Metzger D, Imai T, Jiang M, Takukawa R, Desvergne B, Wahli W, Chambon P
Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) INSERM/CNRS/ULP, 1, rue Laurent Fries, 67404 ILLKIRCH, France.
Prostaglandins Leukot Essent Fatty Acids. 2005 Jul;73(1):51-8. doi: 10.1016/j.plefa.2005.04.007.
The peroxisome proliferator-activated receptor gamma (PPARgamma) is abundantly expressed in adipocytes, and plays an important role in adipocyte differentiation and fat accretion. It is a heterodimeric partner of the retinoid X receptors alpha, beta and gamma, which are also expressed in the adipose tissue. As lethality of PPARgamma(-/-) and RXRalpha(-/-) mouse fetuses precluded the analysis of PPARgamma and RXRalpha functions in mature adipocytes, we generated RXRalpha(ad-/-) and PPARgamma(ad-/-) mice, in which RXRalpha and PPARgamma are selectively ablated in adult adipocytes, respectively. Even though the adiposity of RXRalpha(ad-/-) mice is similar to that of control mice when fed a regular diet, they are resistant to chemically and dietary-induced obesity. However, mature adipocytes lacking either both RXRalpha and RXRgamma or PPARgamma die, and are replaced by newly formed adipocytes. Thus, in adipocytes, RXRalpha is essential for lipogenesis, but RXRgamma can functionally replace RXRalpha for the adipocyte vital functions exerted by PPARgamma/RXR heterodimers.
过氧化物酶体增殖物激活受体γ(PPARγ)在脂肪细胞中大量表达,在脂肪细胞分化和脂肪蓄积中起重要作用。它是视黄酸X受体α、β和γ的异二聚体伴侣,这些受体也在脂肪组织中表达。由于PPARγ(-/-)和RXRα(-/-)小鼠胎儿的致死性妨碍了对成熟脂肪细胞中PPARγ和RXRα功能的分析,我们构建了RXRα(ad-/-)和PPARγ(ad-/-)小鼠,其中RXRα和PPARγ分别在成年脂肪细胞中被选择性敲除。尽管RXRα(ad-/-)小鼠在喂食常规饮食时的肥胖程度与对照小鼠相似,但它们对化学诱导和饮食诱导的肥胖具有抗性。然而,缺乏RXRα和RXRγ或PPARγ的成熟脂肪细胞会死亡,并被新形成的脂肪细胞取代。因此,在脂肪细胞中,RXRα对脂肪生成至关重要,但RXRγ可以在功能上替代RXRα,以实现PPARγ/RXR异二聚体发挥的脂肪细胞重要功能。