Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Proceedings of the National Academy of Sciences - PNAS 2002-09, Vol.99 (19), p.12386-12390
Main Authors: Ross, Susan R., Schofield, Jason J., Farr, Christine J., Bucan, Maja
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c587t-8282153040d2616906c5ddbb6446299792f70a79b1d7a70a92cabf31fa478f443
cites cdi_FETCH-LOGICAL-c587t-8282153040d2616906c5ddbb6446299792f70a79b1d7a70a92cabf31fa478f443
container_end_page 12390
container_issue 19
container_start_page 12386
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 99
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
format article
fullrecord <record><control><sourceid>jstor_pubme</sourceid><recordid>TN_cdi_pubmed_primary_12218182</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>3073224</jstor_id><sourcerecordid>3073224</sourcerecordid><originalsourceid>FETCH-LOGICAL-c587t-8282153040d2616906c5ddbb6446299792f70a79b1d7a70a92cabf31fa478f443</originalsourceid><addsrcrecordid>eNqFkc1v1DAQxS1ERZfClROCqAfUSxaP7fjjwKFaFajUCgltuVpOYtOs8rG1E9T-90y0yxY4wMGy5fm98Rs_Ql4BXQJV_P22d2kJhnFJqTFPyAKogVwKQ5-SBaVM5VowcUyep7ShiBSaPiPHwBho0GxBbq6HKflsHV2fgo-x6bOvvvLbcYgZZJcpG299tvJtm130Y3x4LAZcO-216zqHpfXU4d23Jk7pBTkKrk3-5X4_ITcfL9arz_nVl0-Xq_OrvCq0GnPNNIOCU0FrJkEaKquirstSCiGZMcqwoKhTpoRaOTwZVrkycAhOKB2E4Cfkw67vdio7X1cePbrWbmMzO7KDa-yflb65td-HHxaYEcWsf7fXx-Fu8mm0XZMqnNb1HmeziuGncrT4PxC0wFFg7nj6F7gZptjjJ1hG8VUFQiK03EFVHFKKPhwcA7VzrHaO1R5iRcGb3-d8xPc5InC2B2bhr7Ix2AMhrqUNU9uO_n5E9O2_USRe74hNwqQPCEdjjAn-Ey-2vp4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>201297146</pqid></control><display><type>article</type><title>Mouse Transferrin Receptor 1 Is the Cell Entry Receptor for Mouse Mammary Tumor Virus</title><source>PubMed Central</source><source>JSTOR</source><creator>Ross, Susan R. ; Schofield, Jason J. ; Farr, Christine J. ; Bucan, Maja</creator><creatorcontrib>Ross, Susan R. ; Schofield, Jason J. ; Farr, Christine J. ; Bucan, Maja</creatorcontrib><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><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 &amp; 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. 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.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>12218182</pmid><doi>10.1073/pnas.192360099</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0027-8424
ispartof Proceedings of the National Academy of Sciences - PNAS, 2002-09, Vol.99 (19), p.12386-12390
issn 0027-8424
1091-6490
language eng
recordid cdi_pubmed_primary_12218182
source PubMed Central; JSTOR
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T17%3A14%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mouse%20Transferrin%20Receptor%201%20Is%20the%20Cell%20Entry%20Receptor%20for%20Mouse%20Mammary%20Tumor%20Virus&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Ross,%20Susan%20R.&rft.date=2002-09-17&rft.volume=99&rft.issue=19&rft.spage=12386&rft.epage=12390&rft.pages=12386-12390&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/10.1073/pnas.192360099&rft_dat=%3Cjstor_pubme%3E3073224%3C/jstor_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c587t-8282153040d2616906c5ddbb6446299792f70a79b1d7a70a92cabf31fa478f443%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=201297146&rft_id=info:pmid/12218182&rft_jstor_id=3073224&rfr_iscdi=true