Selective Thymus Settling Regulated by Cytokine and Chemokine Receptors
To generate T cells throughout adult life, the thymus must import hemopoietic progenitors from the bone marrow via the blood. In this study, we establish that thymus settling is selective. Using nonirradiated recipient mice, we found that hemopoietic stem cells were excluded from the thymus, whereas...
Gespeichert in:
Veröffentlicht in: | Journal of Immunology 2007-02, Vol.178 (4), p.2008-2017 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2017 |
---|---|
container_issue | 4 |
container_start_page | 2008 |
container_title | Journal of Immunology |
container_volume | 178 |
creator | Schwarz, Benjamin A Sambandam, Arivazhagan Maillard, Ivan Harman, Benjamin C Love, Paul E Bhandoola, Avinash |
description | To generate T cells throughout adult life, the thymus must import hemopoietic progenitors from the bone marrow via the blood. In this study, we establish that thymus settling is selective. Using nonirradiated recipient mice, we found that hemopoietic stem cells were excluded from the thymus, whereas downstream multipotent progenitors (MPP) and common lymphoid progenitors rapidly generated T cells following i.v. transfer. This cellular specificity correlated with the expression of the chemokine receptor CCR9 by a subset of MPP and common lymphoid progenitors but not hemopoietic stem cells. Furthermore, CCR9 expression was required for efficient thymus settling. Finally, we demonstrate that a prethymic signal through the cytokine receptor fms-like tyrosine kinase receptor-3 was required for the generation of CCR9-expressing early lymphoid progenitors, which were the most efficient progenitors of T cells within the MPP population. We conclude that fms-like tyrosine kinase receptor-3 signaling is required for the generation of T lineage-competent progenitors, which selectively express molecules, including CCR9, that allow them to settle within the thymus. |
doi_str_mv | 10.4049/jimmunol.178.4.2008 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68975799</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19586592</sourcerecordid><originalsourceid>FETCH-LOGICAL-c477t-76c7c99921692df0b7326e44fe58bef733372380c46237e331330e6e10c1cbc03</originalsourceid><addsrcrecordid>eNqFkEtLw0AURgdRbH38AkGy0lXqnUdmMkspWoWC0Nb1kExv2tRJUjOJof_elFZ05-py4XxncQi5oTASIPTDJi-KtqzciKp4JEYMID4hQxpFEEoJ8pQMARgLqZJqQC683wCABCbOyYAqphQFMSSTOTq0Tf6FwWK9K1ofzLFpXF6ughmuWpc0uAzSXTDeNdVHXmKQlMtgvMbi8M3Q4rapan9FzrLEebw-3kvy_vy0GL-E07fJ6_hxGlqhVBMqaZXVWjMqNVtmkCrOJAqRYRSnmCnOuWI8Bisk4wo5p5wDSqRgqU0t8Etyd_Bu6-qzRd-YIvcWnUtKrFpvZKxVpLT-F6Q6imWkWQ_yA2jryvsaM7Ot8yKpd4aC2Yc2P6FNH9oIsw_dr26P-jYtcPm7OZbtgfsDsM5X6y6v0fgica7Hqem67o_qG3_biFs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19586592</pqid></control><display><type>article</type><title>Selective Thymus Settling Regulated by Cytokine and Chemokine Receptors</title><source>Wiley Free Content</source><source>MEDLINE</source><source>IngentaConnect Free/Open Access Journals</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Schwarz, Benjamin A ; Sambandam, Arivazhagan ; Maillard, Ivan ; Harman, Benjamin C ; Love, Paul E ; Bhandoola, Avinash</creator><creatorcontrib>Schwarz, Benjamin A ; Sambandam, Arivazhagan ; Maillard, Ivan ; Harman, Benjamin C ; Love, Paul E ; Bhandoola, Avinash</creatorcontrib><description>To generate T cells throughout adult life, the thymus must import hemopoietic progenitors from the bone marrow via the blood. In this study, we establish that thymus settling is selective. Using nonirradiated recipient mice, we found that hemopoietic stem cells were excluded from the thymus, whereas downstream multipotent progenitors (MPP) and common lymphoid progenitors rapidly generated T cells following i.v. transfer. This cellular specificity correlated with the expression of the chemokine receptor CCR9 by a subset of MPP and common lymphoid progenitors but not hemopoietic stem cells. Furthermore, CCR9 expression was required for efficient thymus settling. Finally, we demonstrate that a prethymic signal through the cytokine receptor fms-like tyrosine kinase receptor-3 was required for the generation of CCR9-expressing early lymphoid progenitors, which were the most efficient progenitors of T cells within the MPP population. We conclude that fms-like tyrosine kinase receptor-3 signaling is required for the generation of T lineage-competent progenitors, which selectively express molecules, including CCR9, that allow them to settle within the thymus.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>EISSN: 1365-2567</identifier><identifier>DOI: 10.4049/jimmunol.178.4.2008</identifier><identifier>PMID: 17277104</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Animals ; Bone Marrow Transplantation ; Cell Differentiation - immunology ; Cell Movement - immunology ; Cytokines - immunology ; Hematopoietic Stem Cells - cytology ; Hematopoietic Stem Cells - immunology ; Mice ; Multipotent Stem Cells - cytology ; Multipotent Stem Cells - immunology ; Receptors, CCR ; Receptors, Chemokine - immunology ; Signal Transduction - immunology ; T-Lymphocytes - cytology ; T-Lymphocytes - immunology ; Thymus Gland - cytology ; Thymus Gland - immunology ; Vascular Endothelial Growth Factor Receptor-1 - immunology ; Whole-Body Irradiation</subject><ispartof>Journal of Immunology, 2007-02, Vol.178 (4), p.2008-2017</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c477t-76c7c99921692df0b7326e44fe58bef733372380c46237e331330e6e10c1cbc03</citedby><cites>FETCH-LOGICAL-c477t-76c7c99921692df0b7326e44fe58bef733372380c46237e331330e6e10c1cbc03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17277104$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schwarz, Benjamin A</creatorcontrib><creatorcontrib>Sambandam, Arivazhagan</creatorcontrib><creatorcontrib>Maillard, Ivan</creatorcontrib><creatorcontrib>Harman, Benjamin C</creatorcontrib><creatorcontrib>Love, Paul E</creatorcontrib><creatorcontrib>Bhandoola, Avinash</creatorcontrib><title>Selective Thymus Settling Regulated by Cytokine and Chemokine Receptors</title><title>Journal of Immunology</title><addtitle>J Immunol</addtitle><description>To generate T cells throughout adult life, the thymus must import hemopoietic progenitors from the bone marrow via the blood. In this study, we establish that thymus settling is selective. Using nonirradiated recipient mice, we found that hemopoietic stem cells were excluded from the thymus, whereas downstream multipotent progenitors (MPP) and common lymphoid progenitors rapidly generated T cells following i.v. transfer. This cellular specificity correlated with the expression of the chemokine receptor CCR9 by a subset of MPP and common lymphoid progenitors but not hemopoietic stem cells. Furthermore, CCR9 expression was required for efficient thymus settling. Finally, we demonstrate that a prethymic signal through the cytokine receptor fms-like tyrosine kinase receptor-3 was required for the generation of CCR9-expressing early lymphoid progenitors, which were the most efficient progenitors of T cells within the MPP population. We conclude that fms-like tyrosine kinase receptor-3 signaling is required for the generation of T lineage-competent progenitors, which selectively express molecules, including CCR9, that allow them to settle within the thymus.</description><subject>Animals</subject><subject>Bone Marrow Transplantation</subject><subject>Cell Differentiation - immunology</subject><subject>Cell Movement - immunology</subject><subject>Cytokines - immunology</subject><subject>Hematopoietic Stem Cells - cytology</subject><subject>Hematopoietic Stem Cells - immunology</subject><subject>Mice</subject><subject>Multipotent Stem Cells - cytology</subject><subject>Multipotent Stem Cells - immunology</subject><subject>Receptors, CCR</subject><subject>Receptors, Chemokine - immunology</subject><subject>Signal Transduction - immunology</subject><subject>T-Lymphocytes - cytology</subject><subject>T-Lymphocytes - immunology</subject><subject>Thymus Gland - cytology</subject><subject>Thymus Gland - immunology</subject><subject>Vascular Endothelial Growth Factor Receptor-1 - immunology</subject><subject>Whole-Body Irradiation</subject><issn>0022-1767</issn><issn>1550-6606</issn><issn>1365-2567</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLw0AURgdRbH38AkGy0lXqnUdmMkspWoWC0Nb1kExv2tRJUjOJof_elFZ05-py4XxncQi5oTASIPTDJi-KtqzciKp4JEYMID4hQxpFEEoJ8pQMARgLqZJqQC683wCABCbOyYAqphQFMSSTOTq0Tf6FwWK9K1ofzLFpXF6ughmuWpc0uAzSXTDeNdVHXmKQlMtgvMbi8M3Q4rapan9FzrLEebw-3kvy_vy0GL-E07fJ6_hxGlqhVBMqaZXVWjMqNVtmkCrOJAqRYRSnmCnOuWI8Bisk4wo5p5wDSqRgqU0t8Etyd_Bu6-qzRd-YIvcWnUtKrFpvZKxVpLT-F6Q6imWkWQ_yA2jryvsaM7Ot8yKpd4aC2Yc2P6FNH9oIsw_dr26P-jYtcPm7OZbtgfsDsM5X6y6v0fgica7Hqem67o_qG3_biFs</recordid><startdate>20070215</startdate><enddate>20070215</enddate><creator>Schwarz, Benjamin A</creator><creator>Sambandam, Arivazhagan</creator><creator>Maillard, Ivan</creator><creator>Harman, Benjamin C</creator><creator>Love, Paul E</creator><creator>Bhandoola, Avinash</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>20070215</creationdate><title>Selective Thymus Settling Regulated by Cytokine and Chemokine Receptors</title><author>Schwarz, Benjamin A ; Sambandam, Arivazhagan ; Maillard, Ivan ; Harman, Benjamin C ; Love, Paul E ; Bhandoola, Avinash</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c477t-76c7c99921692df0b7326e44fe58bef733372380c46237e331330e6e10c1cbc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Bone Marrow Transplantation</topic><topic>Cell Differentiation - immunology</topic><topic>Cell Movement - immunology</topic><topic>Cytokines - immunology</topic><topic>Hematopoietic Stem Cells - cytology</topic><topic>Hematopoietic Stem Cells - immunology</topic><topic>Mice</topic><topic>Multipotent Stem Cells - cytology</topic><topic>Multipotent Stem Cells - immunology</topic><topic>Receptors, CCR</topic><topic>Receptors, Chemokine - immunology</topic><topic>Signal Transduction - immunology</topic><topic>T-Lymphocytes - cytology</topic><topic>T-Lymphocytes - immunology</topic><topic>Thymus Gland - cytology</topic><topic>Thymus Gland - immunology</topic><topic>Vascular Endothelial Growth Factor Receptor-1 - immunology</topic><topic>Whole-Body Irradiation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwarz, Benjamin A</creatorcontrib><creatorcontrib>Sambandam, Arivazhagan</creatorcontrib><creatorcontrib>Maillard, Ivan</creatorcontrib><creatorcontrib>Harman, Benjamin C</creatorcontrib><creatorcontrib>Love, Paul E</creatorcontrib><creatorcontrib>Bhandoola, Avinash</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>Journal of Immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwarz, Benjamin A</au><au>Sambandam, Arivazhagan</au><au>Maillard, Ivan</au><au>Harman, Benjamin C</au><au>Love, Paul E</au><au>Bhandoola, Avinash</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective Thymus Settling Regulated by Cytokine and Chemokine Receptors</atitle><jtitle>Journal of Immunology</jtitle><addtitle>J Immunol</addtitle><date>2007-02-15</date><risdate>2007</risdate><volume>178</volume><issue>4</issue><spage>2008</spage><epage>2017</epage><pages>2008-2017</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><eissn>1365-2567</eissn><abstract>To generate T cells throughout adult life, the thymus must import hemopoietic progenitors from the bone marrow via the blood. In this study, we establish that thymus settling is selective. Using nonirradiated recipient mice, we found that hemopoietic stem cells were excluded from the thymus, whereas downstream multipotent progenitors (MPP) and common lymphoid progenitors rapidly generated T cells following i.v. transfer. This cellular specificity correlated with the expression of the chemokine receptor CCR9 by a subset of MPP and common lymphoid progenitors but not hemopoietic stem cells. Furthermore, CCR9 expression was required for efficient thymus settling. Finally, we demonstrate that a prethymic signal through the cytokine receptor fms-like tyrosine kinase receptor-3 was required for the generation of CCR9-expressing early lymphoid progenitors, which were the most efficient progenitors of T cells within the MPP population. We conclude that fms-like tyrosine kinase receptor-3 signaling is required for the generation of T lineage-competent progenitors, which selectively express molecules, including CCR9, that allow them to settle within the thymus.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>17277104</pmid><doi>10.4049/jimmunol.178.4.2008</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1767 |
ispartof | Journal of Immunology, 2007-02, Vol.178 (4), p.2008-2017 |
issn | 0022-1767 1550-6606 1365-2567 |
language | eng |
recordid | cdi_proquest_miscellaneous_68975799 |
source | Wiley Free Content; MEDLINE; IngentaConnect Free/Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
subjects | Animals Bone Marrow Transplantation Cell Differentiation - immunology Cell Movement - immunology Cytokines - immunology Hematopoietic Stem Cells - cytology Hematopoietic Stem Cells - immunology Mice Multipotent Stem Cells - cytology Multipotent Stem Cells - immunology Receptors, CCR Receptors, Chemokine - immunology Signal Transduction - immunology T-Lymphocytes - cytology T-Lymphocytes - immunology Thymus Gland - cytology Thymus Gland - immunology Vascular Endothelial Growth Factor Receptor-1 - immunology Whole-Body Irradiation |
title | Selective Thymus Settling Regulated by Cytokine and Chemokine Receptors |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T23%3A26%3A50IST&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=Selective%20Thymus%20Settling%20Regulated%20by%20Cytokine%20and%20Chemokine%20Receptors&rft.jtitle=Journal%20of%20Immunology&rft.au=Schwarz,%20Benjamin%20A&rft.date=2007-02-15&rft.volume=178&rft.issue=4&rft.spage=2008&rft.epage=2017&rft.pages=2008-2017&rft.issn=0022-1767&rft.eissn=1550-6606&rft_id=info:doi/10.4049/jimmunol.178.4.2008&rft_dat=%3Cproquest_cross%3E19586592%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=19586592&rft_id=info:pmid/17277104&rfr_iscdi=true |