Retinoic acid enhances Foxp3 induction indirectly by relieving inhibition from CD4+CD44hi Cells

Immunity. 2008 Nov 14;29(5):758-70. doi: 10.1016/j.immuni.2008.09.018.

Abstract

CD4(+)Foxp3(+) regulatory T (Treg) cells originate primarily from thymic differentiation, but conversion of mature T lymphocytes to Foxp3 positivity can be elicited by several means, including in vitro activation in the presence of TGF-beta. Retinoic acid (RA) increases TGF-beta-induced expression of Foxp3, through unknown molecular mechanisms. We showed here that, rather than enhancing TGF-beta signaling directly in naive CD4(+) T cells, RA negatively regulated an accompanying population of CD4(+) T cells with a CD44(hi) memory and effector phenotype. These memory cells actively inhibited the TGF-beta-induced conversion of naive CD4(+) T cells through the synthesis of a set of cytokines (IL-4, IL-21, IFN-gamma) whose expression was coordinately curtailed by RA. This indirect effect was evident in vivo and required the expression of the RA receptor alpha. Thus, cytokine-producing CD44(hi) cells actively restrain TGF-beta-mediated Foxp3 expression in naive T cells, and this balance can be shifted or fine-tuned by RA.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism
  • Forkhead Transcription Factors / immunology
  • Forkhead Transcription Factors / metabolism*
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Homeostasis
  • Hyaluronan Receptors / analysis
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism
  • Interleukin-4 / immunology
  • Interleukin-4 / metabolism
  • Interleukins / immunology
  • Interleukins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Receptors, Retinoic Acid / deficiency
  • Receptors, Retinoic Acid / immunology*
  • Receptors, Retinoic Acid / metabolism
  • Retinoic Acid Receptor alpha
  • Signal Transduction
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism
  • Transforming Growth Factor beta / immunology
  • Transforming Growth Factor beta / metabolism
  • Tretinoin / metabolism*

Substances

  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Hyaluronan Receptors
  • Interleukins
  • Rara protein, mouse
  • Receptors, Retinoic Acid
  • Retinoic Acid Receptor alpha
  • Transforming Growth Factor beta
  • Interleukin-4
  • Tretinoin
  • Interferon-gamma
  • interleukin-21

Associated data

  • GEO/GSE13306