Abstract
The transcription factor Tbet is critical for the differentiation of Th1 CD4 T cells and is associated with the induction of multiple autoimmune diseases, including experimental autoimmune encephalomyelitis (EAE). Herein, we demonstrate that Tbet suppresses IL-17A and Th17 differentiation both in vitro and in vivo in a cell-intrinsic manner, and that in fact, Tbet is not necessary for EAE induction. Moreover, we find that IFNγ inhibits the production of IL-17A and IL-17F in a STAT1-dependent, Tbet-independent manner. These findings illustrate multiple mechanisms utilized by developing Th1 cells to silence the Th17 program.
Keywords:
CD4 T cell; Experimental autoimmune encephalomyelitis; IFNγ; IL-17A; Tbet.
Copyright © 2013. Published by Elsevier B.V.
Publication types
-
Research Support, N.I.H., Extramural
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
CD4 Antigens / metabolism
-
Cell Differentiation / drug effects*
-
Cell Polarity / drug effects
-
Central Nervous System / pathology
-
Disease Models, Animal
-
Encephalomyelitis, Autoimmune, Experimental / immunology
-
Encephalomyelitis, Autoimmune, Experimental / pathology
-
Gene Expression Regulation / drug effects
-
Homeodomain Proteins / genetics
-
Interleukin-12 Subunit p40 / genetics
-
Interleukin-17 / metabolism
-
Interleukin-17 / pharmacology*
-
Interleukin-21
-
Interleukins / metabolism
-
Leukocyte Common Antigens / genetics
-
Mice
-
Mice, 129 Strain
-
Mice, Inbred C57BL
-
Mice, Transgenic
-
Nuclear Receptor Subfamily 1, Group F, Member 3 / metabolism
-
STAT1 Transcription Factor / genetics
-
T-Box Domain Proteins / genetics
-
T-Box Domain Proteins / metabolism*
-
Th17 Cells / drug effects*
Substances
-
CD4 Antigens
-
Homeodomain Proteins
-
Interleukin-12 Subunit p40
-
Interleukin-17
-
Interleukins
-
Nuclear Receptor Subfamily 1, Group F, Member 3
-
Rorc protein, mouse
-
STAT1 Transcription Factor
-
Stat1 protein, mouse
-
T-Box Domain Protein 2
-
T-Box Domain Proteins
-
RAG-1 protein
-
Leukocyte Common Antigens
-
Ptprc protein, mouse
-
Interleukin-21