Shen Joseph J, Huang Lihua, Li Liunan, Jorgez Carolina, Matzuk Martin M, Brown Chester W
Children's Hospital of Central California, Madera, CA 93636, USA.
Mol Endocrinol. 2009 Jan;23(1):113-23. doi: 10.1210/me.2007-0322. Epub 2008 Nov 13.
Growth differentiation factor 3 (GDF3) is a member of the TGFbeta superfamily. White adipose is one of the tissues in which Gdf3 is expressed, and it is the only tissue in which expression increases in response to high-fat diet. We generated Gdf3-/- mice, which were indistinguishable from wild-type mice and had normal weight curves on regular diet. However, on high-fat diet Gdf3-/- mice were resistant to the obesity that normally develops in wild-type mice. Herein we investigate the physiological and molecular mechanisms that underlie this protection from diet-induced obesity and demonstrate that GDF3 deficiency selectively affects white adipose through its influence on basal metabolic rates. Our results are consistent with a role for GDF3 in adipose tissue, with consequential effects on energy expenditure that ultimately impact adiposity.
生长分化因子3(GDF3)是转化生长因子β(TGFβ)超家族的成员之一。白色脂肪是表达Gdf3的组织之一,并且是唯一一种其表达会因高脂饮食而增加的组织。我们培育出了Gdf3基因敲除小鼠,这些小鼠与野生型小鼠没有区别,在正常饮食下体重曲线也正常。然而,在高脂饮食条件下,Gdf3基因敲除小鼠对野生型小鼠通常会出现的肥胖具有抗性。在此,我们研究了这种对饮食诱导肥胖的保护作用背后的生理和分子机制,并证明GDF3缺乏通过影响基础代谢率选择性地影响白色脂肪。我们的结果与GDF3在脂肪组织中的作用一致,其对能量消耗产生影响,最终影响肥胖程度。