Herpes simplex virus type 1 infection of mouse astrocytes treated with basic fibroblast growth factor
1 Department of Ophthalmology 2 Department of Microbiology and Immunology 3 Department of Neurology and 4 Physiology and Biophysics, P.O. Box 016880, Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Florida 33101, U.S.A. We explored a possible role for the basic fibroblast...
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Veröffentlicht in: | Journal of general virology 1992-07, Vol.73 (7), p.1845-1848 |
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creator | Dix, Richard D Hurst, Lisa Keane, Robert W |
description | 1 Department of Ophthalmology
2 Department of Microbiology and Immunology
3 Department of Neurology
and 4 Physiology and Biophysics, P.O. Box 016880, Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Florida 33101, U.S.A.
We explored a possible role for the basic fibroblast growth factor (FGF) receptor during herpes simplex virus type 1 (HSV-1) infection of primary mouse astrocytes, glial cells of the central nervous system known to express FGF receptors. Plaque reduction experiments showed that treatment of astrocyte monolayers with human recombinant basic FGF failed to inhibit HSV-1 infectivity, although treatment with either heparin or poly- L -lysine reduced it by approximately 100%. Identical results were obtained when monolayers of human embryonic lung fibroblasts or African green monkey kidney cells were treated with FGF, heparin or poly- L -lysine prior to HSV-1 infection. We conclude that the basic FGF receptor is not involved in the uptake of HSV-1 during productive infection of astrocytes. Our findings suggest that this molecule is not the predominant cellular receptor for HSV-1 among vertebrate cells and plays no role in defining HSV-1 neurotropism in vivo .
Received 29 January 1992;
accepted 17 March 1992. |
doi_str_mv | 10.1099/0022-1317-73-7-1845 |
format | Article |
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2 Department of Microbiology and Immunology
3 Department of Neurology
and 4 Physiology and Biophysics, P.O. Box 016880, Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Florida 33101, U.S.A.
We explored a possible role for the basic fibroblast growth factor (FGF) receptor during herpes simplex virus type 1 (HSV-1) infection of primary mouse astrocytes, glial cells of the central nervous system known to express FGF receptors. Plaque reduction experiments showed that treatment of astrocyte monolayers with human recombinant basic FGF failed to inhibit HSV-1 infectivity, although treatment with either heparin or poly- L -lysine reduced it by approximately 100%. Identical results were obtained when monolayers of human embryonic lung fibroblasts or African green monkey kidney cells were treated with FGF, heparin or poly- L -lysine prior to HSV-1 infection. We conclude that the basic FGF receptor is not involved in the uptake of HSV-1 during productive infection of astrocytes. Our findings suggest that this molecule is not the predominant cellular receptor for HSV-1 among vertebrate cells and plays no role in defining HSV-1 neurotropism in vivo .
Received 29 January 1992;
accepted 17 March 1992.</description><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/0022-1317-73-7-1845</identifier><identifier>PMID: 1321218</identifier><identifier>CODEN: JGVIAY</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>Animals ; Astrocytes - microbiology ; Biological and medical sciences ; Cells, Cultured ; Fibroblast Growth Factor 2 - pharmacology ; Fundamental and applied biological sciences. Psychology ; herpes simplex virus 1 ; Mice ; Mice, Inbred BALB C ; Microbiology ; Receptors, Cell Surface - physiology ; Receptors, Fibroblast Growth Factor ; Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains ; Simplexvirus - growth & development ; Virology</subject><ispartof>Journal of general virology, 1992-07, Vol.73 (7), p.1845-1848</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-9a8fb7a1f27ae6c5e118c297c346ad9360c00dd31c0b9d145f9e40d4a72dd2bb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3746,3747,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5441562$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1321218$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dix, Richard D</creatorcontrib><creatorcontrib>Hurst, Lisa</creatorcontrib><creatorcontrib>Keane, Robert W</creatorcontrib><title>Herpes simplex virus type 1 infection of mouse astrocytes treated with basic fibroblast growth factor</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>1 Department of Ophthalmology
2 Department of Microbiology and Immunology
3 Department of Neurology
and 4 Physiology and Biophysics, P.O. Box 016880, Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Florida 33101, U.S.A.
We explored a possible role for the basic fibroblast growth factor (FGF) receptor during herpes simplex virus type 1 (HSV-1) infection of primary mouse astrocytes, glial cells of the central nervous system known to express FGF receptors. Plaque reduction experiments showed that treatment of astrocyte monolayers with human recombinant basic FGF failed to inhibit HSV-1 infectivity, although treatment with either heparin or poly- L -lysine reduced it by approximately 100%. Identical results were obtained when monolayers of human embryonic lung fibroblasts or African green monkey kidney cells were treated with FGF, heparin or poly- L -lysine prior to HSV-1 infection. We conclude that the basic FGF receptor is not involved in the uptake of HSV-1 during productive infection of astrocytes. Our findings suggest that this molecule is not the predominant cellular receptor for HSV-1 among vertebrate cells and plays no role in defining HSV-1 neurotropism in vivo .
Received 29 January 1992;
accepted 17 March 1992.</description><subject>Animals</subject><subject>Astrocytes - microbiology</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Fibroblast Growth Factor 2 - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>herpes simplex virus 1</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbiology</subject><subject>Receptors, Cell Surface - physiology</subject><subject>Receptors, Fibroblast Growth Factor</subject><subject>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</subject><subject>Simplexvirus - growth & development</subject><subject>Virology</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUGLFDEQhYMo6-zqLxAhBxEvrakknXQfZVFXWPCi55BOV2Yi3Z02yTjOvzfDDLvHPQXqfe-leEXIG2AfgfX9J8Y4b0CAbrRodAOdbJ-RDUjVNrzqz8nmgXhJrnP-zRhI2eorcgWCA4duQ_AO04qZ5jCvE_6jf0PaZ1qOK1KgYfHoSogLjZ7OcZ-R2lxSdMdSLSWhLTjSQyg7OtgcHPVhSHGYKkS3KR7q3FtXYnpFXng7ZXx9eW_Ir69fft7eNfc_vn2__XzfOCm60vS284O24Lm2qFyLAJ3jvXZCKjv2QjHH2DgKcGzoR5Ct71GyUVrNx5EPg7gh78-5a4p_9piLmUN2OE12wbq-0YIp6Lh-EgSletV1qoLiDLoUc07ozZrCbNPRADOnK5hTx-bUcU032pyuUF1vL_H7Ycbx0XOuvervLrrNzk4-2cWF_IC1UkKreMU-nLFd2O4OIaHZ4jKHusoQoqmnevzxP6vpnrg</recordid><startdate>19920701</startdate><enddate>19920701</enddate><creator>Dix, Richard D</creator><creator>Hurst, Lisa</creator><creator>Keane, Robert W</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</general><scope>IQODW</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>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19920701</creationdate><title>Herpes simplex virus type 1 infection of mouse astrocytes treated with basic fibroblast growth factor</title><author>Dix, Richard D ; Hurst, Lisa ; Keane, Robert W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-9a8fb7a1f27ae6c5e118c297c346ad9360c00dd31c0b9d145f9e40d4a72dd2bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animals</topic><topic>Astrocytes - microbiology</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Fibroblast Growth Factor 2 - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>herpes simplex virus 1</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbiology</topic><topic>Receptors, Cell Surface - physiology</topic><topic>Receptors, Fibroblast Growth Factor</topic><topic>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</topic><topic>Simplexvirus - growth & development</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dix, Richard D</creatorcontrib><creatorcontrib>Hurst, Lisa</creatorcontrib><creatorcontrib>Keane, Robert W</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dix, Richard D</au><au>Hurst, Lisa</au><au>Keane, Robert W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Herpes simplex virus type 1 infection of mouse astrocytes treated with basic fibroblast growth factor</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>1992-07-01</date><risdate>1992</risdate><volume>73</volume><issue>7</issue><spage>1845</spage><epage>1848</epage><pages>1845-1848</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><coden>JGVIAY</coden><abstract>1 Department of Ophthalmology
2 Department of Microbiology and Immunology
3 Department of Neurology
and 4 Physiology and Biophysics, P.O. Box 016880, Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Florida 33101, U.S.A.
We explored a possible role for the basic fibroblast growth factor (FGF) receptor during herpes simplex virus type 1 (HSV-1) infection of primary mouse astrocytes, glial cells of the central nervous system known to express FGF receptors. Plaque reduction experiments showed that treatment of astrocyte monolayers with human recombinant basic FGF failed to inhibit HSV-1 infectivity, although treatment with either heparin or poly- L -lysine reduced it by approximately 100%. Identical results were obtained when monolayers of human embryonic lung fibroblasts or African green monkey kidney cells were treated with FGF, heparin or poly- L -lysine prior to HSV-1 infection. We conclude that the basic FGF receptor is not involved in the uptake of HSV-1 during productive infection of astrocytes. Our findings suggest that this molecule is not the predominant cellular receptor for HSV-1 among vertebrate cells and plays no role in defining HSV-1 neurotropism in vivo .
Received 29 January 1992;
accepted 17 March 1992.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>1321218</pmid><doi>10.1099/0022-1317-73-7-1845</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Microbiology Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Astrocytes - microbiology Biological and medical sciences Cells, Cultured Fibroblast Growth Factor 2 - pharmacology Fundamental and applied biological sciences. Psychology herpes simplex virus 1 Mice Mice, Inbred BALB C Microbiology Receptors, Cell Surface - physiology Receptors, Fibroblast Growth Factor Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains Simplexvirus - growth & development Virology |
title | Herpes simplex virus type 1 infection of mouse astrocytes treated with basic fibroblast growth factor |
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