Analysis of proteins released from osteoarthritic cartilage by compressive loading

In osteoarthritis (OA), synovial pathology may be induced by proteins released from degenerated cartilage. This study was conducted to identify the proteins released from OA cartilage. OA cartilage was obtained from OA knees at macroscopically preserved areas (PRES) and degenerated areas (DEG), whil...

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Veröffentlicht in:Scientific reports 2023-10, Vol.13 (1), p.18292-18292, Article 18292
Hauptverfasser: Tsuno, Hirotaka, Tanaka, Nobuho, Naito, Masashi, Ohashi, Satoru, Iwasawa, Mitsuyasu, Kadoguchi, Tomoyasu, Mitomi, Hiroyuki, Matsui, Toshihiro, Furukawa, Hiroshi, Fukui, Naoshi
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Sprache:eng
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Zusammenfassung:In osteoarthritis (OA), synovial pathology may be induced by proteins released from degenerated cartilage. This study was conducted to identify the proteins released from OA cartilage. OA cartilage was obtained from OA knees at macroscopically preserved areas (PRES) and degenerated areas (DEG), while control cartilage (CONT) was collected from non-arthritic knees. Released proteins were obtained from these cartilage samples by repeatedly applying compressive loading, which simulated loading on cartilage in vivo. The released proteins were analyzed comprehensively by antibody array analyses and a quantitative proteomic analysis. For several proteins, the exact amounts released were determined by Luminex assays. The amount of active TGF-β that was released was determined by an assay using genetically-engineered HEK cells. The results of the antibody array and proteomic analyses revealed that various biologically active proteins are released from OA cartilage, particularly from DEG, by loading. The Luminex assay confirmed that several alarmins, complement proteins C3a and C5a, and several angiogenic proteins including FGF-1, FGF-2 and VEGF-A were released in greater amounts from DEG than from CONT. The HEK cell assay indicated that active TGF-β was released from DEG at biologically significant levels. These findings may be helpful in understanding the pathology of OA.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-023-45472-x