Regulation of IL-17 expression by the developmental pathway of CD4 T cells in the thymus

Mol Immunol. 2010 Mar;47(6):1262-8. doi: 10.1016/j.molimm.2009.12.010. Epub 2010 Jan 18.

Abstract

CD4 T cells selected by MHC class II expressing thymocytes (T-CD4 T cells) have distinct effector functions compared to that of epithelial cell-selected CD4 T cells (E-CD4 T cells). T-CD4 T cells produce both Th1 and Th2 effector cytokines immediately after stimulation and also express IL-4 in addition to IFN-gamma under the Th1 differentiation condition. In the present study, we investigated the capability of T-CD4 T cells to become IL-17-producing cells. We found that T-CD4 T cells express reduced IL-17 under Th17-inducing conditions. T-CD4 T cells express very low levels of receptor for TGF-beta and IL-21 that are essential to induce IL-17 expression. In addition, the induction of RORgammat, a key transcription factor for IL-17 gene expression, was compromised in T-CD4 T cells under Th17 skewing conditions and ectopic expression of RORgammat restored IL-17 expression. The defect of IL-17 and RORgammat expression in T-CD4 T cells is cell intrinsic and not due to effects of a secreted factor. Thus, the developmental pathway of CD4 T cells in the thymus plays a critical role in controlling an immune response by suppressing the generation of the Th17 lineage.

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / cytology*
  • CD4-Positive T-Lymphocytes / immunology*
  • Cell Separation
  • Gene Expression Regulation*
  • Humans
  • Interleukin-17 / genetics*
  • Interleukin-17 / metabolism*
  • Interleukin-4 / deficiency
  • Interleukin-4 / metabolism
  • Mice
  • Mice, Transgenic
  • Nuclear Proteins / genetics
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / genetics
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / metabolism
  • Receptors, Interleukin-21 / genetics
  • Receptors, Interleukin-21 / metabolism
  • Receptors, Transforming Growth Factor beta / genetics
  • Receptors, Transforming Growth Factor beta / metabolism
  • STAT6 Transcription Factor / deficiency
  • STAT6 Transcription Factor / metabolism
  • Thymus Gland / cytology*
  • Trans-Activators / genetics

Substances

  • Interleukin-17
  • MHC class II transactivator protein
  • Nuclear Proteins
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • Receptors, Interleukin-21
  • Receptors, Transforming Growth Factor beta
  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Trans-Activators
  • Interleukin-4