The long isoform uncoupling protein-3 (UCP3L) in human energy homeostasis

被引:7
作者
Chung, WK
Luke, A
Cooper, RS
Rotini, C
Vidal-Puig, A
Rosenbaum, M
Gordon, D
Leal, SM
Caprio, S
Goldsmith, R
Andreu, AL
Bruno, C
DiMauro, S
Heo, M
Lowe, WL
Lowell, BB
Allison, DB
Leibel, RL
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Pediat, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Med, Div Mol Genet,Naomi Berrie Diabet Ctr, New York, NY 10032 USA
[3] Loyola Univ, Med Ctr, Dept Epidemiol & Prevent Med, Maywood, IL 60153 USA
[4] Rockefeller Univ, New York, NY 10021 USA
[5] Beth Israel Deaconess Med Ctr, Div Endocrinol, Boston, MA 02215 USA
[6] Yale Univ, Sch Med, Div Pediat Endocrinol, New Haven, CT 06510 USA
[7] Columbia Univ, Coll Phys & Surg, St Lukes Roosevelt Hosp Ctr, Obes Res Ctr, New York, NY 10025 USA
[8] Northwestern Univ, Sch Med, Dept Med, Chicago, IL 60611 USA
[9] Columbia Univ Coll Phys & Surg, H Houston Merritt Clin Res Ctr Muscular Dystrophy, New York, NY 10032 USA
关键词
obesity; diabetes; skeletal muscle; thermogenesis;
D O I
10.1038/sj.ijo.0800945
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The biological role(s) proposed for UCP3 in energy homeostasis have been based primarily upon amino acid sequence homology to UCP1. Spontaneous mutations of UCP3> have been described in humans, but not in rodents. The functional consequences-or lack thereof-of these mutations in humans will be of great importance in elucidating the biology of this protein. The results of two such studies are summarized here.
引用
收藏
页码:S49 / S50
页数:2
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