4.6 Article

Cutting Edge: CD28 and c-Rel-Dependent Pathways Initiate Regulatory T Cell Development

Journal

JOURNAL OF IMMUNOLOGY
Volume 184, Issue 8, Pages 4074-4077

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0903933

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Funding

  1. Pew Scholar Award
  2. Cancer Investigator Award
  3. Leukemia and Lymphoma Society Scholar award
  4. National Institutes of Health [AI061165, HL062683, AI059715, 2T32-AI07313]

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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 P(187)YAP motif in the cytoplasmic tail of CD28, which links CD28 to Lck activation, is required for this process. In contrast, the (YMNM)-M-170 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-kappa B family of transcription factors. We demonstrate that c-Rel, but not NF-kappa B1, promotes the development of Treg progenitors. Thus, a CD28/c-Rel-dependent pathway is involved in initiating Treg development. The Journal of Immunology, 2010, 184: 4074-4077.

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