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Factor for Adipocyte Differentiation 158 Gene Disruption Prevents the Body Weight Gain and Insulin Resistance Induced by a High-Fat Diet

机译:脂肪细胞分化因子158基因破坏阻止高脂饮食诱导的体重增加和胰岛素抵抗

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摘要

To clarify the molecular mechanism of adipocyte differentiation, we previously isolated a novel gene, factor for adipocyte differentiation (fad) 158, whose expression was induced during the earliest stages of adipogenesis, and its product was localized to the endoplasmic reticulum. We found that the knockdown of fad 158 expression prevented the differentiation of 3T3-L1 cells into adipocytes. In addition, over-expression of fad 158 promoted the differentiation of NIH-3T3 cells, which do not usually differentiate into adipocytes. Although these findings strongly suggest that fad 158 has a crucial role in regulating adipocyte differentiation, the physiological role of the gene is still unclear. In this study, we generated mice in which fad 158 expression was deleted. The fad 158-deficient mice did not show remarkable changes in body weight or the weight of white adipose tissue on a chow diet, but had significantly lower body weights and fat mass than wild-type mice when fed a high-fat diet. Furthermore, although the disruption of fad 158 did not influence insulin sensitivity on the chow diet, it improved insulin resistance induced by the high-fat diet. These results indicate that fad 158 is a key factor in the development of obesity and insulin resistance caused by a high-fat diet.
机译:为了阐明脂肪细胞分化的分子机制,我们先前分离了一个新的基因,即脂肪细胞分化因子(fad)158,其表达在脂肪形成的最早阶段被诱导,其产物定位于内质网。我们发现,敲低fad 158表达阻止了3T3-L1细胞分化成脂肪细胞。此外,fad 158的过表达促进了NIH-3T3细胞的分化,而NIH-3T3细胞通常不分化为脂肪细胞。尽管这些发现强烈表明,fad 158在调节脂肪细胞分化中具有关键作用,但该基因的生理作用仍不清楚。在这项研究中,我们生成了fad 158表达缺失的小鼠。缺乏食物的158型时尚小鼠在日常饮食中的体重或白色脂肪组织的重量均未显示出明显的变化,但是当饲喂高脂饮食时,其体重和脂肪量明显低于野生型小鼠。此外,尽管fad 158的破坏并没有影响食物对胰岛素的敏感性,但它改善了高脂饮食诱导的胰岛素抵抗。这些结果表明,fad 158是由高脂饮食引起的肥胖和胰岛素抵抗发展的关键因素。

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