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Mice deficient in PKC theta demonstrate impaired in vivo T cell activation and protection from T cell-mediated inflammatory diseases
In the present study we have characterized T cell-driven immune function in mice that are genetically deficient in PKC theta. In response to simple immunologic stimulation invoked by in vivo T cell receptor (TCR) cross-linking, these mice showed significantly depressed plasma cytokine levels for IL-...
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Published in: | Autoimmunity (Chur, Switzerland) Switzerland), 2006-09, Vol.39 (6), p.469-478 |
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container_title | Autoimmunity (Chur, Switzerland) |
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creator | Anderson, Karen Fitzgerald, Michael DuPont, Michelle Wang, Tao Paz, Nancy Dorsch, Marion Healy, Aileen Xu, Yajun Ocain, Tim Schopf, Lisa Jaffee, Bruce Picarella, Dominic |
description | In the present study we have characterized T cell-driven immune function in mice that are genetically deficient in PKC theta. In response to simple immunologic stimulation invoked by in vivo T cell receptor (TCR) cross-linking, these mice showed significantly depressed plasma cytokine levels for IL-2, IL-4, IFNγ, and TNFα compared to wild-type (WT) mice. In parallel, spleen mRNA levels for these cytokines were reduced, and NF-κB activation was also reduced in PKC theta knockouts (KO). Injection of allogeneic cells into the footpad of PKC theta deficient mice provoked a significantly diminished local T cell response compared to WT mice similarly challenged. Unlike comparable cells from wild type mice, CD45RBhi T cells harvested from PKC theta deficient mice failed to induce colitis in the SCID-CD45RB cell transfer model of IBD. In another T cell-dependent model of inflammatory disease, PKC theta deficient animals developed far less severe neurologic signs and reduced spinal cord inflammatory cell infiltrate compared to WT controls in the MOG-induced EAE model. A fundamental role for PKC theta in T cell activation and in the development of T cell-mediated inflammatory diseases is indicated by these results. |
doi_str_mv | 10.1080/08916930600907954 |
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In response to simple immunologic stimulation invoked by in vivo T cell receptor (TCR) cross-linking, these mice showed significantly depressed plasma cytokine levels for IL-2, IL-4, IFNγ, and TNFα compared to wild-type (WT) mice. In parallel, spleen mRNA levels for these cytokines were reduced, and NF-κB activation was also reduced in PKC theta knockouts (KO). Injection of allogeneic cells into the footpad of PKC theta deficient mice provoked a significantly diminished local T cell response compared to WT mice similarly challenged. Unlike comparable cells from wild type mice, CD45RBhi T cells harvested from PKC theta deficient mice failed to induce colitis in the SCID-CD45RB cell transfer model of IBD. In another T cell-dependent model of inflammatory disease, PKC theta deficient animals developed far less severe neurologic signs and reduced spinal cord inflammatory cell infiltrate compared to WT controls in the MOG-induced EAE model. A fundamental role for PKC theta in T cell activation and in the development of T cell-mediated inflammatory diseases is indicated by these results.</description><identifier>ISSN: 0891-6934</identifier><identifier>EISSN: 1607-842X</identifier><identifier>DOI: 10.1080/08916930600907954</identifier><identifier>PMID: 17060026</identifier><language>eng</language><publisher>Abingdon: Informa UK Ltd</publisher><subject>Animals ; autoimmune disease ; Biological and medical sciences ; CD4 Antigens - immunology ; Cell Proliferation ; Cytokines - blood ; Cytokines - metabolism ; Disease Models, Animal ; EAE ; Encephalomyelitis, Autoimmune, Experimental - immunology ; Encephalomyelitis, Autoimmune, Experimental - pathology ; Enzyme Activation ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; General aspects ; IBD ; Immunopathology ; Inflammation - immunology ; Inflammation - pathology ; Inflammatory Bowel Diseases - immunology ; Inflammatory Bowel Diseases - pathology ; Isoenzymes - genetics ; Isoenzymes - immunology ; Leukocyte Common Antigens - immunology ; Lymph Nodes - immunology ; Lymph Nodes - pathology ; Lymphocyte Activation ; Medical sciences ; Mice ; Mice, Knockout ; Mice, SCID ; NF-kappa B - metabolism ; PKC theta ; Protein Kinase C - genetics ; Protein Kinase C - immunology ; Protein Kinase C-theta ; Receptors, Antigen, T-Cell - immunology ; RNA, Messenger - blood ; RNA, Messenger - metabolism ; Spinal Cord - immunology ; Spinal Cord - pathology ; Spleen - metabolism ; T cell activation</subject><ispartof>Autoimmunity (Chur, Switzerland), 2006-09, Vol.39 (6), p.469-478</ispartof><rights>2006 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2006</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-5a490533ca8883923bda5cf34ea7fb27f2139b9c817ae31216bd8dd7b3a813273</citedby><cites>FETCH-LOGICAL-c465t-5a490533ca8883923bda5cf34ea7fb27f2139b9c817ae31216bd8dd7b3a813273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18251725$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17060026$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anderson, Karen</creatorcontrib><creatorcontrib>Fitzgerald, Michael</creatorcontrib><creatorcontrib>DuPont, Michelle</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Paz, Nancy</creatorcontrib><creatorcontrib>Dorsch, Marion</creatorcontrib><creatorcontrib>Healy, Aileen</creatorcontrib><creatorcontrib>Xu, Yajun</creatorcontrib><creatorcontrib>Ocain, Tim</creatorcontrib><creatorcontrib>Schopf, Lisa</creatorcontrib><creatorcontrib>Jaffee, Bruce</creatorcontrib><creatorcontrib>Picarella, Dominic</creatorcontrib><title>Mice deficient in PKC theta demonstrate impaired in vivo T cell activation and protection from T cell-mediated inflammatory diseases</title><title>Autoimmunity (Chur, Switzerland)</title><addtitle>Autoimmunity</addtitle><description>In the present study we have characterized T cell-driven immune function in mice that are genetically deficient in PKC theta. In response to simple immunologic stimulation invoked by in vivo T cell receptor (TCR) cross-linking, these mice showed significantly depressed plasma cytokine levels for IL-2, IL-4, IFNγ, and TNFα compared to wild-type (WT) mice. In parallel, spleen mRNA levels for these cytokines were reduced, and NF-κB activation was also reduced in PKC theta knockouts (KO). Injection of allogeneic cells into the footpad of PKC theta deficient mice provoked a significantly diminished local T cell response compared to WT mice similarly challenged. Unlike comparable cells from wild type mice, CD45RBhi T cells harvested from PKC theta deficient mice failed to induce colitis in the SCID-CD45RB cell transfer model of IBD. In another T cell-dependent model of inflammatory disease, PKC theta deficient animals developed far less severe neurologic signs and reduced spinal cord inflammatory cell infiltrate compared to WT controls in the MOG-induced EAE model. A fundamental role for PKC theta in T cell activation and in the development of T cell-mediated inflammatory diseases is indicated by these results.</description><subject>Animals</subject><subject>autoimmune disease</subject><subject>Biological and medical sciences</subject><subject>CD4 Antigens - immunology</subject><subject>Cell Proliferation</subject><subject>Cytokines - blood</subject><subject>Cytokines - metabolism</subject><subject>Disease Models, Animal</subject><subject>EAE</subject><subject>Encephalomyelitis, Autoimmune, Experimental - immunology</subject><subject>Encephalomyelitis, Autoimmune, Experimental - pathology</subject><subject>Enzyme Activation</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>General aspects</subject><subject>IBD</subject><subject>Immunopathology</subject><subject>Inflammation - immunology</subject><subject>Inflammation - pathology</subject><subject>Inflammatory Bowel Diseases - immunology</subject><subject>Inflammatory Bowel Diseases - pathology</subject><subject>Isoenzymes - genetics</subject><subject>Isoenzymes - immunology</subject><subject>Leukocyte Common Antigens - immunology</subject><subject>Lymph Nodes - immunology</subject><subject>Lymph Nodes - pathology</subject><subject>Lymphocyte Activation</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Mice, SCID</subject><subject>NF-kappa B - metabolism</subject><subject>PKC theta</subject><subject>Protein Kinase C - genetics</subject><subject>Protein Kinase C - immunology</subject><subject>Protein Kinase C-theta</subject><subject>Receptors, Antigen, T-Cell - immunology</subject><subject>RNA, Messenger - blood</subject><subject>RNA, Messenger - metabolism</subject><subject>Spinal Cord - immunology</subject><subject>Spinal Cord - pathology</subject><subject>Spleen - metabolism</subject><subject>T cell activation</subject><issn>0891-6934</issn><issn>1607-842X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkUuLFDEUhYMoTtv6A9xINrorzaOqkqAbaXzhiC5GcFfcSm7RGaoqbZJu6b0_3JTdMogwrkKS7xzOvYeQx5w950yzF0wb3hrJWsYMU6ap75AVb5mqdC2-3SWr5b8qQH1BHqR0zRgTqq3vkwuuFo1oV-TnJ2-ROhy89Thn6mf65eOG5i1mKM9TmFOOkJH6aQc-oluIgz8EekUtjiMFm_0Bsg8zhdnRXQwZ7e_rEMN0pqoJnS8ui3oYYZogh3ikzieEhOkhuTfAmPDR-VyTr2_fXG3eV5ef333YvL6sbN02uWqgNqyR0oLWWhoheweNHWSNoIZeqEFwaXpjNVeAkgve9k47p3oJmkuh5Jo8O_mWlN_3mHI3-bTkgxnDPnWtNlo2df1fkBupWVtM14SfQBtDShGHbhf9BPHYcdYtHXX_dFQ0T87m-77s5UZxLqUAT88AJAvjEGG2Pt1wWjRciaZwr05cWWqIE_wIcXRdhuMY4h-RvC3Hy7_kW4Qxby1E7K7DPs6liVum-AUKz7-k</recordid><startdate>20060901</startdate><enddate>20060901</enddate><creator>Anderson, Karen</creator><creator>Fitzgerald, Michael</creator><creator>DuPont, Michelle</creator><creator>Wang, Tao</creator><creator>Paz, Nancy</creator><creator>Dorsch, Marion</creator><creator>Healy, Aileen</creator><creator>Xu, Yajun</creator><creator>Ocain, Tim</creator><creator>Schopf, Lisa</creator><creator>Jaffee, Bruce</creator><creator>Picarella, Dominic</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Taylor and Francis</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20060901</creationdate><title>Mice deficient in PKC theta demonstrate impaired in vivo T cell activation and protection from T cell-mediated inflammatory diseases</title><author>Anderson, Karen ; Fitzgerald, Michael ; DuPont, Michelle ; Wang, Tao ; Paz, Nancy ; Dorsch, Marion ; Healy, Aileen ; Xu, Yajun ; Ocain, Tim ; Schopf, Lisa ; Jaffee, Bruce ; Picarella, Dominic</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-5a490533ca8883923bda5cf34ea7fb27f2139b9c817ae31216bd8dd7b3a813273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>autoimmune disease</topic><topic>Biological and medical sciences</topic><topic>CD4 Antigens - immunology</topic><topic>Cell Proliferation</topic><topic>Cytokines - blood</topic><topic>Cytokines - metabolism</topic><topic>Disease Models, Animal</topic><topic>EAE</topic><topic>Encephalomyelitis, Autoimmune, Experimental - immunology</topic><topic>Encephalomyelitis, Autoimmune, Experimental - pathology</topic><topic>Enzyme Activation</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>General aspects</topic><topic>IBD</topic><topic>Immunopathology</topic><topic>Inflammation - immunology</topic><topic>Inflammation - pathology</topic><topic>Inflammatory Bowel Diseases - immunology</topic><topic>Inflammatory Bowel Diseases - pathology</topic><topic>Isoenzymes - genetics</topic><topic>Isoenzymes - immunology</topic><topic>Leukocyte Common Antigens - immunology</topic><topic>Lymph Nodes - immunology</topic><topic>Lymph Nodes - pathology</topic><topic>Lymphocyte Activation</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Mice, SCID</topic><topic>NF-kappa B - metabolism</topic><topic>PKC theta</topic><topic>Protein Kinase C - genetics</topic><topic>Protein Kinase C - immunology</topic><topic>Protein Kinase C-theta</topic><topic>Receptors, Antigen, T-Cell - immunology</topic><topic>RNA, Messenger - blood</topic><topic>RNA, Messenger - metabolism</topic><topic>Spinal Cord - immunology</topic><topic>Spinal Cord - pathology</topic><topic>Spleen - metabolism</topic><topic>T cell activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anderson, Karen</creatorcontrib><creatorcontrib>Fitzgerald, Michael</creatorcontrib><creatorcontrib>DuPont, Michelle</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Paz, Nancy</creatorcontrib><creatorcontrib>Dorsch, Marion</creatorcontrib><creatorcontrib>Healy, Aileen</creatorcontrib><creatorcontrib>Xu, Yajun</creatorcontrib><creatorcontrib>Ocain, Tim</creatorcontrib><creatorcontrib>Schopf, Lisa</creatorcontrib><creatorcontrib>Jaffee, Bruce</creatorcontrib><creatorcontrib>Picarella, Dominic</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Autoimmunity (Chur, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anderson, Karen</au><au>Fitzgerald, Michael</au><au>DuPont, Michelle</au><au>Wang, Tao</au><au>Paz, Nancy</au><au>Dorsch, Marion</au><au>Healy, Aileen</au><au>Xu, Yajun</au><au>Ocain, Tim</au><au>Schopf, Lisa</au><au>Jaffee, Bruce</au><au>Picarella, Dominic</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mice deficient in PKC theta demonstrate impaired in vivo T cell activation and protection from T cell-mediated inflammatory diseases</atitle><jtitle>Autoimmunity (Chur, Switzerland)</jtitle><addtitle>Autoimmunity</addtitle><date>2006-09-01</date><risdate>2006</risdate><volume>39</volume><issue>6</issue><spage>469</spage><epage>478</epage><pages>469-478</pages><issn>0891-6934</issn><eissn>1607-842X</eissn><abstract>In the present study we have characterized T cell-driven immune function in mice that are genetically deficient in PKC theta. In response to simple immunologic stimulation invoked by in vivo T cell receptor (TCR) cross-linking, these mice showed significantly depressed plasma cytokine levels for IL-2, IL-4, IFNγ, and TNFα compared to wild-type (WT) mice. In parallel, spleen mRNA levels for these cytokines were reduced, and NF-κB activation was also reduced in PKC theta knockouts (KO). Injection of allogeneic cells into the footpad of PKC theta deficient mice provoked a significantly diminished local T cell response compared to WT mice similarly challenged. Unlike comparable cells from wild type mice, CD45RBhi T cells harvested from PKC theta deficient mice failed to induce colitis in the SCID-CD45RB cell transfer model of IBD. In another T cell-dependent model of inflammatory disease, PKC theta deficient animals developed far less severe neurologic signs and reduced spinal cord inflammatory cell infiltrate compared to WT controls in the MOG-induced EAE model. A fundamental role for PKC theta in T cell activation and in the development of T cell-mediated inflammatory diseases is indicated by these results.</abstract><cop>Abingdon</cop><pub>Informa UK Ltd</pub><pmid>17060026</pmid><doi>10.1080/08916930600907954</doi><tpages>10</tpages></addata></record> |
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subjects | Animals autoimmune disease Biological and medical sciences CD4 Antigens - immunology Cell Proliferation Cytokines - blood Cytokines - metabolism Disease Models, Animal EAE Encephalomyelitis, Autoimmune, Experimental - immunology Encephalomyelitis, Autoimmune, Experimental - pathology Enzyme Activation Female Fundamental and applied biological sciences. Psychology Fundamental immunology General aspects IBD Immunopathology Inflammation - immunology Inflammation - pathology Inflammatory Bowel Diseases - immunology Inflammatory Bowel Diseases - pathology Isoenzymes - genetics Isoenzymes - immunology Leukocyte Common Antigens - immunology Lymph Nodes - immunology Lymph Nodes - pathology Lymphocyte Activation Medical sciences Mice Mice, Knockout Mice, SCID NF-kappa B - metabolism PKC theta Protein Kinase C - genetics Protein Kinase C - immunology Protein Kinase C-theta Receptors, Antigen, T-Cell - immunology RNA, Messenger - blood RNA, Messenger - metabolism Spinal Cord - immunology Spinal Cord - pathology Spleen - metabolism T cell activation |
title | Mice deficient in PKC theta demonstrate impaired in vivo T cell activation and protection from T cell-mediated inflammatory diseases |
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