A novel role for reciprocal CD30-CD30L signaling in the cross-talk between natural killer and dendritic cells

Biol Chem. 2012 Jan;393(1-2):101-6. doi: 10.1515/BC-2011-213.

Abstract

The interplay between dendritic cells (DCs) and natural killer (NK) cells directs adaptive immune responses. The molecular basis of the cross-talk is largely undefined. Here, we provide evidence for a contribution of CD30 (TNFRSF8) and its ligand CD30L (TNFSF8) expressed on NK cells and DCs, respectively. We demonstrate that CD30-mediated engagement of CD30L induced cytokine secretion from immature DCs via the mitogen-activated protein kinase pathway. Moreover, CD30L engagement promoted differentiation to mature DCs. On the contrary, the engagement of CD30 on NK cells resulted in an NF-κB-dependent release of TNF-α/IFN-γ. These data uncover a novel and unexpected role for CD30/CD30L that contributes to proinflammatory immune responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD30 Ligand / biosynthesis
  • CD30 Ligand / metabolism*
  • Dendritic Cells / cytology
  • Dendritic Cells / metabolism*
  • Humans
  • Ki-1 Antigen / biosynthesis
  • Ki-1 Antigen / metabolism*
  • Killer Cells, Natural / cytology
  • Killer Cells, Natural / metabolism*
  • Signal Transduction*

Substances

  • CD30 Ligand
  • Ki-1 Antigen
  • TNFSF8 protein, human