Deletion of Cavin/PTRF Causes Global Loss of Caveolae, Dyslipidemia, and Glucose Intolerance

被引:281
作者
Liu, Libin [1 ]
Brown, Dennis [2 ,3 ,4 ]
McKee, Mary [2 ,3 ,4 ]
LeBrasseur, Nathan K. [5 ]
Yang, Dan [1 ]
Albrecht, Kenneth H. [6 ,7 ]
Ravid, Katya [1 ]
Pilch, Paul F. [1 ]
机构
[1] Boston Univ, Sch Med, Dept Biochem, Boston, MA 02118 USA
[2] Massachusetts Gen Hosp, Ctr Syst Biol, Program Membrane Biol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Div Nephrol, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA 02114 USA
[5] Boston Univ, Sch Med, Dept Med, Sect Endocrinol Diabet & Nutr, Boston, MA 02118 USA
[6] Boston Univ, Sch Med, Dept Med, Genet Program, Boston, MA 02118 USA
[7] Boston Univ, Sch Med, Dept Genet & Genom, Boston, MA 02118 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.cmet.2008.07.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Caveolae are specialized invaginations of the plasma membrane found in numerous cell types. They have been implicated as playing a role in a variety of physiological processes and are typically characterized by their association with the caveolin family of proteins. We show here by means of targeted gene disruption in mice that a distinct caveolae-associated protein, Cavin/PTRF, is an essential component of caveolae. Animals lacking Cavin have no morphologically detectable caveolae in any cell type examined and have markedly diminished protein expression of all three caveolin isoforms while retaining normal or above normal caveolin mRNA expression. Cavin-knockout mice are viable and of normal weight but have higher circulating triglyceride levels, significantly reduced adipose tissue mass, glucose intolerance, and hyperinsulinemia-characteristics that constitute a lipodystrophic phenotype. Our results underscore the multiorgan role of caveolae in metabolic regulation and the obligate presence of Cavin for caveolae formation.
引用
收藏
页码:310 / 317
页数:8
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