Rigotti A, Edelman E R, Seifert P, Iqbal S N, DeMattos R B, Temel R E, Krieger M, Williams D L
Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
J Biol Chem. 1996 Dec 27;271(52):33545-9. doi: 10.1074/jbc.271.52.33545.
The class B, type I scavenger receptor, SR-BI, binds high density lipoprotein (HDL) and can mediate selective uptake of HDL cholesteryl esters by cultured cells. The high levels of expression of SR-BI in steroidogenic tissues and the importance of selective uptake from HDL as a source of cholesterol for steroidogenesis raised the possibility that SR-BI may participate in cholesterol delivery to steroidogenic tissues in vivo. We have used immunoblotting and immunohistochemical methods to show that SR-BI is specifically expressed in a distinctive pattern on the surfaces of steroid-producing cells in the murine adrenal gland's cortex and that its expression in vivo is induced by adrenocorticotropic hormone and suppressed by glucocorticoids. Thus, expression of SR-BI protein is coordinately regulated with adrenal steroidogenesis. These data provide strong support for the hypothesis that SR-BI is a physiologically relevant HDL receptor that provides substrate cholesterol for steroid hormone synthesis.
B类I型清道夫受体SR-BI可结合高密度脂蛋白(HDL),并能介导培养细胞对HDL胆固醇酯的选择性摄取。SR-BI在类固醇生成组织中的高表达水平以及HDL选择性摄取作为类固醇生成胆固醇来源的重要性,提示SR-BI可能参与体内胆固醇向类固醇生成组织的转运。我们采用免疫印迹和免疫组化方法表明,SR-BI在小鼠肾上腺皮质类固醇生成细胞表面以独特模式特异性表达,其在体内的表达受促肾上腺皮质激素诱导,受糖皮质激素抑制。因此,SR-BI蛋白的表达与肾上腺类固醇生成协同调节。这些数据为SR-BI是一种为类固醇激素合成提供底物胆固醇的生理相关HDL受体这一假说提供了有力支持。