CD46 on glial cells can function as a receptor for viral glycoprotein-mediated cell-cell fusion
Membrane cofactor protein (CD46) is a regulator of complement activation that also serves as the entry receptor for human herpes virus 6 (HHV‐6) and measles virus (MV) into human cells. While it is clear that oligodendrocytes and astrocytes are cell types commonly infected by these viruses, it is un...
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Veröffentlicht in: | Glia 2005-11, Vol.52 (3), p.252-258 |
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creator | Cassiani-Ingoni, Riccardo Greenstone, Heather L. Donati, Donatella Fogdell-Hahn, Anna Martinelli, Elena Refai, Daniel Martin, Roland Berger, Edward A. Jacobson, Steven |
description | Membrane cofactor protein (CD46) is a regulator of complement activation that also serves as the entry receptor for human herpes virus 6 (HHV‐6) and measles virus (MV) into human cells. While it is clear that oligodendrocytes and astrocytes are cell types commonly infected by these viruses, it is unclear whether oligodendrocytes express CD46, or which are the cellular mechanisms underlying the infection. We show that adult oligodendrocytes, as well as astrocytes and microglial cells, express CD46 on the cellular surface. Moreover, we employed a quantitative fusion assay to demonstrate that HHV‐6A infection of T lymphocytes enables cell–cell fusion of these cells to astrocytes or to oligodendroglial cells. This fusion is mediated by the interaction between viral glycoproteins expressed on the membrane of the infected cells and CD46 on the glial targets, and is also observed using cells expressing recombinant MV glycoproteins. These data suggest a mechanism that involves cell–cell fusion by which certain viruses could spread the infection from the periphery to the cells in the nervous system. Published 2005 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/glia.20219 |
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While it is clear that oligodendrocytes and astrocytes are cell types commonly infected by these viruses, it is unclear whether oligodendrocytes express CD46, or which are the cellular mechanisms underlying the infection. We show that adult oligodendrocytes, as well as astrocytes and microglial cells, express CD46 on the cellular surface. Moreover, we employed a quantitative fusion assay to demonstrate that HHV‐6A infection of T lymphocytes enables cell–cell fusion of these cells to astrocytes or to oligodendroglial cells. This fusion is mediated by the interaction between viral glycoproteins expressed on the membrane of the infected cells and CD46 on the glial targets, and is also observed using cells expressing recombinant MV glycoproteins. These data suggest a mechanism that involves cell–cell fusion by which certain viruses could spread the infection from the periphery to the cells in the nervous system. 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Published 2005 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Astrocytes - immunology</subject><subject>Brain - immunology</subject><subject>Brain - virology</subject><subject>Capsid Proteins - immunology</subject><subject>cell fusion</subject><subject>Central Nervous System Viral Diseases - immunology</subject><subject>Herpesvirus</subject><subject>Herpesvirus 6, Human - immunology</subject><subject>HHV-6</subject><subject>Humans</subject><subject>MCP</subject><subject>Measles virus</subject><subject>Membrane Cofactor Protein - immunology</subject><subject>Membrane Cofactor Protein - physiology</subject><subject>Membrane Fusion - immunology</subject><subject>Membrane Glycoproteins - immunology</subject><subject>Membrane Proteins - immunology</subject><subject>Mice</subject><subject>multiple sclerosis</subject><subject>Neuroglia - immunology</subject><subject>NIH 3T3 Cells</subject><subject>oligodendrocyte</subject><subject>Oligodendroglia - immunology</subject><subject>T-Lymphocytes - immunology</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9PwyAYh4nR6Jxe_ACmJw8mnfxpoRx16lxc5mXGI6H0rUG7dkKn7ttLt6k3PQAhPO_DLz-ETggeEIzpxXNl9YBiSuQO6hEss5gQxndRD2cyiUkiyQE69P4FYxIuYh8dkFRSLBjrITW8TnjU1FEnqSIDVeUjo-uoXNamteFB-0hHDgws2sZFZVjv1gX0uVqZZuGaFmwdz6GwuoViLYi7LQh8GD9Ce6WuPBxvzz56vL2ZDe_iycNoPLycxCaRmYyFoLjQtAQuICc01aQsSsaYkIynMhNCAs6ynBuQSZKG-HmRMFpwg3MBWlLWR2cbb0j0tgTfqrn1XQ5dQ7P0imc8Zan4HyQifEpTFsDzDWhc472DUi2cnWu3UgSrrnfVVabWvQf4dGtd5qGLX3RbdADIBviwFaz-UKnRZHz5LY03M9a38Pkzo92r4iFlqp6mI3V1fydmdHStpuwLY1SbeA</recordid><startdate>20051115</startdate><enddate>20051115</enddate><creator>Cassiani-Ingoni, Riccardo</creator><creator>Greenstone, Heather L.</creator><creator>Donati, Donatella</creator><creator>Fogdell-Hahn, Anna</creator><creator>Martinelli, Elena</creator><creator>Refai, Daniel</creator><creator>Martin, Roland</creator><creator>Berger, Edward A.</creator><creator>Jacobson, Steven</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20051115</creationdate><title>CD46 on glial cells can function as a receptor for viral glycoprotein-mediated cell-cell fusion</title><author>Cassiani-Ingoni, Riccardo ; 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While it is clear that oligodendrocytes and astrocytes are cell types commonly infected by these viruses, it is unclear whether oligodendrocytes express CD46, or which are the cellular mechanisms underlying the infection. We show that adult oligodendrocytes, as well as astrocytes and microglial cells, express CD46 on the cellular surface. Moreover, we employed a quantitative fusion assay to demonstrate that HHV‐6A infection of T lymphocytes enables cell–cell fusion of these cells to astrocytes or to oligodendroglial cells. This fusion is mediated by the interaction between viral glycoproteins expressed on the membrane of the infected cells and CD46 on the glial targets, and is also observed using cells expressing recombinant MV glycoproteins. These data suggest a mechanism that involves cell–cell fusion by which certain viruses could spread the infection from the periphery to the cells in the nervous system. 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subjects | Animals Astrocytes - immunology Brain - immunology Brain - virology Capsid Proteins - immunology cell fusion Central Nervous System Viral Diseases - immunology Herpesvirus Herpesvirus 6, Human - immunology HHV-6 Humans MCP Measles virus Membrane Cofactor Protein - immunology Membrane Cofactor Protein - physiology Membrane Fusion - immunology Membrane Glycoproteins - immunology Membrane Proteins - immunology Mice multiple sclerosis Neuroglia - immunology NIH 3T3 Cells oligodendrocyte Oligodendroglia - immunology T-Lymphocytes - immunology |
title | CD46 on glial cells can function as a receptor for viral glycoprotein-mediated cell-cell fusion |
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