Generation of Foxp3+CD25- Regulatory T-Cell Precursors Requires c-Rel and IκBNS

Front Immunol. 2019 Jul 10:10:1583. doi: 10.3389/fimmu.2019.01583. eCollection 2019.

Abstract

Next to the classical developmental route, in which first CD25 and subsequently Foxp3 are induced to generate thymic regulatory T (Treg) cells, an alternative route has been described. This alternative route is characterized by reciprocal induction of Foxp3 and CD25, with CD25 induction being required to rescue developing Treg cells from Foxp3-induced apoptosis. NF-κB has been demonstrated to be crucial for the development of thymic Treg cells via the classical route. However, its impact on the alternative route is poorly characterized. Using single and double deficient mice for key regulators of the classical route, c-Rel and IκBNS, we here demonstrate that NF-κB is essential for the generation of alternative CD25-Foxp3+ precursors, as well. Thus, c-Rel and IκBNS govern both routes of thymic Treg cell development.

Keywords: NF-κB; cell differentiation; common γ-chain cytokines; regulatory T cell; thymus; transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cells, Cultured
  • Forkhead Transcription Factors / metabolism
  • I-kappa B Proteins / genetics
  • I-kappa B Proteins / metabolism*
  • Interleukin-2 Receptor alpha Subunit / metabolism
  • Lymphocyte Activation
  • Mice
  • Mice, Knockout
  • Proto-Oncogene Proteins c-rel / genetics
  • Proto-Oncogene Proteins c-rel / metabolism*
  • T-Lymphocytes, Regulatory / physiology*
  • Thymocytes / physiology*

Substances

  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • I-kappa B Proteins
  • Interleukin-2 Receptor alpha Subunit
  • Nfkbid protein, mouse
  • Proto-Oncogene Proteins c-rel