Proteoglycan-4 is an essential regulator of synovial macrophage polarization and inflammatory macrophage joint infiltration

• Published in: Arthritis research & therapy 2021-09, Vol.23 (1), p.241-241, Article 241
• Main Authors: Qadri, Marwa, Jay, Gregory D, Zhang, Ling X, Schmidt, Tannin A, Totonchy, Jennifer, Elsaid, Khaled A
• Format: Article
• Language: English
• Subjects: Animals; Arthritis; Bone marrow; Bone-marrow-derived macrophages; Care and treatment; Cartilage; Collagen; Cytokines; Fibroblasts; Genotype & phenotype; Health aspects; Hyperplasia; Inflammation; Investigations; Macrophage Activation; Macrophages; Mice; Osteoarthritis; PRG4; Proteoglycans; Proteoglycans - genetics; Smooth muscle; Synovial hyperplasia; Synovial macrophages; Synovial Membrane; Synovial membranes; Tumor necrosis factor-TNF
• ISSN: 1478-6362; 1478-6354; 1478-6362
• DOI: 10.1186/s13075-021-02621-9

Synovial macrophages perform a multitude of functions that include clearance of cell debris and foreign bodies, tissue immune surveillance, and resolution of inflammation. The functional diversity of macrophages is enabled by distinct subpopulations that express unique surface markers. Proteoglycan-4 (PRG4) is an important regulator of synovial hyperplasia and fibrotic remodeling, and the involvement of macrophages in PRG4's synovial role is yet to be defined. Our objectives were to study the PRG4's importance to macrophage homeostatic regulation in the synovium and infiltration of pro-inflammatory macrophages in acute synovitis and investigate whether macrophages mediated synovial fibrosis in Prg4 gene-trap (Prg4 ) murine knee joints. Macrophage phenotyping in Prg4 and Prg4 joints was performed by flow cytometry using pan-macrophage markers, e.g., CD11b, F4/80, and surface markers of M1 macrophages (CD86) and M2 macrophages (CD206). Characterizations of the various macrophage subpopulations were performed in 2- and 6-month-old animals. The expression of inflammatory markers, IL-6, and iNOS in macrophages that are CD86+ and/or CD206+ was studied. The impact of Prg4 recombination on synovial macrophage populations of 2- and 6-month-old animals and infiltration of pro-inflammatory macrophages in response to a TLR2 agonist challenge was determined. Macrophages were depleted using liposomal clodronate and synovial membrane thickness, and the expression of fibrotic markers α-SMA, PLOD2, and collagen type I (COL-I) was assessed using immunohistochemistry. Total macrophages in Prg4 joints were higher than Prg4 joints (p