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SR-BI是体内微绒毛通道形成以及高密度脂蛋白颗粒定位于肾上腺皮质细胞表面所必需的。

SR-BI is required for microvillar channel formation and the localization of HDL particles to the surface of adrenocortical cells in vivo.

作者信息

Williams David L, Wong Jinny S, Hamilton Robert L

机构信息

Department of Pharmacological Sciences, University Medical Center, State University of New York, Stony Brook, NY 11794, USA.

出版信息

J Lipid Res. 2002 Apr;43(4):544-9.

PMID:11907136
Abstract

Scavenger receptor class B type I (SR-BI) mediates the selective uptake of HDL cholesteryl ester into liver and steroidogenic tissues. In steroidogenic cells, juxtaposed microvilli, or microvilli snuggled against the plasma membrane create microvillar channels that fill with HDL. Microvillar membranes contain SR-BI and are believed to be the site of HDL cholesteryl ester uptake. A recent study showed that SR-BI expression in insect cells elicits membrane structures that contain SR-BI, bind HDL, and closely resemble the ultrastructure of microvillar channels. In the present study we compared the ultrastructure of adrenal gland microvillar membranes in Srb1+/+ and Srb1-/- mice to test whether SR-BI is required for the formation of microvillar channels. The results show that SR-BI is absolutely required for microvillar channel formation and that the microvillar membranes of Srb1-/- mice are 17% thinner than in Srb1+/+ mice. We conclude that SR-BI has a major influence on plasma membrane ultrastructure and organization in vivo.

摘要

I型清道夫受体B类(SR-BI)介导高密度脂蛋白胆固醇酯选择性摄取到肝脏和类固醇生成组织中。在类固醇生成细胞中,并列的微绒毛,或紧贴质膜的微绒毛形成充满高密度脂蛋白的微绒毛通道。微绒毛膜含有SR-BI,被认为是高密度脂蛋白胆固醇酯摄取的部位。最近一项研究表明,昆虫细胞中SR-BI的表达引发了含有SR-BI、结合高密度脂蛋白且与微绒毛通道超微结构极为相似的膜结构。在本研究中,我们比较了Srb1+/+和Srb1-/-小鼠肾上腺微绒毛膜的超微结构,以测试微绒毛通道的形成是否需要SR-BI。结果表明,微绒毛通道的形成绝对需要SR-BI,且Srb1-/-小鼠的微绒毛膜比Srb1+/+小鼠的薄17%。我们得出结论,SR-BI对体内质膜的超微结构和组织有重大影响。

相似文献

1
SR-BI is required for microvillar channel formation and the localization of HDL particles to the surface of adrenocortical cells in vivo.SR-BI是体内微绒毛通道形成以及高密度脂蛋白颗粒定位于肾上腺皮质细胞表面所必需的。
J Lipid Res. 2002 Apr;43(4):544-9.
2
Expression of scavenger receptor class B type 1 (SR-BI) promotes microvillar channel formation and selective cholesteryl ester transport in a heterologous reconstituted system.清道夫受体B1类(SR-BI)的表达在异源重组系统中促进微绒毛通道形成和选择性胆固醇酯转运。
Proc Natl Acad Sci U S A. 2001 Feb 13;98(4):1613-8. doi: 10.1073/pnas.98.4.1613.
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Expression and microvillar localization of scavenger receptor, class B, type I (a high density lipoprotein receptor) in luteinized and hormone-desensitized rat ovarian models.I型清道夫受体B类(一种高密度脂蛋白受体)在黄体化和激素脱敏大鼠卵巢模型中的表达及微绒毛定位
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SR-BI and HDL cholesteryl ester metabolism.SR-BI与高密度脂蛋白胆固醇酯代谢
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Apolipoprotein A-I is necessary for the in vivo formation of high density lipoprotein competent for scavenger receptor BI-mediated cholesteryl ester-selective uptake.载脂蛋白A-I是体内形成能被清道夫受体BI介导的胆固醇酯选择性摄取的高密度脂蛋白所必需的。
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Comparison of class B scavenger receptors, CD36 and scavenger receptor BI (SR-BI), shows that both receptors mediate high density lipoprotein-cholesteryl ester selective uptake but SR-BI exhibits a unique enhancement of cholesteryl ester uptake.B类清道夫受体、CD36和清道夫受体BI(SR-BI)的比较表明,这两种受体均介导高密度脂蛋白胆固醇酯的选择性摄取,但SR-BI对胆固醇酯摄取具有独特的增强作用。
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Scavenger receptor BI (SR-BI) clustered on microvillar extensions suggests that this plasma membrane domain is a way station for cholesterol trafficking between cells and high-density lipoprotein.聚集在微绒毛延伸部分的清道夫受体BI(SR-BI)表明,这个质膜结构域是细胞与高密度脂蛋白之间胆固醇转运的一个中转站。
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Simultaneous induction of an HDL receptor protein (SR-BI) and the selective uptake of HDL-cholesteryl esters in a physiologically relevant steroidogenic cell model.在一个生理相关的类固醇生成细胞模型中同时诱导高密度脂蛋白受体蛋白(SR-BI)以及选择性摄取高密度脂蛋白胆固醇酯。
J Lipid Res. 1998 Aug;39(8):1616-28.
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Expression and microvillar localization of scavenger receptor class B, type I (SR-BI) and selective cholesteryl ester uptake in Leydig cells from rat testis.大鼠睾丸间质细胞中I型清道夫受体B类(SR-BI)的表达、微绒毛定位及胆固醇酯的选择性摄取
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Scavenger receptor class B, type I (SR-BI) is the major route for the delivery of high density lipoprotein cholesterol to the steroidogenic pathway in cultured mouse adrenocortical cells.I型清道夫受体B类(SR-BI)是培养的小鼠肾上腺皮质细胞中高密度脂蛋白胆固醇进入类固醇生成途径的主要途径。
Proc Natl Acad Sci U S A. 1997 Dec 9;94(25):13600-5. doi: 10.1073/pnas.94.25.13600.

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