Department of Hand Surgery, China-Japan Union Hospital of Jilin University, Changchun, China.
School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Nat Commun. 2020 Jul 20;11(1):3642. doi: 10.1038/s41467-020-17378-z.
Carpal tunnel syndrome (CTS) is the most common peripheral nerve entrapment syndrome, affecting a large proportion of the general population. Genetic susceptibility has been implicated in CTS, but the causative genes remain elusive. Here, we report the identification of two mutations in cartilage oligomeric matrix protein (COMP) that segregate with CTS in two large families with or without multiple epiphyseal dysplasia (MED). Both mutations impair the secretion of COMP by tenocytes, but the mutation associated with MED also perturbs its secretion in chondrocytes. Further functional characterization of the CTS-specific mutation reveals similar histological and molecular changes of tendons/ligaments in patients' biopsies and the mouse models. The mutant COMP fails to oligomerize properly and is trapped in the ER, resulting in ER stress-induced unfolded protein response and cell death, leading to inflammation, progressive fibrosis and cell composition change in tendons/ligaments. The extracellular matrix (ECM) organization is also altered. Our studies uncover a previously unrecognized mechanism in CTS pathogenesis.
腕管综合征(CTS)是最常见的周围神经嵌压综合征,影响了很大一部分普通人群。遗传易感性与 CTS 有关,但致病基因仍不清楚。在这里,我们报告了软骨寡聚基质蛋白(COMP)中的两个突变的鉴定,这两个突变与两个有或没有多发性骨骺发育不良(MED)的大家族中的 CTS 分离。这两个突变都损害了成纤维细胞中 COMP 的分泌,但与 MED 相关的突变也扰乱了其在软骨细胞中的分泌。对 CTS 特异性突变的进一步功能特征分析揭示了患者活检和小鼠模型中肌腱/韧带的类似组织学和分子变化。突变的 COMP 不能正确寡聚化,被困在内质网中,导致内质网应激诱导的未折叠蛋白反应和细胞死亡,导致炎症、进行性纤维化和肌腱/韧带中的细胞成分改变。细胞外基质(ECM)的组织也发生了改变。我们的研究揭示了 CTS 发病机制中的一个以前未被认识的机制。