Department of Pediatrics McGovern Medical School University of Texas, 6431 Fannin MSB 3.122b, Houston, TX 77030, USA; School of Dentistry at The University of Texas Health Science Center at Houston (UTHealth), Houston, TX 77030, USA.
Department of Pediatrics McGovern Medical School University of Texas, 6431 Fannin MSB 3.122b, Houston, TX 77030, USA.
Matrix Biol. 2023 May;119:101-111. doi: 10.1016/j.matbio.2023.03.008. Epub 2023 Mar 30.
Cartilage oligomeric matrix protein (COMP), an extracellular matrix protein, has been shown to enhance proliferation and mechanical integrity in the matrix, supporting functions of the growth plate and articular cartilage. Mutations in COMP cause pseudoachondroplasia (PSACH), a severe dwarfing condition associated with premature joint degeneration and significant lifelong joint pain. The MT (mutant)-COMP mouse mimics PSACH with decreased limb growth, early joint degeneration and pain. Ablation of endoplasmic reticulum stress CHOP signaling eliminated pain and prevented joint degeneration. The health effects of mutant COMP are discussed in relation to cellular/chondrocyte stress in the growth plate, articular cartilage and nearby tissues, and the implications for therapeutic approaches. There are many similarities between osteoarthritis and mutant-COMP protein-induced joint degeneration, suggesting that the relevance of findings in the joints may extend beyond PSACH to idiopathic primary OA.
软骨寡聚基质蛋白(COMP)是一种细胞外基质蛋白,已被证明能增强基质的增殖和机械完整性,支持生长板和关节软骨的功能。COMP 突变导致假性软骨发育不全(PSACH),这是一种严重的侏儒症,与过早的关节退化和严重的终身关节疼痛有关。MT(突变)-COMP 小鼠表现出肢体生长减少、早期关节退化和疼痛,与 PSACH 相似。内质网应激 CHOP 信号的消融消除了疼痛并防止了关节退化。本文讨论了突变型 COMP 对生长板、关节软骨和附近组织中细胞/软骨细胞应激的健康影响,以及对治疗方法的影响。骨关节炎和突变型 COMP 蛋白诱导的关节退化之间有许多相似之处,这表明关节中的发现的相关性可能不仅限于 PSACH,还可能扩展到特发性原发性 OA。