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TGF-? induces the expression of the adaptor Ndfip1 to silence IL-4 production during iTreg cell differentiation.


ABSTRACT: Mice deficient in the adaptor Ndfip1 develop inflammation at sites of environmental antigen exposure. We show here that such mice had fewer inducible regulatory T cells (iT(reg) cells). In vitro, Ndfip1-deficient T cells expressed normal amounts of the transcription factor Foxp3 during the first 48 h of iT(reg) cell differentiation; however, this expression was not sustained. Abortive Foxp3 expression was caused by production of interleukin 4 (IL-4) by Ndfip1(-/-) cells. We found that Ndfip1 expression was transiently upregulated during iT(reg) cell differentiation in a manner dependent on transforming growth factor-? (TGF-?). Once expressed, Ndfip1 promoted degradation of the transcription factor JunB mediated by the E3 ubiquitin ligase Itch, thus preventing IL-4 production. On the basis of our data, we propose that TGF-? signaling induces Ndfip1 expression to silence IL-4 production, thus permitting iT(reg) cell differentiation.

SUBMITTER: Beal AM 

PROVIDER: S-EPMC3542978 | biostudies-literature | 2011 Nov

REPOSITORIES: biostudies-literature

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TGF-β induces the expression of the adaptor Ndfip1 to silence IL-4 production during iTreg cell differentiation.

Beal Allison M AM   Ramos-Hernández Natalia N   Riling Chris R CR   Nowelsky Erin A EA   Oliver Paula M PM  

Nature immunology 20111113 1


Mice deficient in the adaptor Ndfip1 develop inflammation at sites of environmental antigen exposure. We show here that such mice had fewer inducible regulatory T cells (iT(reg) cells). In vitro, Ndfip1-deficient T cells expressed normal amounts of the transcription factor Foxp3 during the first 48 h of iT(reg) cell differentiation; however, this expression was not sustained. Abortive Foxp3 expression was caused by production of interleukin 4 (IL-4) by Ndfip1(-/-) cells. We found that Ndfip1 exp  ...[more]

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