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B类清道夫受体SR-BI和CD36是阴离子磷脂的受体。

The class B scavenger receptors SR-BI and CD36 are receptors for anionic phospholipids.

作者信息

Rigotti A, Acton S L, Krieger M

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

J Biol Chem. 1995 Jul 7;270(27):16221-4. doi: 10.1074/jbc.270.27.16221.

Abstract

The specific recognition of anionic phospholipids in the outer leaflets of cell membranes and lipoproteins by cell surface receptors may play an important role in a variety of physiologic and pathophysiologic processes (e.g. recognition of damaged or senescent cells by the reticuloendothelial system or lipoprotein homeostasis). Several investigators have described anionic phospholipid binding to cells, and phosphatidylserine (PS) binding to a partially purified approximately 95-kDa membrane protein has recently been reported (Sambrano, G.R., and Steinberg, D. (1995) Proc. Natl. Acad. Sci. U.S.A. 92, 1396-1400). Using both direct binding and ligand competition assays in transfected cells, we have found that two class B scavenger receptors, SR-BI and CD36, can tightly bind PS and phosphatidylinositol (PI)-containing liposomes (Kd for PS liposome binding to SR-BI is approximately 15 micrograms phospholipid/ml or 0.18 nM (mol PS liposomes/l), but not phosphatidylcholine, phosphatidylethanolamine, or sphingomyelin liposomes. PS and PI liposomes, but not the others, could effectively compete with PS liposomes and modified or native lipoproteins for binding to these receptors. Phosphatidic acid, another anionic phospholipid, could also compete, but was not as effective as PS or PI. Class B scavenger receptors are the first molecularly well-defined, specific cell surface receptors for anionic phospholipids to be described.

摘要

细胞表面受体对细胞膜和脂蛋白外小叶中阴离子磷脂的特异性识别可能在多种生理和病理生理过程中发挥重要作用(例如网状内皮系统对受损或衰老细胞的识别或脂蛋白稳态)。几位研究者描述了阴离子磷脂与细胞的结合,最近有报道称磷脂酰丝氨酸(PS)与一种部分纯化的约95 kDa膜蛋白结合(Sambrano, G.R., and Steinberg, D. (1995) Proc. Natl. Acad. Sci. U.S.A. 92, 1396 - 1400)。通过在转染细胞中使用直接结合和配体竞争试验,我们发现两种B类清道夫受体,SR - BI和CD36,可以紧密结合含PS和磷脂酰肌醇(PI)的脂质体(PS脂质体与SR - BI结合的Kd约为15微克磷脂/毫升或0.18纳摩尔(摩尔PS脂质体/升)),但不能结合磷脂酰胆碱、磷脂酰乙醇胺或鞘磷脂脂质体。PS和PI脂质体,而非其他脂质体,能够有效地与PS脂质体以及修饰或天然脂蛋白竞争结合这些受体。另一种阴离子磷脂磷脂酸也能竞争,但不如PS或PI有效。B类清道夫受体是首个在分子层面被明确界定的、特异性识别阴离子磷脂的细胞表面受体。

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