4.6 Article

Suppression of Th2 cell development by notch ligands Delta1 and Delta4

Journal

JOURNAL OF IMMUNOLOGY
Volume 180, Issue 3, Pages 1655-1661

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.180.3.1655

Keywords

-

Categories

Funding

  1. NIAID NIH HHS [R01 AI053825-06, R01 AI053825-04, R01 AI053825-08, R01 AI053825-10, R01 AI053825-09, R01 AI053825-05, R01 AI053825-03, R01 AI053825-01, R01 AI053825, R01 AI053825-02, R01 AI053825-07, AI 53825] Funding Source: Medline

Ask authors/readers for more resources

Notch signaling plays important roles in Th cell activation. We show that in response to TLR ligation, dendritic cells up-regulate expression of Notch ligands Delta1 and Delta4 via a MyD88-dependent pathway. Expression of Delta1 or Delta4 by dendritic cells enhanced their ability to activate naive Th cells and promote Th1 cell development, and allowed them to strongly inhibit Th2 cell development. Promotion of Th1 cell development was dependent on IFN-gamma and T-bet expression by responding Th cells. However, the inhibition of Th2 cell development occurred independently of IFN-gamma or T-bet, and resulted from a block in IL-4-initiated commitment to the Th2 lineage. The promotion of Th1 cell development by Delta is not a reflection of the delivery of pro-Th1 instructional signal, but rather it is the result of a block in the downstream effects initiated by IL-4 signaling.

Authors

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

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available