Loading…
NK T Cell Precursors Exhibit Differential Cytokine Regulation and Require Itk for Efficient Maturation
NK T cells are a lymphocyte lineage that is selected by CD1d and is characterized by the ability to rapidly secrete large amounts of both IFN-gamma and IL-4 after TCR stimulation. Using reactivity to CD1d tetramers to define presumptive NK T cells, several NK T cell progenitor populations were chara...
Saved in:
Published in: | The Journal of immunology (1950) 2002-09, Vol.169 (5), p.2397-2406 |
---|---|
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-c409t-ab05c0602a5968721213666ba8cab141af4cb60b6054c05ce4530d8cf028916e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c409t-ab05c0602a5968721213666ba8cab141af4cb60b6054c05ce4530d8cf028916e3 |
container_end_page | 2406 |
container_issue | 5 |
container_start_page | 2397 |
container_title | The Journal of immunology (1950) |
container_volume | 169 |
creator | Gadue, Paul Stein, Paul L |
description | NK T cells are a lymphocyte lineage that is selected by CD1d and is characterized by the ability to rapidly secrete large amounts of both IFN-gamma and IL-4 after TCR stimulation. Using reactivity to CD1d tetramers to define presumptive NK T cells, several NK T cell progenitor populations were characterized based upon NK marker expression and CD4 vs CD8 expression. The earliest populations were found to be negative for NK markers and could proliferate to IL-7, while mature NK T cells did not. The NK1.1(-) NK T cell progenitors were capable of up-regulating NK1.1 when transferred in vivo. Upon stimulation, the NK1.1(-) populations secrete IL-4, but little IFN-gamma. As the cells mature and up-regulate NK1.1, they acquire the ability to secrete IFN-gamma. Finally, the Tec family tyrosine kinase Itk is necessary for optimal NK1.1 up-regulation and hence final maturation of NK T cells. The itk(-/-) mice also display a progressive decrease in NK T cells in older animals, suggesting a further role in peripheral maintenance. |
doi_str_mv | 10.4049/jimmunol.169.5.2397 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72027944</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18470121</sourcerecordid><originalsourceid>FETCH-LOGICAL-c409t-ab05c0602a5968721213666ba8cab141af4cb60b6054c05ce4530d8cf028916e3</originalsourceid><addsrcrecordid>eNqFkUtLAzEUhYMoWqu_QJCsdDX1JpNJZpZS6wOfiK5DJk1sdB42maH6701tRXdC4BL4zrmPg9ABgREDVpy8urrum7YaEV6MshFNC7GBBiTLIOEc-CYaAFCaEMHFDtoN4RUAOFC2jXYIJUUqQAyQvbvGT3hsqgo_eKN7H1of8ORj5krX4TNnrfGm6Zyq8Piza99cY_Cjeekr1bm2waqZxu-8d97gq-4N29bjibVOuyjCt6rr_Te4h7asqoLZX9chej6fPI0vk5v7i6vx6U2iGRRdokrI9HJIlRU8FzTOmXLOS5VrVRJGlGW65BBfxnREDctSmObaAs0Lwk06REcr33ffznsTOlm7oON2qjFtH6SgQEXB2L8gyZmAZfshSleg9m0I3lj57l2t_KckIJc5yJ8cZMxBZnKZQ1Qdru37sjbTX8368BE4XgEz9zJbxPPJUKuqijiRi8Xij9UXnwaTZA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18470121</pqid></control><display><type>article</type><title>NK T Cell Precursors Exhibit Differential Cytokine Regulation and Require Itk for Efficient Maturation</title><source>Free E-Journal (出版社公開部分のみ)</source><creator>Gadue, Paul ; Stein, Paul L</creator><creatorcontrib>Gadue, Paul ; Stein, Paul L</creatorcontrib><description>NK T cells are a lymphocyte lineage that is selected by CD1d and is characterized by the ability to rapidly secrete large amounts of both IFN-gamma and IL-4 after TCR stimulation. Using reactivity to CD1d tetramers to define presumptive NK T cells, several NK T cell progenitor populations were characterized based upon NK marker expression and CD4 vs CD8 expression. The earliest populations were found to be negative for NK markers and could proliferate to IL-7, while mature NK T cells did not. The NK1.1(-) NK T cell progenitors were capable of up-regulating NK1.1 when transferred in vivo. Upon stimulation, the NK1.1(-) populations secrete IL-4, but little IFN-gamma. As the cells mature and up-regulate NK1.1, they acquire the ability to secrete IFN-gamma. Finally, the Tec family tyrosine kinase Itk is necessary for optimal NK1.1 up-regulation and hence final maturation of NK T cells. The itk(-/-) mice also display a progressive decrease in NK T cells in older animals, suggesting a further role in peripheral maintenance.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.169.5.2397</identifier><identifier>PMID: 12193707</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Animals ; Antigens - biosynthesis ; Antigens, CD - biosynthesis ; Antigens, Ly ; Antigens, Surface - biosynthesis ; CD4 Antigens - biosynthesis ; CD8 Antigens - biosynthesis ; Cell Differentiation - genetics ; Cell Differentiation - immunology ; Cell Division - genetics ; Cell Division - immunology ; Cytokines - biosynthesis ; Cytokines - physiology ; Immunophenotyping ; Injections, Intravenous ; Integrin alpha2 ; Interleukin-7 - pharmacology ; Killer Cells, Natural - cytology ; Killer Cells, Natural - enzymology ; Killer Cells, Natural - immunology ; Killer Cells, Natural - metabolism ; Lectins, C-Type ; Lymphocyte Transfusion ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; NK Cell Lectin-Like Receptor Subfamily B ; Protein Biosynthesis ; Protein-Tyrosine Kinases - deficiency ; Protein-Tyrosine Kinases - genetics ; Protein-Tyrosine Kinases - physiology ; Proteins ; Stem Cell Transplantation ; Stem Cells - immunology ; Stem Cells - metabolism ; T-Lymphocyte Subsets - cytology ; T-Lymphocyte Subsets - enzymology ; T-Lymphocyte Subsets - immunology ; T-Lymphocyte Subsets - metabolism ; Time Factors</subject><ispartof>The Journal of immunology (1950), 2002-09, Vol.169 (5), p.2397-2406</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-ab05c0602a5968721213666ba8cab141af4cb60b6054c05ce4530d8cf028916e3</citedby><cites>FETCH-LOGICAL-c409t-ab05c0602a5968721213666ba8cab141af4cb60b6054c05ce4530d8cf028916e3</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/12193707$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gadue, Paul</creatorcontrib><creatorcontrib>Stein, Paul L</creatorcontrib><title>NK T Cell Precursors Exhibit Differential Cytokine Regulation and Require Itk for Efficient Maturation</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>NK T cells are a lymphocyte lineage that is selected by CD1d and is characterized by the ability to rapidly secrete large amounts of both IFN-gamma and IL-4 after TCR stimulation. Using reactivity to CD1d tetramers to define presumptive NK T cells, several NK T cell progenitor populations were characterized based upon NK marker expression and CD4 vs CD8 expression. The earliest populations were found to be negative for NK markers and could proliferate to IL-7, while mature NK T cells did not. The NK1.1(-) NK T cell progenitors were capable of up-regulating NK1.1 when transferred in vivo. Upon stimulation, the NK1.1(-) populations secrete IL-4, but little IFN-gamma. As the cells mature and up-regulate NK1.1, they acquire the ability to secrete IFN-gamma. Finally, the Tec family tyrosine kinase Itk is necessary for optimal NK1.1 up-regulation and hence final maturation of NK T cells. The itk(-/-) mice also display a progressive decrease in NK T cells in older animals, suggesting a further role in peripheral maintenance.</description><subject>Animals</subject><subject>Antigens - biosynthesis</subject><subject>Antigens, CD - biosynthesis</subject><subject>Antigens, Ly</subject><subject>Antigens, Surface - biosynthesis</subject><subject>CD4 Antigens - biosynthesis</subject><subject>CD8 Antigens - biosynthesis</subject><subject>Cell Differentiation - genetics</subject><subject>Cell Differentiation - immunology</subject><subject>Cell Division - genetics</subject><subject>Cell Division - immunology</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - physiology</subject><subject>Immunophenotyping</subject><subject>Injections, Intravenous</subject><subject>Integrin alpha2</subject><subject>Interleukin-7 - pharmacology</subject><subject>Killer Cells, Natural - cytology</subject><subject>Killer Cells, Natural - enzymology</subject><subject>Killer Cells, Natural - immunology</subject><subject>Killer Cells, Natural - metabolism</subject><subject>Lectins, C-Type</subject><subject>Lymphocyte Transfusion</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>NK Cell Lectin-Like Receptor Subfamily B</subject><subject>Protein Biosynthesis</subject><subject>Protein-Tyrosine Kinases - deficiency</subject><subject>Protein-Tyrosine Kinases - genetics</subject><subject>Protein-Tyrosine Kinases - physiology</subject><subject>Proteins</subject><subject>Stem Cell Transplantation</subject><subject>Stem Cells - immunology</subject><subject>Stem Cells - metabolism</subject><subject>T-Lymphocyte Subsets - cytology</subject><subject>T-Lymphocyte Subsets - enzymology</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocyte Subsets - metabolism</subject><subject>Time Factors</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkUtLAzEUhYMoWqu_QJCsdDX1JpNJZpZS6wOfiK5DJk1sdB42maH6701tRXdC4BL4zrmPg9ABgREDVpy8urrum7YaEV6MshFNC7GBBiTLIOEc-CYaAFCaEMHFDtoN4RUAOFC2jXYIJUUqQAyQvbvGT3hsqgo_eKN7H1of8ORj5krX4TNnrfGm6Zyq8Piza99cY_Cjeekr1bm2waqZxu-8d97gq-4N29bjibVOuyjCt6rr_Te4h7asqoLZX9chej6fPI0vk5v7i6vx6U2iGRRdokrI9HJIlRU8FzTOmXLOS5VrVRJGlGW65BBfxnREDctSmObaAs0Lwk06REcr33ffznsTOlm7oON2qjFtH6SgQEXB2L8gyZmAZfshSleg9m0I3lj57l2t_KckIJc5yJ8cZMxBZnKZQ1Qdru37sjbTX8368BE4XgEz9zJbxPPJUKuqijiRi8Xij9UXnwaTZA</recordid><startdate>20020901</startdate><enddate>20020901</enddate><creator>Gadue, Paul</creator><creator>Stein, Paul L</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>20020901</creationdate><title>NK T Cell Precursors Exhibit Differential Cytokine Regulation and Require Itk for Efficient Maturation</title><author>Gadue, Paul ; Stein, Paul L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-ab05c0602a5968721213666ba8cab141af4cb60b6054c05ce4530d8cf028916e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Antigens - biosynthesis</topic><topic>Antigens, CD - biosynthesis</topic><topic>Antigens, Ly</topic><topic>Antigens, Surface - biosynthesis</topic><topic>CD4 Antigens - biosynthesis</topic><topic>CD8 Antigens - biosynthesis</topic><topic>Cell Differentiation - genetics</topic><topic>Cell Differentiation - immunology</topic><topic>Cell Division - genetics</topic><topic>Cell Division - immunology</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - physiology</topic><topic>Immunophenotyping</topic><topic>Injections, Intravenous</topic><topic>Integrin alpha2</topic><topic>Interleukin-7 - pharmacology</topic><topic>Killer Cells, Natural - cytology</topic><topic>Killer Cells, Natural - enzymology</topic><topic>Killer Cells, Natural - immunology</topic><topic>Killer Cells, Natural - metabolism</topic><topic>Lectins, C-Type</topic><topic>Lymphocyte Transfusion</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>NK Cell Lectin-Like Receptor Subfamily B</topic><topic>Protein Biosynthesis</topic><topic>Protein-Tyrosine Kinases - deficiency</topic><topic>Protein-Tyrosine Kinases - genetics</topic><topic>Protein-Tyrosine Kinases - physiology</topic><topic>Proteins</topic><topic>Stem Cell Transplantation</topic><topic>Stem Cells - immunology</topic><topic>Stem Cells - metabolism</topic><topic>T-Lymphocyte Subsets - cytology</topic><topic>T-Lymphocyte Subsets - enzymology</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocyte Subsets - metabolism</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gadue, Paul</creatorcontrib><creatorcontrib>Stein, Paul L</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>Gadue, Paul</au><au>Stein, Paul L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NK T Cell Precursors Exhibit Differential Cytokine Regulation and Require Itk for Efficient Maturation</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2002-09-01</date><risdate>2002</risdate><volume>169</volume><issue>5</issue><spage>2397</spage><epage>2406</epage><pages>2397-2406</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>NK T cells are a lymphocyte lineage that is selected by CD1d and is characterized by the ability to rapidly secrete large amounts of both IFN-gamma and IL-4 after TCR stimulation. Using reactivity to CD1d tetramers to define presumptive NK T cells, several NK T cell progenitor populations were characterized based upon NK marker expression and CD4 vs CD8 expression. The earliest populations were found to be negative for NK markers and could proliferate to IL-7, while mature NK T cells did not. The NK1.1(-) NK T cell progenitors were capable of up-regulating NK1.1 when transferred in vivo. Upon stimulation, the NK1.1(-) populations secrete IL-4, but little IFN-gamma. As the cells mature and up-regulate NK1.1, they acquire the ability to secrete IFN-gamma. Finally, the Tec family tyrosine kinase Itk is necessary for optimal NK1.1 up-regulation and hence final maturation of NK T cells. The itk(-/-) mice also display a progressive decrease in NK T cells in older animals, suggesting a further role in peripheral maintenance.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>12193707</pmid><doi>10.4049/jimmunol.169.5.2397</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1767 |
ispartof | The Journal of immunology (1950), 2002-09, Vol.169 (5), p.2397-2406 |
issn | 0022-1767 1550-6606 |
language | eng |
recordid | cdi_proquest_miscellaneous_72027944 |
source | Free E-Journal (出版社公開部分のみ) |
subjects | Animals Antigens - biosynthesis Antigens, CD - biosynthesis Antigens, Ly Antigens, Surface - biosynthesis CD4 Antigens - biosynthesis CD8 Antigens - biosynthesis Cell Differentiation - genetics Cell Differentiation - immunology Cell Division - genetics Cell Division - immunology Cytokines - biosynthesis Cytokines - physiology Immunophenotyping Injections, Intravenous Integrin alpha2 Interleukin-7 - pharmacology Killer Cells, Natural - cytology Killer Cells, Natural - enzymology Killer Cells, Natural - immunology Killer Cells, Natural - metabolism Lectins, C-Type Lymphocyte Transfusion Mice Mice, Inbred C57BL Mice, Knockout NK Cell Lectin-Like Receptor Subfamily B Protein Biosynthesis Protein-Tyrosine Kinases - deficiency Protein-Tyrosine Kinases - genetics Protein-Tyrosine Kinases - physiology Proteins Stem Cell Transplantation Stem Cells - immunology Stem Cells - metabolism T-Lymphocyte Subsets - cytology T-Lymphocyte Subsets - enzymology T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism Time Factors |
title | NK T Cell Precursors Exhibit Differential Cytokine Regulation and Require Itk for Efficient Maturation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T03%3A46%3A26IST&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=NK%20T%20Cell%20Precursors%20Exhibit%20Differential%20Cytokine%20Regulation%20and%20Require%20Itk%20for%20Efficient%20Maturation&rft.jtitle=The%20Journal%20of%20immunology%20(1950)&rft.au=Gadue,%20Paul&rft.date=2002-09-01&rft.volume=169&rft.issue=5&rft.spage=2397&rft.epage=2406&rft.pages=2397-2406&rft.issn=0022-1767&rft.eissn=1550-6606&rft_id=info:doi/10.4049/jimmunol.169.5.2397&rft_dat=%3Cproquest_cross%3E18470121%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c409t-ab05c0602a5968721213666ba8cab141af4cb60b6054c05ce4530d8cf028916e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=18470121&rft_id=info:pmid/12193707&rfr_iscdi=true |