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Foxo3 Promotes the Differentiation and Function of Follicular Helper T Cells.

Cell reports (2020-05-14)
Haiyu Qi, Dan Tian, Mingyang Li, Chunpan Zhang, Hua Jin, Liwei Liu, Xinyan Zhao, Linlin Ma, Weijia Zhao, Qing Ge, Ting Duan, Dong Zhang
RESUMO

Follicular helper T cells (Tfhs) are essential for germinal center (GC) B cell maturation and antibody development. However, the intrinsic mechanisms that regulate Tfh differentiation are largely unknown. Here, we demonstrate that the frequencies of Tfhs and GC B cells, as well as interleukin-21 (IL-21) and anti-ovalbumin (OVA) antibodies, are markedly decreased in forkhead box O3 (Foxo3) knockout mice immunized with OVA. Using mixed bone marrow chimeras and lymphocyte-repopulated Rag1-/- mice proves that wild-type (WT), but not Foxo3-deficient T cells provoke GC B cell maturation and antibody production. Deficiency of Foxo3 inhibits inducible T cell co-stimulator (ICOS)-induced Tfh differentiation. Chromatin immunoprecipitation assay results suggest that Foxo3 is able to bind to the IL-21 promoter and regulate IL-21 secretion. In conclusion, our study unveils a critical role of Foxo3 in the regulation of Tfh differentiation and IL-21 production. Modulating Foxo3 activity may be beneficial for enhancing or preventing antibody-mediated immune responses.

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Albumina, lyophilized powder, ≥98% (agarose gel electrophoresis)
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Neomicina, powder, BioReagent, suitable for cell culture
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Pepsina, tested according to Ph. Eur.