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TGF-β specifies T FH versus T H 17 cell fates in murine CD4 + T cells through c-Maf
T follicular helper (T ) cells are essential for effective antibody responses, but deciphering the intrinsic wiring of mouse T cells has long been hampered by the lack of a reliable protocol for their generation in vitro. We report that transforming growth factor-β (TGF-β) induces robust expression...
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Published in: | Science immunology 2024-03, Vol.9 (93), p.eadd4818 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | T follicular helper (T
) cells are essential for effective antibody responses, but deciphering the intrinsic wiring of mouse T
cells has long been hampered by the lack of a reliable protocol for their generation in vitro. We report that transforming growth factor-β (TGF-β) induces robust expression of T
hallmark molecules CXCR5 and Bcl6 in activated mouse CD4
T cells in vitro. TGF-β-induced mouse CXCR5
T
cells are phenotypically, transcriptionally, and functionally similar to in vivo-generated T
cells and provide critical help to B cells. The study further reveals that TGF-β-induced CXCR5 expression is independent of Bcl6 but requires the transcription factor c-Maf. Classical TGF-β-containing T helper 17 (T
17)-inducing conditions also yield separate CXCR5
and IL-17A-producing cells, highlighting shared and distinct cell fate trajectories of T
and T
17 cells. We demonstrate that excess IL-2 in high-density T cell cultures interferes with the TGF-β-induced T
cell program, that T
and T
17 cells share a common developmental stage, and that c-Maf acts as a switch factor for T
versus T
17 cell fates in TGF-β-rich environments in vitro and in vivo. |
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ISSN: | 2470-9468 2470-9468 |
DOI: | 10.1126/sciimmunol.add4818 |