Adipogenesis and WNT signalling

被引:464
作者
Christodoulides, Constantinos [1 ,2 ]
Lagathu, Claire [1 ]
Sethi, Jaswinder K. [1 ]
Vidal-Puig, Antonio [1 ]
机构
[1] Univ Cambridge, Addenbrookes Hosp, Inst Metab Sci, MRC,Ctr Obes & Associated Dis, Cambridge CB2 0QQ, England
[2] Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
ACTIVATED RECEPTOR-GAMMA; ADIPOSE-TISSUE EXPANDABILITY; FRIZZLED-RELATED PROTEIN-1; BETA-CATENIN; BONE MASS; ADIPOCYTE DIFFERENTIATION; INHIBITS ADIPOGENESIS; NEGATIVE REGULATOR; INSULIN-RESISTANCE; OBESITY;
D O I
10.1016/j.tem.2008.09.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An inability of adipose tissue to expand consequent to exhausted capacity to recruit new adipocytes might underlie the association between obesity and insulin resistance. Adipocytes arise from mesenchymal precursors whose commitment and differentiation along the adipocytic lineage is tightly regulated. These regulatory factors mediate cross-talk between adipose cells, ensuring that adipocyte growth and differentiation are coupled to energy storage demands. The WNT family of autocrine and paracrine growth factors regulates adult tissue maintenance and remodelling and, consequently, is well suited to mediate adipose cell communication. Indeed, several recent reports, summarized in this review, implicate WNT signalling in regulating adipogenesis. Manipulating the WNT pathway to alter adipose cellular makeup, therefore, constitutes an attractive drug-development target to combat obesity-associated metabolic complications.
引用
收藏
页码:16 / 24
页数:9
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