Activin A Promotes the TGF-β-Induced Conversion of CD4+CD25− T Cells into Foxp3+ Induced Regulatory T Cells

Samuel Huber(Universität Hamburg), Felix R. Stahl(Universität Hamburg), Jörg Schrader(Universität Hamburg), Stefan Lüth(Universität Hamburg), Katrin Presser(Universität Hamburg), Antonella Carambia(Universität Hamburg), Richard A. Flavell(Howard Hughes Medical Institute), Sabine Werner(Board of the Swiss Federal Institutes of Technology), Manfred Blessing(Leipzig University), Johannes Herkel(Universität Hamburg), Christoph Schramm(Universität Hamburg)
The Journal of Immunology
April 1, 2009
Cited by 108Open Access
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Abstract

TGF-beta induces the conversion of CD4(+)CD25(-) T cells into CD4(+)CD25(+)Foxp3(+) regulatory T cells (Treg). Activin A is a pleiotropic TGF-beta family member and is expressed in response to inflammatory signals. In this study, we report on the effects of activin A on the conversion of CD4(+)CD25(-) T cells into Foxp3-expressing induced Treg (iTreg). Activin A was able to promote the conversion of CD4(+)CD25(-) T cells into iTreg in a dose-dependent manner in vitro. Activin A together with TGF-beta1 had synergistic effects on the rate of iTreg conversion in vitro. Intact TGF-beta1 signaling seemed to be essential for the effects of activin A on iTreg generation because cells overexpressing a dominant negative TGF-beta type II receptor could not be converted by activin A in vitro. In vivo, the frequency of peripheral, but not central, Treg was increased in transgenic mice with elevated activin A serum levels and the in vivo conversion rate of CD4(+)CD25(-) T cells into Foxp3-expressing iTreg was increased as compared with wild type mice. These data suggest a role for activin A as a promoter of the TGF-beta dependent conversion of CD4(+)CD25(-) T cells into iTreg in vitro and in vivo. Therefore, besides promoting inflammation, activin A may contribute to the regulation of inflammation via the expansion of peripheral Treg.


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