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PAQR11 modulates monocyte‐to‐macrophage differentiation and pathogenesis of rheumatoid arthritis
Author(s) -
Lin Yijun,
Huang Meiqin,
Wang Shuo,
You Xue,
Zhang Lingling,
Chen Yan
Publication year - 2021
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1111/imm.13303
Subject(s) - monocyte , gene knockdown , macrophage , cellular differentiation , macrophage polarization , microbiology and biotechnology , mapk/erk pathway , inflammation , biology , immunology , cancer research , signal transduction , apoptosis , in vitro , gene , genetics
Summary 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 .