Wnt Signaling: From Mesenchymal Cell Fate to Lipogenesis and Other Mature Adipocyte Functions

被引:30
|
作者
Bagchi, Devika P. [1 ]
MacDougald, Ormond A. [1 ,2 ]
机构
[1] Univ Michigan, Med Sch, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Med Sch, Dept Internal Med, Div Metab Endocrinol & Diabet, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
PATHWAY EFFECTOR TCF7L2; BETA-CATENIN; BONE-MASS; ADIPOSE-TISSUE; ADIPOGENESIS; GENE; MUTATIONS; OSTEOBLASTOGENESIS; ASSOCIATION; ANTAGONIST;
D O I
10.2337/dbi20-0015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Wnt signaling is an ancient and evolutionarily conserved pathway with fundamental roles in the development of adipose tissues. Roles of this pathway in mesenchymal stem cell fate determination and differentiation have been extensively studied. Indeed, canonical Wnt signaling is a significant endogenous inhibitor of adipogenesis and promoter of other cell fates, including osteogenesis, chondrogenesis, and myogenesis. However, emerging genetic evidence in both humans and mice suggests central roles for Wnt signaling in body fat distribution, obesity, and metabolic dysfunction. Herein, we highlight recent studies that have begun to unravel the contributions of various Wnt pathway members to critical adipocyte functions, including carbohydrate and lipid metabolism. We further explore compelling evidence of complex and coordinated interactions between adipocytes and other cell types within adipose tissues, including stromal, immune, and endothelial cells. Given the evolutionary conservation and ubiquitous cellular distribution of this pathway, uncovering the contributions of Wnt signaling to cell metabolism has exciting implications for therapeutic intervention in widespread pathologic states, including obesity, diabetes, and cancers.
引用
收藏
页码:1419 / 1430
页数:12
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