Loading…
E-Selectin, Thymus- and Activation-Regulated Chemokine/CCL17, and Intercellular Adhesion Molecule-1 Are Constitutively Coexpressed in Dermal Microvessels: A Foundation for a Cutaneous Immunosurveillance System
The success of the cutaneous immune system reflects its ability to rapidly and efficiently recruit leukocytes to areas of trauma and infection. Skin-homing memory T cells expressing cutaneous lymphocyte-associated Ag tether on the walls of postcapillary venules in inflamed skin via interaction with...
Saved in:
Published in: | The Journal of immunology (1950) 2004-02, Vol.172 (3), p.1575-1581 |
---|---|
Main Authors: | , , , |
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-c475t-b6634dd4bb45dd444b78f8b7870a22e7ed4fd3239586b2887610a7eea23fb4b43 |
---|---|
cites | cdi_FETCH-LOGICAL-c475t-b6634dd4bb45dd444b78f8b7870a22e7ed4fd3239586b2887610a7eea23fb4b43 |
container_end_page | 1581 |
container_issue | 3 |
container_start_page | 1575 |
container_title | The Journal of immunology (1950) |
container_volume | 172 |
creator | Chong, Benjamin F Murphy, Jo-Ellen Kupper, Thomas S Fuhlbrigge, Robert C |
description | The success of the cutaneous immune system reflects its ability to rapidly and efficiently recruit leukocytes to areas of trauma and infection. Skin-homing memory T cells expressing cutaneous lymphocyte-associated Ag tether on the walls of postcapillary venules in inflamed skin via interaction with endothelial E-selectin and roll in response to the shear stress imparted by flowing blood. Rolling cells sample the vascular surface for chemoattractant compounds (e.g., thymus- and activation-regulated chemokine/CCL17 interacting with CCR4 on the leukocyte surface) and, if successfully stimulated, progress to firm arrest and transmigration mediated by LFA-1 and vascular ICAM-1. Although it is established that this sequence of events draws T cells into inflamed skin, the mechanisms directing trafficking of T cells to noninflamed skin are less well characterized. We hypothesized that basal expression and colocalization of E-selectin, chemokine (e.g., CCL17), and ICAM-1 in dermal vessels could serve to recruit T cells to noninflamed human skin. Immunohistochemical staining for E-selectin and CD31 demonstrated E-selectin expression in a restricted subset of dermal vessels in noninflamed human skin from three different sites. Confocal multicolor immunofluorescence imaging revealed a nonuniform distribution of E-selectin in dermal vessels as well as colocalization of E-selectin with CCL17 and ICAM-1. Coexpression of these molecules on blood vessels in noninflamed skin provides the basis for a model of cutaneous immunosurveillance system active in the absence of pathologic inflammation. |
doi_str_mv | 10.4049/jimmunol.172.3.1575 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_80116531</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19232508</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-b6634dd4bb45dd444b78f8b7870a22e7ed4fd3239586b2887610a7eea23fb4b43</originalsourceid><addsrcrecordid>eNqFkd1u1DAQhSMEokvhCZCQr-Cm2fovcZa7KLSw0lZItFxbTjJpXBxna8e77GP2jer9QXCHZHnk0TdH43OS5D3Bc4754vJBD0Owo5kTQedsTjKRvUhmJMtwmuc4f5nMMKY0JSIXZ8kb7x8wxjmm_HVyRrhg8YhZ8nSV3oKBZtL2At31uyH4FCnbojK2NmrSo01_wH0waoIWVT0M4y9t4bKqVkRcHMilncA1YEyEHCrbHnycQjdjlA0GUoJKB6garZ_0FKIqmF18wu-1A--jqrboC7hBGXSjGzdu9l3jP6MSXY_BtoclUDc6pFAVJmVhDB4tD5_3wW1AG6NsA-h25ycY3iavOmU8vDvV8-Tn9dVd9S1dff-6rMpV2nCRTWmd54y3La9rnsXCeS2KroiXwIpSENDyrmWULbIir2lRiJxgJQAUZV3Na87Ok49H3bUbHwP4SQ7a7204LigLTEieMfJfkCwooxkuIsiOYDTBewedXDs9KLeTBMt95PJP5DJGLpncRx6nPpzkQz1A-3fmlHEEPh2BXt_3W-1A-ui1iTiR2-32H6lnC6-7bA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19232508</pqid></control><display><type>article</type><title>E-Selectin, Thymus- and Activation-Regulated Chemokine/CCL17, and Intercellular Adhesion Molecule-1 Are Constitutively Coexpressed in Dermal Microvessels: A Foundation for a Cutaneous Immunosurveillance System</title><source>EZB Electronic Journals Library</source><creator>Chong, Benjamin F ; Murphy, Jo-Ellen ; Kupper, Thomas S ; Fuhlbrigge, Robert C</creator><creatorcontrib>Chong, Benjamin F ; Murphy, Jo-Ellen ; Kupper, Thomas S ; Fuhlbrigge, Robert C</creatorcontrib><description>The success of the cutaneous immune system reflects its ability to rapidly and efficiently recruit leukocytes to areas of trauma and infection. Skin-homing memory T cells expressing cutaneous lymphocyte-associated Ag tether on the walls of postcapillary venules in inflamed skin via interaction with endothelial E-selectin and roll in response to the shear stress imparted by flowing blood. Rolling cells sample the vascular surface for chemoattractant compounds (e.g., thymus- and activation-regulated chemokine/CCL17 interacting with CCR4 on the leukocyte surface) and, if successfully stimulated, progress to firm arrest and transmigration mediated by LFA-1 and vascular ICAM-1. Although it is established that this sequence of events draws T cells into inflamed skin, the mechanisms directing trafficking of T cells to noninflamed skin are less well characterized. We hypothesized that basal expression and colocalization of E-selectin, chemokine (e.g., CCL17), and ICAM-1 in dermal vessels could serve to recruit T cells to noninflamed human skin. Immunohistochemical staining for E-selectin and CD31 demonstrated E-selectin expression in a restricted subset of dermal vessels in noninflamed human skin from three different sites. Confocal multicolor immunofluorescence imaging revealed a nonuniform distribution of E-selectin in dermal vessels as well as colocalization of E-selectin with CCL17 and ICAM-1. Coexpression of these molecules on blood vessels in noninflamed skin provides the basis for a model of cutaneous immunosurveillance system active in the absence of pathologic inflammation.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.172.3.1575</identifier><identifier>PMID: 14734737</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>CCL17 protein ; Cell Movement - immunology ; Chemokine CCL17 ; Chemokines, CC - biosynthesis ; Chemokines, CC - metabolism ; Chemokines, CC - physiology ; Confocal multicolor immunofluorescence imaging ; E-Selectin - biosynthesis ; E-Selectin - metabolism ; E-Selectin - physiology ; Endothelium, Vascular - immunology ; Endothelium, Vascular - metabolism ; Humans ; Immunohistochemistry ; Immunologic Memory ; intercellular adhesion molecule 1 ; Intercellular Adhesion Molecule-1 - biosynthesis ; Intercellular Adhesion Molecule-1 - metabolism ; Intercellular Adhesion Molecule-1 - physiology ; LFA-1 antigen ; Lymphocyte Activation - immunology ; Microcirculation - immunology ; Microcirculation - metabolism ; Microscopy, Fluorescence ; Models, Immunological ; Monitoring, Immunologic ; Platelet Endothelial Cell Adhesion Molecule-1 - metabolism ; Skin - blood supply ; Skin - immunology ; Skin - metabolism ; T-Lymphocyte Subsets - immunology ; T-Lymphocyte Subsets - metabolism ; Thymus Gland - cytology ; Thymus Gland - immunology ; Thymus Gland - metabolism</subject><ispartof>The Journal of immunology (1950), 2004-02, Vol.172 (3), p.1575-1581</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-b6634dd4bb45dd444b78f8b7870a22e7ed4fd3239586b2887610a7eea23fb4b43</citedby><cites>FETCH-LOGICAL-c475t-b6634dd4bb45dd444b78f8b7870a22e7ed4fd3239586b2887610a7eea23fb4b43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14734737$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chong, Benjamin F</creatorcontrib><creatorcontrib>Murphy, Jo-Ellen</creatorcontrib><creatorcontrib>Kupper, Thomas S</creatorcontrib><creatorcontrib>Fuhlbrigge, Robert C</creatorcontrib><title>E-Selectin, Thymus- and Activation-Regulated Chemokine/CCL17, and Intercellular Adhesion Molecule-1 Are Constitutively Coexpressed in Dermal Microvessels: A Foundation for a Cutaneous Immunosurveillance System</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>The success of the cutaneous immune system reflects its ability to rapidly and efficiently recruit leukocytes to areas of trauma and infection. Skin-homing memory T cells expressing cutaneous lymphocyte-associated Ag tether on the walls of postcapillary venules in inflamed skin via interaction with endothelial E-selectin and roll in response to the shear stress imparted by flowing blood. Rolling cells sample the vascular surface for chemoattractant compounds (e.g., thymus- and activation-regulated chemokine/CCL17 interacting with CCR4 on the leukocyte surface) and, if successfully stimulated, progress to firm arrest and transmigration mediated by LFA-1 and vascular ICAM-1. Although it is established that this sequence of events draws T cells into inflamed skin, the mechanisms directing trafficking of T cells to noninflamed skin are less well characterized. We hypothesized that basal expression and colocalization of E-selectin, chemokine (e.g., CCL17), and ICAM-1 in dermal vessels could serve to recruit T cells to noninflamed human skin. Immunohistochemical staining for E-selectin and CD31 demonstrated E-selectin expression in a restricted subset of dermal vessels in noninflamed human skin from three different sites. Confocal multicolor immunofluorescence imaging revealed a nonuniform distribution of E-selectin in dermal vessels as well as colocalization of E-selectin with CCL17 and ICAM-1. Coexpression of these molecules on blood vessels in noninflamed skin provides the basis for a model of cutaneous immunosurveillance system active in the absence of pathologic inflammation.</description><subject>CCL17 protein</subject><subject>Cell Movement - immunology</subject><subject>Chemokine CCL17</subject><subject>Chemokines, CC - biosynthesis</subject><subject>Chemokines, CC - metabolism</subject><subject>Chemokines, CC - physiology</subject><subject>Confocal multicolor immunofluorescence imaging</subject><subject>E-Selectin - biosynthesis</subject><subject>E-Selectin - metabolism</subject><subject>E-Selectin - physiology</subject><subject>Endothelium, Vascular - immunology</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Immunologic Memory</subject><subject>intercellular adhesion molecule 1</subject><subject>Intercellular Adhesion Molecule-1 - biosynthesis</subject><subject>Intercellular Adhesion Molecule-1 - metabolism</subject><subject>Intercellular Adhesion Molecule-1 - physiology</subject><subject>LFA-1 antigen</subject><subject>Lymphocyte Activation - immunology</subject><subject>Microcirculation - immunology</subject><subject>Microcirculation - metabolism</subject><subject>Microscopy, Fluorescence</subject><subject>Models, Immunological</subject><subject>Monitoring, Immunologic</subject><subject>Platelet Endothelial Cell Adhesion Molecule-1 - metabolism</subject><subject>Skin - blood supply</subject><subject>Skin - immunology</subject><subject>Skin - metabolism</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocyte Subsets - metabolism</subject><subject>Thymus Gland - cytology</subject><subject>Thymus Gland - immunology</subject><subject>Thymus Gland - metabolism</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkd1u1DAQhSMEokvhCZCQr-Cm2fovcZa7KLSw0lZItFxbTjJpXBxna8e77GP2jer9QXCHZHnk0TdH43OS5D3Bc4754vJBD0Owo5kTQedsTjKRvUhmJMtwmuc4f5nMMKY0JSIXZ8kb7x8wxjmm_HVyRrhg8YhZ8nSV3oKBZtL2At31uyH4FCnbojK2NmrSo01_wH0waoIWVT0M4y9t4bKqVkRcHMilncA1YEyEHCrbHnycQjdjlA0GUoJKB6garZ_0FKIqmF18wu-1A--jqrboC7hBGXSjGzdu9l3jP6MSXY_BtoclUDc6pFAVJmVhDB4tD5_3wW1AG6NsA-h25ycY3iavOmU8vDvV8-Tn9dVd9S1dff-6rMpV2nCRTWmd54y3La9rnsXCeS2KroiXwIpSENDyrmWULbIir2lRiJxgJQAUZV3Na87Ok49H3bUbHwP4SQ7a7204LigLTEieMfJfkCwooxkuIsiOYDTBewedXDs9KLeTBMt95PJP5DJGLpncRx6nPpzkQz1A-3fmlHEEPh2BXt_3W-1A-ui1iTiR2-32H6lnC6-7bA</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Chong, Benjamin F</creator><creator>Murphy, Jo-Ellen</creator><creator>Kupper, Thomas S</creator><creator>Fuhlbrigge, Robert C</creator><general>Am Assoc Immnol</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>H94</scope><scope>7X8</scope></search><sort><creationdate>20040201</creationdate><title>E-Selectin, Thymus- and Activation-Regulated Chemokine/CCL17, and Intercellular Adhesion Molecule-1 Are Constitutively Coexpressed in Dermal Microvessels: A Foundation for a Cutaneous Immunosurveillance System</title><author>Chong, Benjamin F ; Murphy, Jo-Ellen ; Kupper, Thomas S ; Fuhlbrigge, Robert C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-b6634dd4bb45dd444b78f8b7870a22e7ed4fd3239586b2887610a7eea23fb4b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>CCL17 protein</topic><topic>Cell Movement - immunology</topic><topic>Chemokine CCL17</topic><topic>Chemokines, CC - biosynthesis</topic><topic>Chemokines, CC - metabolism</topic><topic>Chemokines, CC - physiology</topic><topic>Confocal multicolor immunofluorescence imaging</topic><topic>E-Selectin - biosynthesis</topic><topic>E-Selectin - metabolism</topic><topic>E-Selectin - physiology</topic><topic>Endothelium, Vascular - immunology</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunologic Memory</topic><topic>intercellular adhesion molecule 1</topic><topic>Intercellular Adhesion Molecule-1 - biosynthesis</topic><topic>Intercellular Adhesion Molecule-1 - metabolism</topic><topic>Intercellular Adhesion Molecule-1 - physiology</topic><topic>LFA-1 antigen</topic><topic>Lymphocyte Activation - immunology</topic><topic>Microcirculation - immunology</topic><topic>Microcirculation - metabolism</topic><topic>Microscopy, Fluorescence</topic><topic>Models, Immunological</topic><topic>Monitoring, Immunologic</topic><topic>Platelet Endothelial Cell Adhesion Molecule-1 - metabolism</topic><topic>Skin - blood supply</topic><topic>Skin - immunology</topic><topic>Skin - metabolism</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocyte Subsets - metabolism</topic><topic>Thymus Gland - cytology</topic><topic>Thymus Gland - immunology</topic><topic>Thymus Gland - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chong, Benjamin F</creatorcontrib><creatorcontrib>Murphy, Jo-Ellen</creatorcontrib><creatorcontrib>Kupper, Thomas S</creatorcontrib><creatorcontrib>Fuhlbrigge, Robert C</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>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chong, Benjamin F</au><au>Murphy, Jo-Ellen</au><au>Kupper, Thomas S</au><au>Fuhlbrigge, Robert C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>E-Selectin, Thymus- and Activation-Regulated Chemokine/CCL17, and Intercellular Adhesion Molecule-1 Are Constitutively Coexpressed in Dermal Microvessels: A Foundation for a Cutaneous Immunosurveillance System</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2004-02-01</date><risdate>2004</risdate><volume>172</volume><issue>3</issue><spage>1575</spage><epage>1581</epage><pages>1575-1581</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>The success of the cutaneous immune system reflects its ability to rapidly and efficiently recruit leukocytes to areas of trauma and infection. Skin-homing memory T cells expressing cutaneous lymphocyte-associated Ag tether on the walls of postcapillary venules in inflamed skin via interaction with endothelial E-selectin and roll in response to the shear stress imparted by flowing blood. Rolling cells sample the vascular surface for chemoattractant compounds (e.g., thymus- and activation-regulated chemokine/CCL17 interacting with CCR4 on the leukocyte surface) and, if successfully stimulated, progress to firm arrest and transmigration mediated by LFA-1 and vascular ICAM-1. Although it is established that this sequence of events draws T cells into inflamed skin, the mechanisms directing trafficking of T cells to noninflamed skin are less well characterized. We hypothesized that basal expression and colocalization of E-selectin, chemokine (e.g., CCL17), and ICAM-1 in dermal vessels could serve to recruit T cells to noninflamed human skin. Immunohistochemical staining for E-selectin and CD31 demonstrated E-selectin expression in a restricted subset of dermal vessels in noninflamed human skin from three different sites. Confocal multicolor immunofluorescence imaging revealed a nonuniform distribution of E-selectin in dermal vessels as well as colocalization of E-selectin with CCL17 and ICAM-1. Coexpression of these molecules on blood vessels in noninflamed skin provides the basis for a model of cutaneous immunosurveillance system active in the absence of pathologic inflammation.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>14734737</pmid><doi>10.4049/jimmunol.172.3.1575</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1767 |
ispartof | The Journal of immunology (1950), 2004-02, Vol.172 (3), p.1575-1581 |
issn | 0022-1767 1550-6606 |
language | eng |
recordid | cdi_proquest_miscellaneous_80116531 |
source | EZB Electronic Journals Library |
subjects | CCL17 protein Cell Movement - immunology Chemokine CCL17 Chemokines, CC - biosynthesis Chemokines, CC - metabolism Chemokines, CC - physiology Confocal multicolor immunofluorescence imaging E-Selectin - biosynthesis E-Selectin - metabolism E-Selectin - physiology Endothelium, Vascular - immunology Endothelium, Vascular - metabolism Humans Immunohistochemistry Immunologic Memory intercellular adhesion molecule 1 Intercellular Adhesion Molecule-1 - biosynthesis Intercellular Adhesion Molecule-1 - metabolism Intercellular Adhesion Molecule-1 - physiology LFA-1 antigen Lymphocyte Activation - immunology Microcirculation - immunology Microcirculation - metabolism Microscopy, Fluorescence Models, Immunological Monitoring, Immunologic Platelet Endothelial Cell Adhesion Molecule-1 - metabolism Skin - blood supply Skin - immunology Skin - metabolism T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism Thymus Gland - cytology Thymus Gland - immunology Thymus Gland - metabolism |
title | E-Selectin, Thymus- and Activation-Regulated Chemokine/CCL17, and Intercellular Adhesion Molecule-1 Are Constitutively Coexpressed in Dermal Microvessels: A Foundation for a Cutaneous Immunosurveillance System |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T03%3A31%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=E-Selectin,%20Thymus-%20and%20Activation-Regulated%20Chemokine/CCL17,%20and%20Intercellular%20Adhesion%20Molecule-1%20Are%20Constitutively%20Coexpressed%20in%20Dermal%20Microvessels:%20A%20Foundation%20for%20a%20Cutaneous%20Immunosurveillance%20System&rft.jtitle=The%20Journal%20of%20immunology%20(1950)&rft.au=Chong,%20Benjamin%20F&rft.date=2004-02-01&rft.volume=172&rft.issue=3&rft.spage=1575&rft.epage=1581&rft.pages=1575-1581&rft.issn=0022-1767&rft.eissn=1550-6606&rft_id=info:doi/10.4049/jimmunol.172.3.1575&rft_dat=%3Cproquest_cross%3E19232508%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c475t-b6634dd4bb45dd444b78f8b7870a22e7ed4fd3239586b2887610a7eea23fb4b43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=19232508&rft_id=info:pmid/14734737&rfr_iscdi=true |