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Cutting edge: CD28 and c-Rel-dependent pathways initiate regulatory T cell development

  • Kieng B. Vang
  • , Jianying Yang
  • , Antonio J. Pagán
  • , Lin Xi Li
  • , Junmei Wang
  • , Jonathan M. Green
  • , Amer A. Beg
  • , Michael A. Farrar

Research output: Contribution to journalArticlepeer-review

Abstract

Regulatory T cell (Treg) development proceeds via a two-step process in which naive CD4+ thymocytes are first converted into CD4 +CD25+CD122+GITR+Foxp3- Treg progenitors, followed by a second step in which IL-2 converts these Treg progenitors into CD4+Foxp3+ Tregs. The costimulatory molecule CD28 is required for efficient Treg development. However, the stage at which CD28 affects Treg development remains undefined. In this article, we demonstrate that Cd28-/- mice lack Treg progenitors. Furthermore, the P187YAP motif in the cytoplasmic tail of CD28, which links CD28 to Lck activation, is required for this process. In contrast, the Y 170MNM motif, which links CD28 to PI3K activation, is not required for Treg progenitor development. Finally, the CD28/Lck pathway was shown to activate the NF-κB family of transcription factors. We demonstrate that c-Rel, but not NF-κB1, promotes the development of Treg progenitors. Thus, a CD28/c-Rel-dependent pathway is involved in initiating Treg development.

Original languageEnglish
Pages (from-to)4074-4077
Number of pages4
JournalJournal of Immunology
Volume184
Issue number8
DOIs
StatePublished - Apr 15 2010

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