HIV Nef Inhibits T Cell Migration
Nef is a viral regulatory protein of the human immunodeficiency virus (HIV) that has been shown to contribute to disease progression. Among its putative effects on T cell functions are the down-regulation of CD4 and major histocompatibility class I surface molecules. These effects occur in part via...
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Veröffentlicht in: | The Journal of biological chemistry 2002-11, Vol.277 (48), p.46079-46084 |
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container_issue | 48 |
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container_title | The Journal of biological chemistry |
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creator | Choe, Evangeline Y Schoenberger, Elena S Groopman, Jerome E Park, In-Woo |
description | Nef is a viral regulatory protein of the human immunodeficiency virus (HIV) that has been shown to contribute to disease progression.
Among its putative effects on T cell functions are the down-regulation of CD4 and major histocompatibility class I surface
molecules. These effects occur in part via Nef interactions with intracellular signaling molecules. We sought to better characterize
the effects of HIV Nef on T cell function by examining chemotaxis in response to stromal cell-derived factor-1α (SDF-1α) as
well as CXCR4 signaling molecules. Here, we report the novel observation that HIV Nef inhibited chemotaxis in response to
SDF-1α in both Jurkat T cells and primary peripheral CD4+ T lymphocytes. Our data indicate that HIV Nef altered critical downstream
molecules in the CXCR4 pathway, including focal adhesion kinases. These findings suggest that HIV Nef may blunt the T cell
response to chemokines. Because T lymphocyte migration is an integral component of host defense, HIV Nef may thereby contribute
to the pathogenesis of AIDS. |
doi_str_mv | 10.1074/jbc.M204698200 |
format | Article |
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Among its putative effects on T cell functions are the down-regulation of CD4 and major histocompatibility class I surface
molecules. These effects occur in part via Nef interactions with intracellular signaling molecules. We sought to better characterize
the effects of HIV Nef on T cell function by examining chemotaxis in response to stromal cell-derived factor-1α (SDF-1α) as
well as CXCR4 signaling molecules. Here, we report the novel observation that HIV Nef inhibited chemotaxis in response to
SDF-1α in both Jurkat T cells and primary peripheral CD4+ T lymphocytes. Our data indicate that HIV Nef altered critical downstream
molecules in the CXCR4 pathway, including focal adhesion kinases. These findings suggest that HIV Nef may blunt the T cell
response to chemokines. Because T lymphocyte migration is an integral component of host defense, HIV Nef may thereby contribute
to the pathogenesis of AIDS.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M204698200</identifier><identifier>PMID: 12354773</identifier><language>eng</language><publisher>United States: American Society for Biochemistry and Molecular Biology</publisher><subject>CD4-Positive T-Lymphocytes - cytology ; Cell Movement ; Chemokine CXCL12 ; Chemokines, CXC - physiology ; Gene Products, nef - metabolism ; Gene Products, nef - physiology ; Green Fluorescent Proteins ; Humans ; Jurkat Cells ; Luminescent Proteins - metabolism ; Recombinant Fusion Proteins - metabolism ; Signal Transduction</subject><ispartof>The Journal of biological chemistry, 2002-11, Vol.277 (48), p.46079-46084</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-353785651e13b5e9297b074a1d26526a939c93c84c02e3d0e10a26eb0ee8df4b3</citedby><cites>FETCH-LOGICAL-c391t-353785651e13b5e9297b074a1d26526a939c93c84c02e3d0e10a26eb0ee8df4b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12354773$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choe, Evangeline Y</creatorcontrib><creatorcontrib>Schoenberger, Elena S</creatorcontrib><creatorcontrib>Groopman, Jerome E</creatorcontrib><creatorcontrib>Park, In-Woo</creatorcontrib><title>HIV Nef Inhibits T Cell Migration</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Nef is a viral regulatory protein of the human immunodeficiency virus (HIV) that has been shown to contribute to disease progression.
Among its putative effects on T cell functions are the down-regulation of CD4 and major histocompatibility class I surface
molecules. These effects occur in part via Nef interactions with intracellular signaling molecules. We sought to better characterize
the effects of HIV Nef on T cell function by examining chemotaxis in response to stromal cell-derived factor-1α (SDF-1α) as
well as CXCR4 signaling molecules. Here, we report the novel observation that HIV Nef inhibited chemotaxis in response to
SDF-1α in both Jurkat T cells and primary peripheral CD4+ T lymphocytes. Our data indicate that HIV Nef altered critical downstream
molecules in the CXCR4 pathway, including focal adhesion kinases. These findings suggest that HIV Nef may blunt the T cell
response to chemokines. Because T lymphocyte migration is an integral component of host defense, HIV Nef may thereby contribute
to the pathogenesis of AIDS.</description><subject>CD4-Positive T-Lymphocytes - cytology</subject><subject>Cell Movement</subject><subject>Chemokine CXCL12</subject><subject>Chemokines, CXC - physiology</subject><subject>Gene Products, nef - metabolism</subject><subject>Gene Products, nef - physiology</subject><subject>Green Fluorescent Proteins</subject><subject>Humans</subject><subject>Jurkat Cells</subject><subject>Luminescent Proteins - metabolism</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Signal Transduction</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PwkAQhjdGI4hePZqaGG_F2a_u7tEQFRLQCxpvm3Y7hSWUYrfE-O9dAwlH5zKXZ96ZeQi5pjCkoMTDqnDDGQORGc0ATkifguYpl_TzlPQBGE0Nk7pHLkJYQSxh6DnpUcalUIr3ye148pG8YpVMNktf-C4k82SE63Uy84s273yzuSRnVb4OeHXoA_L-_DQfjdPp28tk9DhNHTe0iyu50jKTFCkvJBpmVBEPzGnJMsmy3HDjDHdaOGDIS0AKOcuwAERdVqLgA3K_z922zdcOQ2drH1w8Jd9gswtWMcV0_PlfkGrJtRIQweEedG0TQouV3ba-ztsfS8H-2bPRnj3aiwM3h-RdUWN5xA-6InC3B5Z-sfz2LdrCN26JtWVKWaGtyEAZ_gvOQnLj</recordid><startdate>20021129</startdate><enddate>20021129</enddate><creator>Choe, Evangeline Y</creator><creator>Schoenberger, Elena S</creator><creator>Groopman, Jerome E</creator><creator>Park, In-Woo</creator><general>American Society for Biochemistry and Molecular Biology</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20021129</creationdate><title>HIV Nef Inhibits T Cell Migration</title><author>Choe, Evangeline Y ; Schoenberger, Elena S ; Groopman, Jerome E ; Park, In-Woo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-353785651e13b5e9297b074a1d26526a939c93c84c02e3d0e10a26eb0ee8df4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>CD4-Positive T-Lymphocytes - cytology</topic><topic>Cell Movement</topic><topic>Chemokine CXCL12</topic><topic>Chemokines, CXC - physiology</topic><topic>Gene Products, nef - metabolism</topic><topic>Gene Products, nef - physiology</topic><topic>Green Fluorescent Proteins</topic><topic>Humans</topic><topic>Jurkat Cells</topic><topic>Luminescent Proteins - metabolism</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choe, Evangeline Y</creatorcontrib><creatorcontrib>Schoenberger, Elena S</creatorcontrib><creatorcontrib>Groopman, Jerome E</creatorcontrib><creatorcontrib>Park, In-Woo</creatorcontrib><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>Virology and AIDS 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>Choe, Evangeline Y</au><au>Schoenberger, Elena S</au><au>Groopman, Jerome E</au><au>Park, In-Woo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HIV Nef Inhibits T Cell Migration</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2002-11-29</date><risdate>2002</risdate><volume>277</volume><issue>48</issue><spage>46079</spage><epage>46084</epage><pages>46079-46084</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Nef is a viral regulatory protein of the human immunodeficiency virus (HIV) that has been shown to contribute to disease progression.
Among its putative effects on T cell functions are the down-regulation of CD4 and major histocompatibility class I surface
molecules. These effects occur in part via Nef interactions with intracellular signaling molecules. We sought to better characterize
the effects of HIV Nef on T cell function by examining chemotaxis in response to stromal cell-derived factor-1α (SDF-1α) as
well as CXCR4 signaling molecules. Here, we report the novel observation that HIV Nef inhibited chemotaxis in response to
SDF-1α in both Jurkat T cells and primary peripheral CD4+ T lymphocytes. Our data indicate that HIV Nef altered critical downstream
molecules in the CXCR4 pathway, including focal adhesion kinases. These findings suggest that HIV Nef may blunt the T cell
response to chemokines. Because T lymphocyte migration is an integral component of host defense, HIV Nef may thereby contribute
to the pathogenesis of AIDS.</abstract><cop>United States</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>12354773</pmid><doi>10.1074/jbc.M204698200</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | CD4-Positive T-Lymphocytes - cytology Cell Movement Chemokine CXCL12 Chemokines, CXC - physiology Gene Products, nef - metabolism Gene Products, nef - physiology Green Fluorescent Proteins Humans Jurkat Cells Luminescent Proteins - metabolism Recombinant Fusion Proteins - metabolism Signal Transduction |
title | HIV Nef Inhibits T Cell Migration |
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