Signaling Lymphocyte Activation Molecule Family 5 Enhances Autophagy and Fine-Tunes Cytokine Response in Monocyte-Derived Dendritic Cells via Stabilization of Interferon Regulatory Factor 8

Front Immunol. 2018 Jan 26:9:62. doi: 10.3389/fimmu.2018.00062. eCollection 2018.

Abstract

Signaling lymphocyte activation molecule family (SLAMF) receptors are essential regulators of innate and adaptive immune responses. The function of SLAMF5/CD84, a family member with almost ubiquitous expression within the hematopoietic lineage is poorly defined. In this article, we provide evidence that in human monocyte-derived dendritic cells (moDCs) SLAMF5 increases autophagy, a degradative pathway, which is highly active in dendritic cells (DCs) and plays a critical role in orchestration of the immune response. While investigating the underlying mechanism, we found that SLAMF5 inhibited proteolytic degradation of interferon regulatory factor 8 (IRF8) a master regulator of the autophagy process by a mechanism dependent on the E3-ubiquitin ligase tripartite motif-containing protein 21 (TRIM21). Furthermore, we demonstrate that SLAMF5 influences the ratio of CD1a+ cells in differentiating DCs and partakes in the regulation of IL-1β, IL-23, and IL-12 production in LPS/IFNγ-activated moDCs in a manner that is consistent with its effect on IRF8 stability. In summary, our experiments identified SLAMF5 as a novel cell surface receptor modulator of autophagy and revealed an unexpected link between the SLAMF and IRF8 signaling pathways, both implicated in multiple human pathologies.

Keywords: IL-12p70; IRF8; LPS/IFNγ; SLAMF5; TRIM21; autophagy; dendritic cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy* / drug effects
  • Cell Differentiation
  • Cytokines / metabolism*
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism*
  • Gene Expression Regulation
  • Gene Silencing
  • Humans
  • Interferon Regulatory Factors / metabolism*
  • Models, Biological
  • Proteasome Endopeptidase Complex / metabolism
  • Signal Transduction*
  • Signaling Lymphocytic Activation Molecule Family / genetics
  • Signaling Lymphocytic Activation Molecule Family / metabolism*
  • Sirolimus / pharmacology

Substances

  • CD84 protein, human
  • Cytokines
  • Interferon Regulatory Factors
  • Signaling Lymphocytic Activation Molecule Family
  • interferon regulatory factor-8
  • Proteasome Endopeptidase Complex
  • Sirolimus