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Mouse Transferrin Receptor 1 Is the Cell Entry Receptor for Mouse Mammary Tumor Virus
Enveloped viruses enter cells by binding to their entry receptors and fusing with the membrane at the cell surface or after trafficking through acidic endosomal compartments. Species-specific virus tropism is usually determined by these entry receptors. Because mouse mammary tumor virus (MMTV) is un...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2002-09, Vol.99 (19), p.12386-12390 |
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creator | Ross, Susan R. Schofield, Jason J. Farr, Christine J. Bucan, Maja |
description | Enveloped viruses enter cells by binding to their entry receptors and fusing with the membrane at the cell surface or after trafficking through acidic endosomal compartments. Species-specific virus tropism is usually determined by these entry receptors. Because mouse mammary tumor virus (MMTV) is unable to infect Chinese hamster cells, we used phenotypic screening of the T31 mouse/hamster radiation hybrid panel to map the MMTV cell entry receptor gene and subsequently found that it is transferrin receptor 1. MMTV-resistant human cells that expressed mouse transferrin receptor 1 became susceptible to MMTV infection, and treatment of mouse cells with a monoclonal antibody that down-regulated cell surface expression of the receptor blocked infection. MMTV, like vesicular stomatitis virus, depended on acid pH for infection. MMTV may use transferrin receptor 1, a membrane protein that is endocytosed via clathrin-coated pits and traffics through the acidic endosomes, to rapidly get to a compartment where acid pH triggers the conformational changes in envelope protein required for membrane fusion. |
doi_str_mv | 10.1073/pnas.192360099 |
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Species-specific virus tropism is usually determined by these entry receptors. Because mouse mammary tumor virus (MMTV) is unable to infect Chinese hamster cells, we used phenotypic screening of the T31 mouse/hamster radiation hybrid panel to map the MMTV cell entry receptor gene and subsequently found that it is transferrin receptor 1. MMTV-resistant human cells that expressed mouse transferrin receptor 1 became susceptible to MMTV infection, and treatment of mouse cells with a monoclonal antibody that down-regulated cell surface expression of the receptor blocked infection. MMTV, like vesicular stomatitis virus, depended on acid pH for infection. MMTV may use transferrin receptor 1, a membrane protein that is endocytosed via clathrin-coated pits and traffics through the acidic endosomes, to rapidly get to a compartment where acid pH triggers the conformational changes in envelope protein required for membrane fusion.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.192360099</identifier><identifier>PMID: 12218182</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animals ; Biological Sciences ; Cell Line ; Cell lines ; Cell surface receptors ; Cells ; Chromosome Mapping ; Chromosomes, Artificial, Bacterial - genetics ; Cricetinae ; Endosomes ; Humans ; Hybrid Cells ; Infections ; Mammary Tumor Virus, Mouse - pathogenicity ; Mammary Tumor Virus, Mouse - physiology ; Membranes ; Mice ; Microbiology ; Proteins ; Receptors ; Receptors, Transferrin - genetics ; Receptors, Transferrin - physiology ; Receptors, Virus - genetics ; Receptors, Virus - physiology ; Somatic cells ; Transfection ; Transferrins ; Tumors ; Viruses</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2002-09, Vol.99 (19), p.12386-12390</ispartof><rights>Copyright 1993-2002 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Sep 17, 2002</rights><rights>Copyright © 2002, The National Academy of Sciences 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c587t-8282153040d2616906c5ddbb6446299792f70a79b1d7a70a92cabf31fa478f443</citedby><cites>FETCH-LOGICAL-c587t-8282153040d2616906c5ddbb6446299792f70a79b1d7a70a92cabf31fa478f443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/99/19.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3073224$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3073224$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12218182$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ross, Susan R.</creatorcontrib><creatorcontrib>Schofield, Jason J.</creatorcontrib><creatorcontrib>Farr, Christine J.</creatorcontrib><creatorcontrib>Bucan, Maja</creatorcontrib><title>Mouse Transferrin Receptor 1 Is the Cell Entry Receptor for Mouse Mammary Tumor Virus</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Enveloped viruses enter cells by binding to their entry receptors and fusing with the membrane at the cell surface or after trafficking through acidic endosomal compartments. Species-specific virus tropism is usually determined by these entry receptors. Because mouse mammary tumor virus (MMTV) is unable to infect Chinese hamster cells, we used phenotypic screening of the T31 mouse/hamster radiation hybrid panel to map the MMTV cell entry receptor gene and subsequently found that it is transferrin receptor 1. MMTV-resistant human cells that expressed mouse transferrin receptor 1 became susceptible to MMTV infection, and treatment of mouse cells with a monoclonal antibody that down-regulated cell surface expression of the receptor blocked infection. MMTV, like vesicular stomatitis virus, depended on acid pH for infection. MMTV may use transferrin receptor 1, a membrane protein that is endocytosed via clathrin-coated pits and traffics through the acidic endosomes, to rapidly get to a compartment where acid pH triggers the conformational changes in envelope protein required for membrane fusion.</description><subject>Animals</subject><subject>Biological Sciences</subject><subject>Cell Line</subject><subject>Cell lines</subject><subject>Cell surface receptors</subject><subject>Cells</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Artificial, Bacterial - genetics</subject><subject>Cricetinae</subject><subject>Endosomes</subject><subject>Humans</subject><subject>Hybrid Cells</subject><subject>Infections</subject><subject>Mammary Tumor Virus, Mouse - pathogenicity</subject><subject>Mammary Tumor Virus, Mouse - physiology</subject><subject>Membranes</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Proteins</subject><subject>Receptors</subject><subject>Receptors, Transferrin - genetics</subject><subject>Receptors, Transferrin - physiology</subject><subject>Receptors, Virus - genetics</subject><subject>Receptors, Virus - physiology</subject><subject>Somatic cells</subject><subject>Transfection</subject><subject>Transferrins</subject><subject>Tumors</subject><subject>Viruses</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkc1v1DAQxS1ERZfClROCqAfUSxaP7fjjwKFaFajUCgltuVpOYtOs8rG1E9T-90y0yxY4wMGy5fm98Rs_Ql4BXQJV_P22d2kJhnFJqTFPyAKogVwKQ5-SBaVM5VowcUyep7ShiBSaPiPHwBho0GxBbq6HKflsHV2fgo-x6bOvvvLbcYgZZJcpG299tvJtm130Y3x4LAZcO-216zqHpfXU4d23Jk7pBTkKrk3-5X4_ITcfL9arz_nVl0-Xq_OrvCq0GnPNNIOCU0FrJkEaKquirstSCiGZMcqwoKhTpoRaOTwZVrkycAhOKB2E4Cfkw67vdio7X1cePbrWbmMzO7KDa-yflb65td-HHxaYEcWsf7fXx-Fu8mm0XZMqnNb1HmeziuGncrT4PxC0wFFg7nj6F7gZptjjJ1hG8VUFQiK03EFVHFKKPhwcA7VzrHaO1R5iRcGb3-d8xPc5InC2B2bhr7Ix2AMhrqUNU9uO_n5E9O2_USRe74hNwqQPCEdjjAn-Ey-2vp4</recordid><startdate>20020917</startdate><enddate>20020917</enddate><creator>Ross, Susan R.</creator><creator>Schofield, Jason J.</creator><creator>Farr, Christine J.</creator><creator>Bucan, Maja</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20020917</creationdate><title>Mouse Transferrin Receptor 1 Is the Cell Entry Receptor for Mouse Mammary Tumor Virus</title><author>Ross, Susan R. ; Schofield, Jason J. ; Farr, Christine J. ; Bucan, Maja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c587t-8282153040d2616906c5ddbb6446299792f70a79b1d7a70a92cabf31fa478f443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Biological Sciences</topic><topic>Cell Line</topic><topic>Cell lines</topic><topic>Cell surface receptors</topic><topic>Cells</topic><topic>Chromosome Mapping</topic><topic>Chromosomes, Artificial, Bacterial - genetics</topic><topic>Cricetinae</topic><topic>Endosomes</topic><topic>Humans</topic><topic>Hybrid Cells</topic><topic>Infections</topic><topic>Mammary Tumor Virus, Mouse - pathogenicity</topic><topic>Mammary Tumor Virus, Mouse - physiology</topic><topic>Membranes</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Proteins</topic><topic>Receptors</topic><topic>Receptors, Transferrin - genetics</topic><topic>Receptors, Transferrin - physiology</topic><topic>Receptors, Virus - genetics</topic><topic>Receptors, Virus - physiology</topic><topic>Somatic cells</topic><topic>Transfection</topic><topic>Transferrins</topic><topic>Tumors</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ross, Susan R.</creatorcontrib><creatorcontrib>Schofield, Jason J.</creatorcontrib><creatorcontrib>Farr, Christine J.</creatorcontrib><creatorcontrib>Bucan, Maja</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ross, Susan R.</au><au>Schofield, Jason J.</au><au>Farr, Christine J.</au><au>Bucan, Maja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mouse Transferrin Receptor 1 Is the Cell Entry Receptor for Mouse Mammary Tumor Virus</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2002-09-17</date><risdate>2002</risdate><volume>99</volume><issue>19</issue><spage>12386</spage><epage>12390</epage><pages>12386-12390</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Enveloped viruses enter cells by binding to their entry receptors and fusing with the membrane at the cell surface or after trafficking through acidic endosomal compartments. Species-specific virus tropism is usually determined by these entry receptors. Because mouse mammary tumor virus (MMTV) is unable to infect Chinese hamster cells, we used phenotypic screening of the T31 mouse/hamster radiation hybrid panel to map the MMTV cell entry receptor gene and subsequently found that it is transferrin receptor 1. MMTV-resistant human cells that expressed mouse transferrin receptor 1 became susceptible to MMTV infection, and treatment of mouse cells with a monoclonal antibody that down-regulated cell surface expression of the receptor blocked infection. MMTV, like vesicular stomatitis virus, depended on acid pH for infection. 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subjects | Animals Biological Sciences Cell Line Cell lines Cell surface receptors Cells Chromosome Mapping Chromosomes, Artificial, Bacterial - genetics Cricetinae Endosomes Humans Hybrid Cells Infections Mammary Tumor Virus, Mouse - pathogenicity Mammary Tumor Virus, Mouse - physiology Membranes Mice Microbiology Proteins Receptors Receptors, Transferrin - genetics Receptors, Transferrin - physiology Receptors, Virus - genetics Receptors, Virus - physiology Somatic cells Transfection Transferrins Tumors Viruses |
title | Mouse Transferrin Receptor 1 Is the Cell Entry Receptor for Mouse Mammary Tumor Virus |
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