Immunoregulatory properties of the cytokine IL-34

Cell Mol Life Sci. 2017 Jul;74(14):2569-2586. doi: 10.1007/s00018-017-2482-4. Epub 2017 Mar 3.

Abstract

Interleukin-34 is a cytokine with only partially understood functions, described for the first time in 2008. Although IL-34 shares very little homology with CSF-1 (CSF1, M-CSF), they share a common receptor CSF-1R (CSF-1R) and IL-34 has also two distinct receptors (PTP-ζ) and CD138 (syndecan-1). To make the situation more complex, IL-34 has also been shown as pairing with CSF-1 to form a heterodimer. Until now, studies have demonstrated that this cytokine is released by some tissues that differ to those where CSF-1 is expressed and is involved in the differentiation and survival of macrophages, monocytes, and dendritic cells in response to inflammation. The involvement of IL-34 has been shown in areas as diverse as neuronal protection, autoimmune diseases, infection, cancer, and transplantation. Our recent work has demonstrated a new and possible therapeutic role for IL-34 as a Foxp3+ Treg-secreted cytokine mediator of transplant tolerance. In this review, we recapitulate most recent findings on IL-34 and its controversial effects on immune responses and address its immunoregulatory properties and the potential of targeting this cytokine in human.

Keywords: CSF-1(M-CSF); Immune tolerance; Ischemia reperfusion; Macrophages; Osteopetrosis; Tregs.

Publication types

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

MeSH terms

  • Animals
  • Clinical Trials as Topic
  • Humans
  • Immunomodulation*
  • Interleukins / metabolism*
  • Macrophage Colony-Stimulating Factor / metabolism
  • Models, Biological
  • Molecular Targeted Therapy

Substances

  • Interleukins
  • Macrophage Colony-Stimulating Factor