IL-33 enhances retinoic acid signaling on CD4+ T cells

Cytokine. 2016 Sep:85:120-2. doi: 10.1016/j.cyto.2016.06.016. Epub 2016 Jun 17.

Abstract

Several molecules have been described as CD4+ T cells differentiation modulators and among them retinoic acid (RA) and more recently, IL-33, have been studied. Due to the similarities in T helper cell skewing properties between RA and IL-33, we asked whether IL-33 intersects, directly or indirectly, the RA signaling pathway. Total CD4+ T cells from DR5-luciferase mice were activated in the presence of RA with or without IL-33, and RA signaling was visualized using ex vivo imaging. Our results demonstrate that IL-33 itself is able to trigger RA signaling on CD4+ T cells, which is highly increased when IL-33 is added in conjunction with RA. This study presents IL-33 as a potential player that may synergize with RA in controlling T cell differentiation, and suggests that IL-33 may be an attractive target in controlling T cell differentiation in vivo.

Keywords: CD4+ T cells differentiation; IL-33; Retinoic acid.

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / metabolism*
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Interleukin-33 / metabolism*
  • Mice
  • Signal Transduction / physiology*
  • Tretinoin / metabolism*

Substances

  • Il33 protein, mouse
  • Interleukin-33
  • Tretinoin