脂肪生成
脂肪细胞
磷酸化
转录因子
过氧化物酶体增殖物激活受体
化学
细胞生物学
脂肪组织
激酶
生物
内分泌学
内科学
受体
生物化学
基因
医学
作者
Erding Hu,Jae Bum Kim,Pasha Sarraf,Bruce M. Spiegelman
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1996-12-20
卷期号:274 (5295): 2100-2103
被引量:1035
标识
DOI:10.1126/science.274.5295.2100
摘要
Adipocyte differentiation is an important component of obesity and other metabolic diseases. This process is strongly inhibited by many mitogens and oncogenes. Several growth factors that inhibit fat cell differentiation caused mitogen-activated protein (MAP) kinase-mediated phosphorylation of the dominant adipogenic transcription factor peroxisome proliferator-activated receptor γ (PPARγ) and reduction of its transcriptional activity. Expression of PPARγ with a nonphosphorylatable mutation at this site (serine-112) yielded cells with increased sensitivity to ligand-induced adipogenesis and resistance to inhibition of differentiation by mitogens. These results indicate that covalent modification of PPARγ by serum and growth factors is a major regulator of the balance between cell growth and differentiation in the adipose cell lineage.
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