4.8 Article

Notch directly regulates Gata3 expression during T helper 2 cell differentiation

Journal

IMMUNITY
Volume 27, Issue 1, Pages 100-110

Publisher

CELL PRESS
DOI: 10.1016/j.immuni.2007.04.018

Keywords

-

Categories

Funding

  1. NCI NIH HHS [R01 CA092433, R01 CA092433-05, P01 CA119070, P01 CA119070-01A19001, P01 CA119070-020003] Funding Source: Medline
  2. NIAID NIH HHS [R01 AI047833-09, R01 AI047833] Funding Source: Medline
  3. NIGMS NIH HHS [T32 GM007229, T32GM007229] Funding Source: Medline

Ask authors/readers for more resources

Notch signaling plays multiple roles to direct diverse decisions regarding cell fate during T cell development. During helper T (Th) cell differentiation, Notch is involved in generating optimal Th2 cell responses. Here, we present data investigating how Notch mediates Th2 cell differentiation. Notch showed a CD4+ T cell intrinsic role in promoting IL-4 expression that required GATA-3. In the absence of Notch signals, Gata3 expression was markedly diminished. Introduction of an activated allele of Notchl into CD4+ T cells led to the specific and direct upregulation of a developmentally regulated Gata3 transcript that included the exon 1a sequences. Furthermore, Notch acted in parallel with GATA-3 to synergistically activate IL-4 expression. Together, these data implicate Gata3 as a direct transcriptional Notch target that acts in concert with Notch signaling to generate optimal Th2 cell responses.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available