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Regulation of dendritic cell maturation and function by Bruton's tyrosine kinase via IL-10 and Stat3.


ABSTRACT: Btk plays crucial roles in the differentiation and activation of B and myeloid cells. Despite drastic reductions of other Ig isotypes, paradoxically high IgE responses have been known in btk mutant mice. Here we show that btk(-/-) dendritic cells exhibit a more mature phenotype and a stronger in vitro and in vivo T cell-stimulatory ability than wild-type cells. Increased IgE responses were induced by adoptive transfer of btk(-/-) dendritic cells into mice. Consistent with the stronger T cell-stimulatory ability of btk(-/-) dendritic cells, btk(-/-) mice exhibited enhanced inflammation in Th2-driven asthma and Th1-driven contact sensitivity experiments. These negative regulatory functions of Btk in dendritic cells appear to be mediated mainly through autocrine secretion of IL-10 and subsequent activation of Stat3.

SUBMITTER: Kawakami Y 

PROVIDER: S-EPMC1325006 | biostudies-literature | 2006 Jan

REPOSITORIES: biostudies-literature

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Regulation of dendritic cell maturation and function by Bruton's tyrosine kinase via IL-10 and Stat3.

Kawakami Yuko Y   Inagaki Naoki N   Salek-Ardakani Shahram S   Kitaura Jiro J   Tanaka Hiroyuki H   Nagao Koichi K   Kawakami Yu Y   Xiao Wenbin W   Nagai Hiroichi H   Croft Michael M   Kawakami Toshiaki T  

Proceedings of the National Academy of Sciences of the United States of America 20051221 1


Btk plays crucial roles in the differentiation and activation of B and myeloid cells. Despite drastic reductions of other Ig isotypes, paradoxically high IgE responses have been known in btk mutant mice. Here we show that btk(-/-) dendritic cells exhibit a more mature phenotype and a stronger in vitro and in vivo T cell-stimulatory ability than wild-type cells. Increased IgE responses were induced by adoptive transfer of btk(-/-) dendritic cells into mice. Consistent with the stronger T cell-sti  ...[more]

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