IL-21 inhibits IFN-gamma production in developing Th1 cells through the repression of Eomesodermin expression

J Immunol. 2006 Sep 15;177(6):3721-7. doi: 10.4049/jimmunol.177.6.3721.

Abstract

Exposure of naive Th cell precursors (Thp) to IL-21 inhibits IFN-gamma production from developing Th1 cells. The inhibition of IFN-gamma seen in IL-21-treated Thp cells is specific as the expression of other Th1 cytokines is unaffected. Recently, it has been reported that Eomesodermin (Eomes), a member of the T-box gene family, is expressed in developing CD8+ T cells and plays an important role in regulating IFN-gamma production and cytolytic effector function. In this study, we show that Eomes mRNA and protein are also expressed in developing Th1 cells, and exposure of naive Thp cells to IL-21 results in a decrease in Eomes expression. Moreover, the repression of Eomes expression by IL-21 is not due to an indirect effect of IL-21 on the expression of IFN-gamma or STAT4 and is independent of STAT1 and T-bet expression. Finally, we show that ectopic expression of Eomes prevents the inhibition of IFN-gamma production from IL-21-treated Thp cells. Taken together, these results demonstrate that Eomes plays a role in regulating IFN-gamma production in CD4+ T cells and IL-21 inhibits IFN-gamma production in developing Th1 cells through the repression of Eomes expression.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / immunology*
  • Cells, Cultured
  • Down-Regulation / immunology
  • Gene Expression Regulation / immunology
  • Interferon-gamma / antagonists & inhibitors*
  • Interferon-gamma / biosynthesis*
  • Interferon-gamma / deficiency
  • Interleukins / physiology*
  • Mesoderm / cytology
  • Mesoderm / immunology
  • Mesoderm / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • RNA, Messenger / metabolism
  • Repressor Proteins / physiology
  • Stem Cells / cytology
  • Stem Cells / immunology
  • Stem Cells / metabolism
  • T-Box Domain Proteins / antagonists & inhibitors*
  • T-Box Domain Proteins / biosynthesis*
  • T-Box Domain Proteins / physiology
  • Th1 Cells / cytology
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism*
  • Transcription Factors / physiology

Substances

  • Eomes protein, mouse
  • Interleukins
  • RNA, Messenger
  • Repressor Proteins
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Transcription Factors
  • Interferon-gamma
  • interleukin-21