PAQR11 modulates monocyte-to-macrophage differentiation and pathogenesis of rheumatoid arthritis

Immunology. 2021 May;163(1):60-73. doi: 10.1111/imm.13303. Epub 2021 Jan 24.

Abstract

During inflammation or tissue injury, pro-inflammatory mediators attract migratory monocytes to inflammatory sites and monocyte-to-macrophage differentiation occurs to activate macrophages. We report here that PAQR11, a member of the progesterone and AdipoQ receptor family, regulates monocyte-to-macrophage differentiation in vitro and in vivo. Paqr11 gene was highly induced during monocyte-to-macrophage differentiation. Knockdown or deletion of Paqr11 inhibited monocyte differentiation but had little effect on macrophage polarization. Mechanistically, PAQR11 promoted cell survival as apoptosis was increased by Paqr11 knockdown or deletion. Activation of the MAPK signalling pathway was involved in the regulatory role of PAQR11 on monocyte differentiation and cell survival. C/EBPβ regulated the expression of Paqr11 at the transcriptional level. In mice, deletion of Paqr11 gene alleviated progression of collagen-induced rheumatoid arthritis. Thus, these results provide strong evidence that PAQR11 has a function in monocyte-to-macrophage differentiation and such function is related to autoimmune disease in vivo.

Keywords: C/EBPβ; PAQR11; apoptosis; monocyte-to-macrophage differentiation; rheumatoid arthritis.

MeSH terms

  • Animals
  • Apoptosis
  • Arthritis, Experimental / genetics
  • Arthritis, Experimental / immunology
  • Arthritis, Experimental / metabolism*
  • Arthritis, Experimental / pathology
  • Arthritis, Rheumatoid / genetics
  • Arthritis, Rheumatoid / immunology
  • Arthritis, Rheumatoid / metabolism*
  • Arthritis, Rheumatoid / pathology
  • CCAAT-Enhancer-Binding Protein-beta / metabolism
  • Cell Differentiation*
  • Disease Progression
  • Gene Expression Regulation
  • HEK293 Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Macrophages / pathology
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism
  • Monocytes / immunology
  • Monocytes / metabolism*
  • Monocytes / pathology
  • Phosphorylation
  • Signal Transduction
  • THP-1 Cells

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • CEBPB protein, human
  • Cebpb protein, mouse
  • Intracellular Signaling Peptides and Proteins
  • MMD protein, human
  • Membrane Proteins
  • Mitogen-Activated Protein Kinases