Compensation by the muscle limits the metabolic consequences of lipodystrophy in PPARγ hypomorphic mice

Hana Koutnikova, Terrie Anne Cock, Mitsuhiro Watanabe, Sander M. Houten, Marie France Champy, Andrée Dierich, Johan Auwerx

研究成果: Article査読

148 被引用数 (Scopus)

抄録

Peroxisome proliferator-activated receptor γ (PPARγ) is a nuclear receptor, which controls adipocyte differentiation. We targeted with homologous recombination the PPARγ2-specific exon B, resulting in a white adipose tissue knockdown of PPARγ. Although homozygous (PPARγ hyp/hyp) mice are born with similar weight as the WT mice, the PPARγhyp/hyp animals become growth retarded and develop severe lipodystrophy and hyperlipidemia. Almost half of these PPARγ hyp/hyp mice die before adulthood, whereas the surviving PPARγhyp/hyp animals overcome the growth retardation, yet remain lipodystrophic. In contrast to most lipodystrophic models, the adult PPARγhyp/hyp mice only have mild glucose intolerance and do not have a fatty liver. These metabolic consequences of the lipodystrophy are relatively benign because of the induction of a compensatory gene expression program in the muscle that enables efficient oxidation of excess lipids. The PPARγhyp/hyp mice unequivocally demonstrate that PPARγ is the master regulator of adipogenesis in vivo and establish that lipid and glucose homeostasis can be relatively well maintained in the absence of white adipose tissue.

本文言語English
ページ(範囲)14457-14462
ページ数6
ジャーナルProceedings of the National Academy of Sciences of the United States of America
100
SUPPL. 2
DOI
出版ステータスPublished - 2003 11 25
外部発表はい

ASJC Scopus subject areas

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