Cargando…

Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells

Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin α(E)β(7) discriminates distinct subsets of murine CD4(+) regulatory T cells. Use of this marker has now helped to unravel a fundamental dichotomy among regulatory T cells. α(E) (−)CD25(+)...

Descripción completa

Detalles Bibliográficos
Autores principales: Huehn, Jochen, Siegmund, Kerstin, Lehmann, Joachim C.U., Siewert, Christiane, Haubold, Uta, Feuerer, Markus, Debes, Gudrun F., Lauber, Joerg, Frey, Oliver, Przybylski, Grzegorz K., Niesner, Uwe, de la Rosa, Maurus, Schmidt, Christian A., Bräuer, Rolf, Buer, Jan, Scheffold, Alexander, Hamann, Alf
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211798/
https://www.ncbi.nlm.nih.gov/pubmed/14757740
http://dx.doi.org/10.1084/jem.20031562
_version_ 1782148556775227392
author Huehn, Jochen
Siegmund, Kerstin
Lehmann, Joachim C.U.
Siewert, Christiane
Haubold, Uta
Feuerer, Markus
Debes, Gudrun F.
Lauber, Joerg
Frey, Oliver
Przybylski, Grzegorz K.
Niesner, Uwe
de la Rosa, Maurus
Schmidt, Christian A.
Bräuer, Rolf
Buer, Jan
Scheffold, Alexander
Hamann, Alf
author_facet Huehn, Jochen
Siegmund, Kerstin
Lehmann, Joachim C.U.
Siewert, Christiane
Haubold, Uta
Feuerer, Markus
Debes, Gudrun F.
Lauber, Joerg
Frey, Oliver
Przybylski, Grzegorz K.
Niesner, Uwe
de la Rosa, Maurus
Schmidt, Christian A.
Bräuer, Rolf
Buer, Jan
Scheffold, Alexander
Hamann, Alf
author_sort Huehn, Jochen
collection PubMed
description Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin α(E)β(7) discriminates distinct subsets of murine CD4(+) regulatory T cells. Use of this marker has now helped to unravel a fundamental dichotomy among regulatory T cells. α(E) (−)CD25(+) cells expressed L-selectin and CCR7, enabling recirculation through lymphoid tissues. In contrast, α(E)-positive subsets (CD25(+) and CD25(−)) displayed an effector/memory phenotype expressing high levels of E/P-selectin–binding ligands, multiple adhesion molecules as well as receptors for inflammatory chemokines, allowing efficient migration into inflamed sites. Accordingly, α(E)-expressing cells were found to be the most potent suppressors of inflammatory processes in disease models such as antigen-induced arthritis.
format Text
id pubmed-2211798
institution National Center for Biotechnology Information
language English
publishDate 2004
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-22117982008-03-11 Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells Huehn, Jochen Siegmund, Kerstin Lehmann, Joachim C.U. Siewert, Christiane Haubold, Uta Feuerer, Markus Debes, Gudrun F. Lauber, Joerg Frey, Oliver Przybylski, Grzegorz K. Niesner, Uwe de la Rosa, Maurus Schmidt, Christian A. Bräuer, Rolf Buer, Jan Scheffold, Alexander Hamann, Alf J Exp Med Article Regulatory T cells (Tregs) fulfill a central role in immune regulation. We reported previously that the integrin α(E)β(7) discriminates distinct subsets of murine CD4(+) regulatory T cells. Use of this marker has now helped to unravel a fundamental dichotomy among regulatory T cells. α(E) (−)CD25(+) cells expressed L-selectin and CCR7, enabling recirculation through lymphoid tissues. In contrast, α(E)-positive subsets (CD25(+) and CD25(−)) displayed an effector/memory phenotype expressing high levels of E/P-selectin–binding ligands, multiple adhesion molecules as well as receptors for inflammatory chemokines, allowing efficient migration into inflamed sites. Accordingly, α(E)-expressing cells were found to be the most potent suppressors of inflammatory processes in disease models such as antigen-induced arthritis. The Rockefeller University Press 2004-02-02 /pmc/articles/PMC2211798/ /pubmed/14757740 http://dx.doi.org/10.1084/jem.20031562 Text en Copyright © 2004, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Huehn, Jochen
Siegmund, Kerstin
Lehmann, Joachim C.U.
Siewert, Christiane
Haubold, Uta
Feuerer, Markus
Debes, Gudrun F.
Lauber, Joerg
Frey, Oliver
Przybylski, Grzegorz K.
Niesner, Uwe
de la Rosa, Maurus
Schmidt, Christian A.
Bräuer, Rolf
Buer, Jan
Scheffold, Alexander
Hamann, Alf
Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells
title Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells
title_full Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells
title_fullStr Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells
title_full_unstemmed Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells
title_short Developmental Stage, Phenotype, and Migration Distinguish Naive- and Effector/Memory-like CD4(+) Regulatory T Cells
title_sort developmental stage, phenotype, and migration distinguish naive- and effector/memory-like cd4(+) regulatory t cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211798/
https://www.ncbi.nlm.nih.gov/pubmed/14757740
http://dx.doi.org/10.1084/jem.20031562
work_keys_str_mv AT huehnjochen developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT siegmundkerstin developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT lehmannjoachimcu developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT siewertchristiane developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT haubolduta developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT feuerermarkus developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT debesgudrunf developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT lauberjoerg developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT freyoliver developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT przybylskigrzegorzk developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT niesneruwe developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT delarosamaurus developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT schmidtchristiana developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT brauerrolf developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT buerjan developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT scheffoldalexander developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells
AT hamannalf developmentalstagephenotypeandmigrationdistinguishnaiveandeffectormemorylikecd4regulatorytcells