Professional Memory CD4 + T Lymphocytes Preferentially Reside and Rest in the Bone Marrow

CD4 + T lymphocytes are key to immunological memory. Here we show that in the memory phase of specific immune responses, most of the memory CD4 + T lymphocytes had relocated into the bone marrow (BM) within 3–8 weeks after their generation—a process involving integrin α2. Antigen-specific memory CD4...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Immunity (Cambridge, Mass.) Mass.), 2009-05, Vol.30 (5), p.721-730
Hauptverfasser: Tokoyoda, Koji, Zehentmeier, Sandra, Hegazy, Ahmed N., Albrecht, Inka, Grün, Joachim R., Löhning, Max, Radbruch, Andreas
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 730
container_issue 5
container_start_page 721
container_title Immunity (Cambridge, Mass.)
container_volume 30
creator Tokoyoda, Koji
Zehentmeier, Sandra
Hegazy, Ahmed N.
Albrecht, Inka
Grün, Joachim R.
Löhning, Max
Radbruch, Andreas
description CD4 + T lymphocytes are key to immunological memory. Here we show that in the memory phase of specific immune responses, most of the memory CD4 + T lymphocytes had relocated into the bone marrow (BM) within 3–8 weeks after their generation—a process involving integrin α2. Antigen-specific memory CD4 + T lymphocytes highly expressed Ly-6C, unlike most splenic CD44 hiCD62L − CD4 + T lymphocytes. In adult mice, more than 80% of Ly-6C hiCD44 hiCD62L − memory CD4 + T lymphocytes were in the BM. In the BM, they associated to IL-7-expressing VCAM-1 + stroma cells. Gene expression and proliferation were downregulated, indicating a resting state. Upon challenge with antigen, they rapidly expressed cytokines and CD154 and efficiently induced the production of high-affinity antibodies by B lymphocytes. Thus, in the memory phase of immunity, memory helper T cells are maintained in BM as resting but highly reactive cells in survival niches defined by IL-7-expressing stroma cells.
doi_str_mv 10.1016/j.immuni.2009.03.015
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67286570</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1074761309001873</els_id><sourcerecordid>3236862951</sourcerecordid><originalsourceid>FETCH-LOGICAL-c434t-6a09ab26a2b706a418a74cbe3496dcda8f861fbba130ee6822909900ef990a93</originalsourceid><addsrcrecordid>eNp9kEtr3DAQgEVoSdKk_yAEQaGXYmcky7J1KbTbV2BDQthLT0KWx0SLbW0lO8X_Plp2odBDLjNz-Ob1EXLFIGfA5M02d8Mwjy7nACqHIgdWnpBzBqrKBKvhzb6uRFZJVpyRdzFuAZgoFZySM6YEr7jg5-T3Q_Adxuj8aHp6h4MPC119E_QT3dD1MuyevF0mjPQhYIcBx8mZvl_oI0bXIjVjuy8n6kY6PSH96kekdyYE__eSvO1MH_H9MV-QzY_vm9WvbH3_83b1ZZ1ZUYgpkwaUabg0vKlAmnS5qYRtsBBKtrY1dVdL1jWNYQUgyppzBUoBYJeiUcUF-XgYuwv-z5xO0YOLFvvejOjnqGXFa1lWkMAP_4FbP4f0ddSsBMFlmVYmShwoG3yM6We9C24wYdEM9N673uqDd733rqHQyXtquz4On5sB239NR9EJ-HwAMKl4dhh0tA5Hi60LaCfdevf6hhfAPpRq</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1504265349</pqid></control><display><type>article</type><title>Professional Memory CD4 + T Lymphocytes Preferentially Reside and Rest in the Bone Marrow</title><source>MEDLINE</source><source>Cell Press Free Archives</source><source>Elsevier ScienceDirect Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Tokoyoda, Koji ; Zehentmeier, Sandra ; Hegazy, Ahmed N. ; Albrecht, Inka ; Grün, Joachim R. ; Löhning, Max ; Radbruch, Andreas</creator><creatorcontrib>Tokoyoda, Koji ; Zehentmeier, Sandra ; Hegazy, Ahmed N. ; Albrecht, Inka ; Grün, Joachim R. ; Löhning, Max ; Radbruch, Andreas</creatorcontrib><description>CD4 + T lymphocytes are key to immunological memory. Here we show that in the memory phase of specific immune responses, most of the memory CD4 + T lymphocytes had relocated into the bone marrow (BM) within 3–8 weeks after their generation—a process involving integrin α2. Antigen-specific memory CD4 + T lymphocytes highly expressed Ly-6C, unlike most splenic CD44 hiCD62L − CD4 + T lymphocytes. In adult mice, more than 80% of Ly-6C hiCD44 hiCD62L − memory CD4 + T lymphocytes were in the BM. In the BM, they associated to IL-7-expressing VCAM-1 + stroma cells. Gene expression and proliferation were downregulated, indicating a resting state. Upon challenge with antigen, they rapidly expressed cytokines and CD154 and efficiently induced the production of high-affinity antibodies by B lymphocytes. Thus, in the memory phase of immunity, memory helper T cells are maintained in BM as resting but highly reactive cells in survival niches defined by IL-7-expressing stroma cells.</description><identifier>ISSN: 1074-7613</identifier><identifier>EISSN: 1097-4180</identifier><identifier>DOI: 10.1016/j.immuni.2009.03.015</identifier><identifier>PMID: 19427242</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antigens ; Antigens, Ly - immunology ; B-Lymphocytes - immunology ; Bone Marrow - immunology ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - metabolism ; CELLIMMUNO ; Competition ; Down-Regulation - immunology ; Gene Expression ; Homeostasis ; Immune system ; Immunologic Memory ; Integrin alpha2 - immunology ; Interleukin-7 - immunology ; Interleukin-7 - metabolism ; Lymphocytes ; Mice ; Microscopy ; Oligonucleotide Array Sequence Analysis ; Plasma ; Spleen ; Stromal Cells - immunology ; Stromal Cells - metabolism ; T cell receptors</subject><ispartof>Immunity (Cambridge, Mass.), 2009-05, Vol.30 (5), p.721-730</ispartof><rights>2009 Elsevier Inc.</rights><rights>Copyright Elsevier Limited May 22, 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-6a09ab26a2b706a418a74cbe3496dcda8f861fbba130ee6822909900ef990a93</citedby><cites>FETCH-LOGICAL-c434t-6a09ab26a2b706a418a74cbe3496dcda8f861fbba130ee6822909900ef990a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1074761309001873$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19427242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tokoyoda, Koji</creatorcontrib><creatorcontrib>Zehentmeier, Sandra</creatorcontrib><creatorcontrib>Hegazy, Ahmed N.</creatorcontrib><creatorcontrib>Albrecht, Inka</creatorcontrib><creatorcontrib>Grün, Joachim R.</creatorcontrib><creatorcontrib>Löhning, Max</creatorcontrib><creatorcontrib>Radbruch, Andreas</creatorcontrib><title>Professional Memory CD4 + T Lymphocytes Preferentially Reside and Rest in the Bone Marrow</title><title>Immunity (Cambridge, Mass.)</title><addtitle>Immunity</addtitle><description>CD4 + T lymphocytes are key to immunological memory. Here we show that in the memory phase of specific immune responses, most of the memory CD4 + T lymphocytes had relocated into the bone marrow (BM) within 3–8 weeks after their generation—a process involving integrin α2. Antigen-specific memory CD4 + T lymphocytes highly expressed Ly-6C, unlike most splenic CD44 hiCD62L − CD4 + T lymphocytes. In adult mice, more than 80% of Ly-6C hiCD44 hiCD62L − memory CD4 + T lymphocytes were in the BM. In the BM, they associated to IL-7-expressing VCAM-1 + stroma cells. Gene expression and proliferation were downregulated, indicating a resting state. Upon challenge with antigen, they rapidly expressed cytokines and CD154 and efficiently induced the production of high-affinity antibodies by B lymphocytes. Thus, in the memory phase of immunity, memory helper T cells are maintained in BM as resting but highly reactive cells in survival niches defined by IL-7-expressing stroma cells.</description><subject>Animals</subject><subject>Antigens</subject><subject>Antigens, Ly - immunology</subject><subject>B-Lymphocytes - immunology</subject><subject>Bone Marrow - immunology</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>CELLIMMUNO</subject><subject>Competition</subject><subject>Down-Regulation - immunology</subject><subject>Gene Expression</subject><subject>Homeostasis</subject><subject>Immune system</subject><subject>Immunologic Memory</subject><subject>Integrin alpha2 - immunology</subject><subject>Interleukin-7 - immunology</subject><subject>Interleukin-7 - metabolism</subject><subject>Lymphocytes</subject><subject>Mice</subject><subject>Microscopy</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Plasma</subject><subject>Spleen</subject><subject>Stromal Cells - immunology</subject><subject>Stromal Cells - metabolism</subject><subject>T cell receptors</subject><issn>1074-7613</issn><issn>1097-4180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtr3DAQgEVoSdKk_yAEQaGXYmcky7J1KbTbV2BDQthLT0KWx0SLbW0lO8X_Plp2odBDLjNz-Ob1EXLFIGfA5M02d8Mwjy7nACqHIgdWnpBzBqrKBKvhzb6uRFZJVpyRdzFuAZgoFZySM6YEr7jg5-T3Q_Adxuj8aHp6h4MPC119E_QT3dD1MuyevF0mjPQhYIcBx8mZvl_oI0bXIjVjuy8n6kY6PSH96kekdyYE__eSvO1MH_H9MV-QzY_vm9WvbH3_83b1ZZ1ZUYgpkwaUabg0vKlAmnS5qYRtsBBKtrY1dVdL1jWNYQUgyppzBUoBYJeiUcUF-XgYuwv-z5xO0YOLFvvejOjnqGXFa1lWkMAP_4FbP4f0ddSsBMFlmVYmShwoG3yM6We9C24wYdEM9N673uqDd733rqHQyXtquz4On5sB239NR9EJ-HwAMKl4dhh0tA5Hi60LaCfdevf6hhfAPpRq</recordid><startdate>20090522</startdate><enddate>20090522</enddate><creator>Tokoyoda, Koji</creator><creator>Zehentmeier, Sandra</creator><creator>Hegazy, Ahmed N.</creator><creator>Albrecht, Inka</creator><creator>Grün, Joachim R.</creator><creator>Löhning, Max</creator><creator>Radbruch, Andreas</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20090522</creationdate><title>Professional Memory CD4 + T Lymphocytes Preferentially Reside and Rest in the Bone Marrow</title><author>Tokoyoda, Koji ; Zehentmeier, Sandra ; Hegazy, Ahmed N. ; Albrecht, Inka ; Grün, Joachim R. ; Löhning, Max ; Radbruch, Andreas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-6a09ab26a2b706a418a74cbe3496dcda8f861fbba130ee6822909900ef990a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Antigens</topic><topic>Antigens, Ly - immunology</topic><topic>B-Lymphocytes - immunology</topic><topic>Bone Marrow - immunology</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - metabolism</topic><topic>CELLIMMUNO</topic><topic>Competition</topic><topic>Down-Regulation - immunology</topic><topic>Gene Expression</topic><topic>Homeostasis</topic><topic>Immune system</topic><topic>Immunologic Memory</topic><topic>Integrin alpha2 - immunology</topic><topic>Interleukin-7 - immunology</topic><topic>Interleukin-7 - metabolism</topic><topic>Lymphocytes</topic><topic>Mice</topic><topic>Microscopy</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Plasma</topic><topic>Spleen</topic><topic>Stromal Cells - immunology</topic><topic>Stromal Cells - metabolism</topic><topic>T cell receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tokoyoda, Koji</creatorcontrib><creatorcontrib>Zehentmeier, Sandra</creatorcontrib><creatorcontrib>Hegazy, Ahmed N.</creatorcontrib><creatorcontrib>Albrecht, Inka</creatorcontrib><creatorcontrib>Grün, Joachim R.</creatorcontrib><creatorcontrib>Löhning, Max</creatorcontrib><creatorcontrib>Radbruch, Andreas</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Immunity (Cambridge, Mass.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tokoyoda, Koji</au><au>Zehentmeier, Sandra</au><au>Hegazy, Ahmed N.</au><au>Albrecht, Inka</au><au>Grün, Joachim R.</au><au>Löhning, Max</au><au>Radbruch, Andreas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Professional Memory CD4 + T Lymphocytes Preferentially Reside and Rest in the Bone Marrow</atitle><jtitle>Immunity (Cambridge, Mass.)</jtitle><addtitle>Immunity</addtitle><date>2009-05-22</date><risdate>2009</risdate><volume>30</volume><issue>5</issue><spage>721</spage><epage>730</epage><pages>721-730</pages><issn>1074-7613</issn><eissn>1097-4180</eissn><abstract>CD4 + T lymphocytes are key to immunological memory. Here we show that in the memory phase of specific immune responses, most of the memory CD4 + T lymphocytes had relocated into the bone marrow (BM) within 3–8 weeks after their generation—a process involving integrin α2. Antigen-specific memory CD4 + T lymphocytes highly expressed Ly-6C, unlike most splenic CD44 hiCD62L − CD4 + T lymphocytes. In adult mice, more than 80% of Ly-6C hiCD44 hiCD62L − memory CD4 + T lymphocytes were in the BM. In the BM, they associated to IL-7-expressing VCAM-1 + stroma cells. Gene expression and proliferation were downregulated, indicating a resting state. Upon challenge with antigen, they rapidly expressed cytokines and CD154 and efficiently induced the production of high-affinity antibodies by B lymphocytes. Thus, in the memory phase of immunity, memory helper T cells are maintained in BM as resting but highly reactive cells in survival niches defined by IL-7-expressing stroma cells.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19427242</pmid><doi>10.1016/j.immuni.2009.03.015</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1074-7613
ispartof Immunity (Cambridge, Mass.), 2009-05, Vol.30 (5), p.721-730
issn 1074-7613
1097-4180
language eng
recordid cdi_proquest_miscellaneous_67286570
source MEDLINE; Cell Press Free Archives; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Animals
Antigens
Antigens, Ly - immunology
B-Lymphocytes - immunology
Bone Marrow - immunology
CD4-Positive T-Lymphocytes - immunology
CD4-Positive T-Lymphocytes - metabolism
CELLIMMUNO
Competition
Down-Regulation - immunology
Gene Expression
Homeostasis
Immune system
Immunologic Memory
Integrin alpha2 - immunology
Interleukin-7 - immunology
Interleukin-7 - metabolism
Lymphocytes
Mice
Microscopy
Oligonucleotide Array Sequence Analysis
Plasma
Spleen
Stromal Cells - immunology
Stromal Cells - metabolism
T cell receptors
title Professional Memory CD4 + T Lymphocytes Preferentially Reside and Rest in the Bone Marrow
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T02%3A16%3A37IST&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=Professional%20Memory%20CD4%20+%20T%20Lymphocytes%20Preferentially%20Reside%20and%20Rest%20in%20the%20Bone%20Marrow&rft.jtitle=Immunity%20(Cambridge,%20Mass.)&rft.au=Tokoyoda,%20Koji&rft.date=2009-05-22&rft.volume=30&rft.issue=5&rft.spage=721&rft.epage=730&rft.pages=721-730&rft.issn=1074-7613&rft.eissn=1097-4180&rft_id=info:doi/10.1016/j.immuni.2009.03.015&rft_dat=%3Cproquest_cross%3E3236862951%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1504265349&rft_id=info:pmid/19427242&rft_els_id=S1074761309001873&rfr_iscdi=true