Journal
JOURNAL OF TRANSLATIONAL MEDICINE
Volume 19, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s12967-021-02823-4
Keywords
Osteoarthritis; Pirfenidone; Human fibroblast-like synoviocytes; Synovium; Fibrosis; Inflammation
Categories
Funding
- Natural Science Foundation of China [NSFC: 81672173, 82072448]
- Key Project for Science Research and Development of Shaanxi Province [2019ZDLSF03-07]
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The study found that PFD can inhibit the migration of FLSs, reduce the expression of COL1A1, alleviate synovial inflammation and fibrosis, and delay the progression of OA.
Background Osteoarthritis (OA) is a disease of the entire joint involving synovial fibrosis and inflammation. Pathological changes to the synovium can accelerate the progression of OA. Pirfenidone (PFD) is a potent anti-fibrotic drug with additional anti-inflammatory properties. However, the influence of PFD on OA is unknown. Methods Proliferation of human fibroblast-like synoviocytes (FLSs) after treatment with TGF-beta 1 or PFD was evaluated using a Cell Counting Kit-8 assay and their migration using a Transwell assay. The expression of fibrosis-related genes (COL1A1, TIMP-1, and ACTA-2) and those related to inflammation (IL-6 and TNF-alpha) was quantified by real-time quantitative PCR. The protein expression levels of COL1A1, alpha-SMA (coded by ACTA-2), IL-6 and TNF-alpha were measured by enzyme-linked immunosorbent assay. A rabbit model of OA was established and then PFD was administered by gavage. The expression of genes related to fibrosis (COL1A1, TIMP-1, and ADAM-12) and inflammation (IL-6 and TNF-alpha) was measured using RNA extracted from the synovium. Synovial tissue was examined histologically after staining with H&E, Masson's trichrome, and immunofluorescence. Synovitis scores, the volume fraction of collagen, and mean fluorescence intensity were calculated. Degeneration of articular cartilage was analyzed using a Safranin O-fast green stain and OARSI grading. Results The proliferation of FLSs was greatest when induced with 2.5 ng/ml TGF-beta 1 although it did not promote their migration. Therefore, 2.5 ng/ml TGF-beta 1 was used to stimulate the FLSs and evaluate the effects of PFD, which inhibited the migration of FLSs at concentrations as low as 1.0 mg/ml. PFD decreased the expression of COL1A1 while TGF-beta 1 increased both mRNA and protein expression levels of IL-6 but had no effect on alpha-SMA or TNF-alpha expression. PFD decreased mRNA expression levels of COL1A1, IL-6, and TNF-alpha in vivo. H&E staining and synovitis scores indicated that PFD reduced synovial inflammation, while Masson's trichrome and immunofluorescence staining suggested that PFD decreased synovial fibrosis. Safranin O-Fast Green staining and the OARSI scores demonstrated that PFD delayed the progression of OA. Conclusions PFD attenuated synovial fibrosis and inflammation, and postponed the progression of osteoarthritis in a modified Hulth model of OA in rabbits, which was related to its anti-fibrotic and anti-inflammatory properties.
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