Targeted disruption of the melanocortin-4 receptor results in obesity in mice

被引:2552
作者
Huszar, D
Lynch, CA
FairchildHuntress, V
Dunmore, JH
Fang, Q
Berkemeier, LR
Gu, W
Kesterson, RA
Boston, BA
Cone, RD
Smith, FJ
Campfield, LA
Burn, P
Lee, F
机构
[1] OREGON HLTH SCI UNIV, VOLLUM INST ADV BIOMED RES, PORTLAND, OR 97201 USA
[2] OREGON HLTH SCI UNIV, DEPT PEDIAT, PORTLAND, OR 97201 USA
[3] HOFFMANN LA ROCHE INC, DEPT METAB DIS, NUTLEY, NJ 07110 USA
关键词
D O I
10.1016/S0092-8674(00)81865-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The melanocortin-4 receptor (MC4-R) is a G protein-coupled, seven-transmembrane receptor expressed in the brain. Inactivation of this receptor by gene targeting results in mice that develop a maturity onset obesity syndrome associated with hyperphagia, hyperinsulinemia, and hyperglycemia. This syndrome recapitulates several of the characteristic features of the agouti obesity syndrome, which results from ectopic expression of agouti protein, a pigmentation factor normally expressed in the skin. Our data identify a novel signaling pathway in the mouse for body weight regulation and support a model in which the primary mechanism by which agouti induces obesity is chronic antagonism of the MC4-R.
引用
收藏
页码:131 / 141
页数:11
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