Stat5a regulates T helper cell differentiation by several distinct mechanisms

Blood. 2001 Apr 15;97(8):2358-65. doi: 10.1182/blood.v97.8.2358.

Abstract

We have previously shown that CD4(+) T cell-mediated allergic inflammation is diminished in signal transducer and activator of transcription (Stat)5a-deficient (Stat5a(-/-)) mice. To determine whether Stat5a regulates T helper cell differentiation, we studied T helper (Th)1 and Th2 cell differentiation of Stat5a(-/-)CD4(+) T cells at single-cell levels. First, Th2 cell differentiation from antigen-stimulated splenocytes was significantly decreased in Stat5a(-/-) mice as compared with that in wild-type mice. Further, Th2 cell differentiation was also impaired in Stat5a(-/-) mice even when purified CD4(+) T cells were stimulated with anti-CD3 plus anti-CD28 antibodies in the presence of interleukin-4. Moreover, the retrovirus-mediated gene expression of Stat5a in Stat5a(-/-)CD4(+) T cells restored the Th2 cell differentiation at the similar levels to that in wild-type CD4(+) T cells. In addition, interleukin-4 normally phosphorylated Stat6 in CD4(+) T cells from Stat5a(-/-) mice. Second, the development of CD4(+)CD25(+) immunoregulatory T cells was impaired in Stat5a(-/-) mice, as indicated by a significant decrease in the number of CD4(+)CD25(+) T cells in Stat5a(-/-) mice. Furthermore, the depletion of CD4(+)CD25(+) T cells from wild-type splenocytes significantly decreased Th2 cell differentiation but increased Th1 cell differentiation, whereas the depletion of CD4(+)CD25(+) T cells from Stat5a(-/-) splenocytes had no significant effect on the Th1 and Th2 cell differentiation. Together, these results indicate that the intrinsic expression of Stat5a in CD4(+) T cells is required for Th2 cell differentiation and that Stat5a is involved in the development of CD4(+)CD25(+) immunoregulatory T cells that modulate T helper cell differentiation toward Th2 cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4 Antigens / analysis
  • Cell Cycle
  • Cell Differentiation
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / physiology*
  • Gene Expression
  • Interleukin-4 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Milk Proteins*
  • Receptors, Interleukin-2 / analysis
  • Recombinant Fusion Proteins / physiology
  • STAT5 Transcription Factor
  • STAT6 Transcription Factor
  • Specific Pathogen-Free Organisms
  • Spleen / cytology
  • Th1 Cells / cytology*
  • Th1 Cells / metabolism
  • Th2 Cells / cytology*
  • Th2 Cells / metabolism
  • Trans-Activators / deficiency
  • Trans-Activators / metabolism
  • Trans-Activators / physiology*

Substances

  • CD4 Antigens
  • DNA-Binding Proteins
  • Milk Proteins
  • Receptors, Interleukin-2
  • Recombinant Fusion Proteins
  • STAT5 Transcription Factor
  • STAT6 Transcription Factor
  • Stat5a protein, mouse
  • Stat6 protein, mouse
  • Trans-Activators
  • Interleukin-4