂肪生成,但其调控机制、生理相关性及分子效应器仍知之甚少。在此,我们鉴定出Wnt调节剂Dapper1/Frodo1(Dact1)是一种参与调节小鼠和人类脂肪生成的新型前脂肪细胞基因。
在三种脂肪生成的体外模型中研究了Dact1表达的变化。采用体外功能获得和功能缺失研究来探究Dact1在脂肪生成过程中的作用机制。在营养状况改变、体内脂肪生成的药理刺激以及饮食性和遗传性肥胖发展过程的小鼠模型中,研究了Dact1和Wnt/β-连环蛋白信号传导的体内调控。
Dact1是一种在前脂肪细胞中表达且在脂肪生成过程中降低的基因。然而,Dact1基因敲低通过激活Wnt/β-连环蛋白信号通路损害脂肪生成,而分泌型Wnt拮抗剂分泌型卷曲相关蛋白1(Sfrp1)处理可逆转这种损害。相反,组成型Dact1过表达促进脂肪生成,并通过增加内源性Sfrps的表达和降低Wnts的表达赋予对Wnt配体诱导的抗脂肪生成的抗性。在体内,在白色脂肪组织中,Dact1和Wnt/β-连环蛋白信号传导在营养状况改变、体内脂肪生成的药理刺激以及饮食性和遗传性肥胖发展过程中也表现出协调的表达谱。
Dact1通过对基因表达的协同作用来调节脂肪生成,这些作用选择性地改变Wnt/β-连环蛋白信号通路的细胞内和旁分泌/自分泌成分。这些对控制脂肪组织可塑性分子机制的新见解提供了一个具有治疗肥胖症和相关代谢紊乱等疾病潜力的功能网络。