核受体
甾醇调节元件结合蛋白
生物
孤儿受体
肝X受体
转录因子
神经元源性孤儿受体1
胆固醇
甾醇
甲戊酸途径
生物化学
受体
细胞生物学
酶
生物合成
基因
作者
Joyce J. Repa,David J. Mangelsdorf
标识
DOI:10.1146/annurev.cellbio.16.1.459
摘要
▪ Abstract Cholesterol balance is maintained by a series of regulatory pathways that control the acquisition of cholesterol from endogenous and exogenous sources and the elimination of cholesterol, facilitated by its conversion to bile acids. Over the past decade, investigators have discovered that a family of membrane-bound transcription factors, sterol regulatory element-binding proteins (SREBPs), mediate the end-product repression of key enzymes of cholesterol biosynthesis. Recently orphan members of another family of transcription factors, the nuclear hormone receptors, have been found to regulate key pathways in bile acid metabolism, thereby controlling cholesterol elimination. The study of these orphan nuclear receptors suggests their potential as targets for new drug therapies.
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