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Immunity ; 25(1): 93-104, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16860760

RESUMO

Mutations affecting the Tec kinases Itk and Rlk decrease T cell receptor-induced Ca(2+) mobilization and Erk kinase activation and impair both positive and negative thymic selection. Itk(-/-) and Rlk(-/-)Itk(-/-) mice also have decreased CD4:8 T cell ratios, suggestive of altered CD4:8 lineage commitment. Nonetheless, we find that CD8 single-positive (SP) thymocytes and peripheral CD8(+) T cells in these mice do not resemble conventional CD8(+) T cells. Instead, these cells express memory markers, rapidly produce interferon-gamma, and can be selected on hematopoietically derived cells, similar to MHC class Ib-restricted "innate-type" lymphocytes. Itk deficiency also greatly increases the number of cells selected by MHC class Ib. Expression of a hypersensitive Erk2 mutant partially corrects the CD8(+) T cell phenotypes in Itk(-/-) mice, arguing that altered signaling permits development of this innate-type CD8(+) cell population. Our results suggest that Tec kinases differentially regulate development of conventional versus nonconventional lymphocytes.


Assuntos
Linfócitos T CD8-Positivos/citologia , Linfócitos T CD8-Positivos/enzimologia , Diferenciação Celular , Linhagem da Célula , Proteínas Tirosina Quinases/deficiência , Animais , Linfócitos T CD8-Positivos/imunologia , Antígenos de Histocompatibilidade/metabolismo , Camundongos , Camundongos Knockout , Técnicas de Cultura de Órgãos , Fenótipo , Proteínas Tirosina Quinases/classificação , Proteínas Tirosina Quinases/genética , Proteínas Tirosina Quinases/metabolismo , Transdução de Sinais , Timo/citologia , Timo/imunologia , Timo/metabolismo , Fatores de Tempo
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