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The Class B Scavenger Receptors SR-BI and CD36 Are Receptors for Anionic Phospholipids
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...
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Published in: | The Journal of biological chemistry 1995-07, Vol.270 (27), p.16221-16224 |
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creator | Rigotti, Attilio Acton, Susan L. Krieger, Monty |
description | 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 ~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 ~15 μg 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. |
doi_str_mv | 10.1074/jbc.270.27.16221 |
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Several investigators have described anionic phospholipid binding to cells, and phosphatidylserine (PS) binding to a partially purified ~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 ~15 μg 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.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.270.27.16221</identifier><identifier>PMID: 7541795</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Anions - metabolism ; Antigens, CD - metabolism ; Binding, Competitive ; CD36 Antigens ; Cell Membrane - metabolism ; Cells, Cultured ; Lipoproteins, LDL - metabolism ; Liposomes - metabolism ; Membrane Proteins ; Phosphatidylinositols - metabolism ; Phosphatidylserines - metabolism ; Phospholipids - metabolism ; Receptors, Immunologic - metabolism ; Receptors, Lipoprotein ; Receptors, Scavenger ; Recombinant Proteins - metabolism ; Scavenger Receptors, Class B</subject><ispartof>The Journal of biological chemistry, 1995-07, Vol.270 (27), p.16221-16224</ispartof><rights>1995 © 1995 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-24cbb49a0650381ef977e0a0a6884b07553373c3c46ee5309e35ba2e3ca2c45f3</citedby><cites>FETCH-LOGICAL-c513t-24cbb49a0650381ef977e0a0a6884b07553373c3c46ee5309e35ba2e3ca2c45f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021925817488508$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7541795$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rigotti, Attilio</creatorcontrib><creatorcontrib>Acton, Susan L.</creatorcontrib><creatorcontrib>Krieger, Monty</creatorcontrib><title>The Class B Scavenger Receptors SR-BI and CD36 Are Receptors for Anionic Phospholipids</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>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 ~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 ~15 μg 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.</description><subject>Animals</subject><subject>Anions - metabolism</subject><subject>Antigens, CD - metabolism</subject><subject>Binding, Competitive</subject><subject>CD36 Antigens</subject><subject>Cell Membrane - metabolism</subject><subject>Cells, Cultured</subject><subject>Lipoproteins, LDL - metabolism</subject><subject>Liposomes - metabolism</subject><subject>Membrane Proteins</subject><subject>Phosphatidylinositols - metabolism</subject><subject>Phosphatidylserines - metabolism</subject><subject>Phospholipids - metabolism</subject><subject>Receptors, Immunologic - metabolism</subject><subject>Receptors, Lipoprotein</subject><subject>Receptors, Scavenger</subject><subject>Recombinant Proteins - metabolism</subject><subject>Scavenger Receptors, Class B</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNqFkM9LHDEUx0NR1tX27kXIQXqbbTJJJhNv62p1YcGi29JbyGTeOJHZyTTZVfrfN3YXEUF88HiH7w8eH4SOKZlQIvm3h8pOcknSTmiR5_QTGlNSsowJ-nsPjQnJaaZyUR6gwxgfSBqu6AiNpOBUKjFGv5Yt4FlnYsTn-M6aR-jvIeBbsDCsfYj47jY7n2PT13h2wQo8DfBKbHzA09753ln8o_VxaH3nBlfHz2i_MV2EL7t7hH5-v1zOrrPFzdV8Nl1kVlC2znJuq4orQwpBWEmhUVICMcQUZckrIoVgTDLLLC8ABCMKmKhMDsya3HLRsCP0dds7BP9nA3GtVy5a6DrTg99ELSVTvFT8QyMtVCkZoclItkYbfIwBGj0EtzLhr6ZEPzPXiblOzNPq_8xT5GTXvalWUL8EdpCTfrrVW3ffPrkAunLetrB6W3O2tUEC9ugg6Ggd9BbqFLFrXXv3_g__ANPvmaQ</recordid><startdate>19950707</startdate><enddate>19950707</enddate><creator>Rigotti, Attilio</creator><creator>Acton, Susan L.</creator><creator>Krieger, Monty</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19950707</creationdate><title>The Class B Scavenger Receptors SR-BI and CD36 Are Receptors for Anionic Phospholipids</title><author>Rigotti, Attilio ; Acton, Susan L. ; Krieger, Monty</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-24cbb49a0650381ef977e0a0a6884b07553373c3c46ee5309e35ba2e3ca2c45f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Anions - metabolism</topic><topic>Antigens, CD - metabolism</topic><topic>Binding, Competitive</topic><topic>CD36 Antigens</topic><topic>Cell Membrane - metabolism</topic><topic>Cells, Cultured</topic><topic>Lipoproteins, LDL - metabolism</topic><topic>Liposomes - metabolism</topic><topic>Membrane Proteins</topic><topic>Phosphatidylinositols - metabolism</topic><topic>Phosphatidylserines - metabolism</topic><topic>Phospholipids - metabolism</topic><topic>Receptors, Immunologic - metabolism</topic><topic>Receptors, Lipoprotein</topic><topic>Receptors, Scavenger</topic><topic>Recombinant Proteins - metabolism</topic><topic>Scavenger Receptors, Class B</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rigotti, Attilio</creatorcontrib><creatorcontrib>Acton, Susan L.</creatorcontrib><creatorcontrib>Krieger, Monty</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rigotti, Attilio</au><au>Acton, Susan L.</au><au>Krieger, Monty</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Class B Scavenger Receptors SR-BI and CD36 Are Receptors for Anionic Phospholipids</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1995-07-07</date><risdate>1995</risdate><volume>270</volume><issue>27</issue><spage>16221</spage><epage>16224</epage><pages>16221-16224</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><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 ~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 ~15 μg 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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>7541795</pmid><doi>10.1074/jbc.270.27.16221</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anions - metabolism Antigens, CD - metabolism Binding, Competitive CD36 Antigens Cell Membrane - metabolism Cells, Cultured Lipoproteins, LDL - metabolism Liposomes - metabolism Membrane Proteins Phosphatidylinositols - metabolism Phosphatidylserines - metabolism Phospholipids - metabolism Receptors, Immunologic - metabolism Receptors, Lipoprotein Receptors, Scavenger Recombinant Proteins - metabolism Scavenger Receptors, Class B |
title | The Class B Scavenger Receptors SR-BI and CD36 Are Receptors for Anionic Phospholipids |
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