Department of Oral and Maxillofacial Surgery, Erasmus MC, University Medical Center Rotterdam, the Netherlands.
Dr. Rolf Schwiete Research Unit for Osteoarthritis, Orthopaedic University Hospital Friedrichsheim, Frankfurt, Germany.
Cartilage. 2021 Dec;13(2_suppl):1229S-1236S. doi: 10.1177/1947603520961170. Epub 2020 Sep 29.
To evaluate if 3 peptides derived from the cartilage oligomeric matrix protein (COMP), which wounded zones of cartilage secrete into synovial fluid, possess biological activity and might therefore be involved in the regulation of specific aspects of joint regeneration.
The 3 peptides were produced by chemical synthesis and then tested for known functions of the COMP C-terminal domain from which they derive, and which are involved in osteoarthritis: transforming growth factor-β (TGF-β) signaling, vascular homeostasis, and inflammation. . None of the peptides affected the gene expression of in osteochondral progenitor cells ( > 0.05). We observed no effects on the vascularization potential of endothelial cells ( > 0.05). In cultured synovium explants, no differences on the expression of catabolic enzymes or proinflammatory cytokines were found when peptides were added ( > 0.05).
The 3 peptides tested do not regulate TGF-β signaling, angiogenesis and vascular tube formation, or synovial inflammation and therefore most likely do not play a major role in the disease process.
评估软骨寡聚基质蛋白(COMP)的 3 个肽段是否具有生物学活性,这些肽段来源于软骨损伤区域分泌到滑液中的 COMP C 端结构域,而该结构域可能参与关节再生的特定方面的调控。
通过化学合成生产这 3 个肽段,然后对其进行测试,以验证它们是否具有已知的 COMP C 端结构域功能,这些功能与骨关节炎有关:转化生长因子-β(TGF-β)信号、血管稳态和炎症。。这 3 个肽段均未影响骨软骨祖细胞的基因表达(> 0.05)。我们观察到内皮细胞的血管生成潜力没有差异(> 0.05)。在培养的滑膜外植体中,加入肽段时,细胞外基质分解代谢酶或促炎细胞因子的表达没有差异(> 0.05)。
测试的 3 个肽段不调节 TGF-β信号、血管生成和血管管形成或滑膜炎症,因此它们不太可能在疾病过程中发挥主要作用。