The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da FIOCRUZ (ARCA) |
Texto Completo: | https://www.arca.fiocruz.br/handle/icict/41052 |
Resumo: | Acesso aberto em 30/04/2020 - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118715/pdf/jem2040381.pdf |
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Maillard, Michel H.Almeida, Vinicius Cotta deTakeshima, FuminaoNguyen, Deanna D.Michetti, PierreNagler, CathrynBhan, Atul K.Snapper, Scott B.2020-04-30T19:54:52Z2020-04-30T19:54:52Z2007MAILLARD, Michel H. et al. The Wiskott-Aldrich syndrome protein is required for the function of CD4+CD25+Foxp3+ regulatory T. Journal of Experimental Medicine, v. 204, n. 3, p. 381-391, Feb. 2007.0022-1007https://www.arca.fiocruz.br/handle/icict/4105210.1084/jem.200613381540-9538Acesso aberto em 30/04/2020 - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118715/pdf/jem2040381.pdfMassachusetts General Hospital. Gastrointestinal Unit. Boston, MA, USA / Harvard Medical School. Department of Medicine. Boston, MA, USA / Lausanne University Hospital. Department of Medicine. Division of Gastroenterology and Hepatology. Lausanne, Switzerland.Massachusetts General Hospital. Gastrointestinal Unit. Boston, MA, USA / Harvard Medical School. Department of Medicine. Boston, MA, USA / Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Ultraestrutura e Biologia Celular. Rio de Janeiro, RJ, Brasil.Massachusetts General Hospital. Gastrointestinal Unit. Boston, MA, USA / Harvard Medical School. Department of Medicine. Boston, MA, USA.Massachusetts General Hospital. Gastrointestinal Unit. Boston, MA, USA / Harvard Medical School. Department of Medicine. Boston, MA, USA.Lausanne University Hospital. Department of Medicine. Division of Gastroenterology and Hepatology; Lausanne, Switzerland.. Massachusetts General Hospital. Division of Rheumatology. Boston, MA, USA / . Massachusetts General Hospital. Division of Allergy and Immunology. Boston, MA, USA / Harvard Medical School. Department of Medicine. Boston, MA, USA;Massachusetts General Hospital. Immunopathology Unit and the Center for the Study of Inflammatory Bowel Diseases. Boston, MA,USA / Harvard Medical Schoo. Department of Pathology. Boston, MA, USA.Massachusetts General Hospital. Gastrointestinal Unit. Boston, MA, USA / Harvard Medical School Department of Medicine. Boston, MA, USAThe Wiskott-Aldrich syndrome, a primary human immunodeficiency, results from defective expression of the hematopoietic-specific cytoskeletal regulator Wiskott-Aldrich syndrome protein (WASP). Because CD4(+)CD25(+)Foxp3(+) naturally occurring regulatory T (nTreg) cells control autoimmunity, we asked whether colitis in WASP knockout (WKO) mice is associated with aberrant development/function of nTreg cells. We show that WKO mice have decreased numbers of CD4(+)CD25(+)Foxp3(+) nTreg cells in both the thymus and peripheral lymphoid organs. Moreover, we demonstrate that WKO nTreg cells are markedly defective in both their ability to ameliorate the colitis induced by the transfer of CD45RB(hi) T cells and in functional suppression assays in vitro. Compared with wild-type (WT) nTreg cells, WKO nTreg cells show significantly impaired homing to both mucosal (mesenteric) and peripheral sites upon adoptive transfer into WT recipient mice. Suppression defects may be independent of antigen receptor-mediated actin rearrangement because both WT and WKO nTreg cells remodeled their actin cytoskeleton inefficiently upon T cell receptor stimulation. Preincubation of WKO nTreg cells with exogenous interleukin (IL)-2, combined with antigen receptor-mediated activation, substantially rescues the suppression defects. WKO nTreg cells are also defective in the secretion of the immunomodulatory cytokine IL-10. Overall, our data reveal a critical role for WASP in nTreg cell function and implicate nTreg cell dysfunction in the autoimmunity associated with WASP deficiency.engRockefeller University PressSíndrome de Wiskott-AldrichProteínaCélulas T reguladoras CD4+CD25+Foxp3+Wiskott-Aldrich syndromeProteinCD4+CD25+Foxp3+ regulatory T cellsThe Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cellsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; 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dc.title.pt_BR.fl_str_mv |
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells |
title |
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells |
spellingShingle |
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells Maillard, Michel H. Síndrome de Wiskott-Aldrich Proteína Células T reguladoras CD4+CD25+Foxp3+ Wiskott-Aldrich syndrome Protein CD4+CD25+Foxp3+ regulatory T cells |
title_short |
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells |
title_full |
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells |
title_fullStr |
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells |
title_full_unstemmed |
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells |
title_sort |
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells |
author |
Maillard, Michel H. |
author_facet |
Maillard, Michel H. Almeida, Vinicius Cotta de Takeshima, Fuminao Nguyen, Deanna D. Michetti, Pierre Nagler, Cathryn Bhan, Atul K. Snapper, Scott B. |
author_role |
author |
author2 |
Almeida, Vinicius Cotta de Takeshima, Fuminao Nguyen, Deanna D. Michetti, Pierre Nagler, Cathryn Bhan, Atul K. Snapper, Scott B. |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Maillard, Michel H. Almeida, Vinicius Cotta de Takeshima, Fuminao Nguyen, Deanna D. Michetti, Pierre Nagler, Cathryn Bhan, Atul K. Snapper, Scott B. |
dc.subject.other.pt_BR.fl_str_mv |
Síndrome de Wiskott-Aldrich Proteína Células T reguladoras CD4+CD25+Foxp3+ |
topic |
Síndrome de Wiskott-Aldrich Proteína Células T reguladoras CD4+CD25+Foxp3+ Wiskott-Aldrich syndrome Protein CD4+CD25+Foxp3+ regulatory T cells |
dc.subject.en.pt_BR.fl_str_mv |
Wiskott-Aldrich syndrome Protein CD4+CD25+Foxp3+ regulatory T cells |
description |
Acesso aberto em 30/04/2020 - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118715/pdf/jem2040381.pdf |
publishDate |
2007 |
dc.date.issued.fl_str_mv |
2007 |
dc.date.accessioned.fl_str_mv |
2020-04-30T19:54:52Z |
dc.date.available.fl_str_mv |
2020-04-30T19:54:52Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
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publishedVersion |
dc.identifier.citation.fl_str_mv |
MAILLARD, Michel H. et al. The Wiskott-Aldrich syndrome protein is required for the function of CD4+CD25+Foxp3+ regulatory T. Journal of Experimental Medicine, v. 204, n. 3, p. 381-391, Feb. 2007. |
dc.identifier.uri.fl_str_mv |
https://www.arca.fiocruz.br/handle/icict/41052 |
dc.identifier.issn.pt_BR.fl_str_mv |
0022-1007 |
dc.identifier.doi.none.fl_str_mv |
10.1084/jem.20061338 |
dc.identifier.eissn.none.fl_str_mv |
1540-9538 |
identifier_str_mv |
MAILLARD, Michel H. et al. The Wiskott-Aldrich syndrome protein is required for the function of CD4+CD25+Foxp3+ regulatory T. Journal of Experimental Medicine, v. 204, n. 3, p. 381-391, Feb. 2007. 0022-1007 10.1084/jem.20061338 1540-9538 |
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https://www.arca.fiocruz.br/handle/icict/41052 |
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eng |
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Rockefeller University Press |
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Rockefeller University Press |
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