Department of Orthopedics, the Second Affiliated Hospital, Xi'an Jiaotong University, No. 157 Xiwu Road, Xi'an 710004, China; Department of Orthopedics, the First Affiliated Hospital of Henan University of Science and Technology, Luoyang, Henan Province 471003, China.
Department of Orthopedics, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang, Henan Province 471009, China.
Int J Biol Macromol. 2021 Sep 30;187:892-902. doi: 10.1016/j.ijbiomac.2021.07.159. Epub 2021 Jul 28.
N-glycosylation is a major post-translational modification of proteins and involved in many diseases, however, the state and role of N-glycosylation in cartilage degeneration of osteonecrosis of femoral head (ONFH) remain unclear. The aim of this study is to identify the glycoproteins of ONFH hip cartilage. Cartilage tissues were collected from nine patients with ONFH and nine individuals with traumatic femoral neck fracture. Cartilage glycoproteins were identified by glycoproteomics based on LC-MS/MS. The differentially N-glycoproteins including glycosites were identified in ONFH and controls. A total of 408 N-glycoproteins with 444 N-glycosites were identified in ONFH and control cartilage. Among them, 104 N-glycoproteins with 130 N-glycosites were significantly differential in ONFH and control cartilage, which including matrix-remodeling-associated protein 5, prolow-density lipoprotein receptor-related protein 1, clusterin and lysosome-associated membrane glycoprotein 2. Gene Ontology analysis revealed the significantly differential glycoproteins mainly belonged to protein metabolic process, single-multicellular organism process, proteolysis, biological adhesion and cell adhesion. KEGG pathway and protein-protein interaction analysis suggested that the significantly differential glycoproteins were associated with PI3K-Akt signalling pathway, ECM-receptor interaction, protein processing in the endoplasmic reticulum and N-glycan biosynthesis. This information provides substantial insight into the role of protein glycosylation in the development of cartilage degeneration of ONFH patients.
N-糖基化是蛋白质的一种主要翻译后修饰,参与许多疾病的发生,但 N-糖基化在股骨头坏死(ONFH)软骨退变中的状态和作用尚不清楚。本研究旨在鉴定股骨头坏死髋关节软骨中的糖蛋白。从 9 例股骨头坏死患者和 9 例创伤性股骨颈骨折患者中收集软骨组织。通过基于 LC-MS/MS 的糖蛋白质组学鉴定软骨糖蛋白。在股骨头坏死和对照组中鉴定出差异 N-糖蛋白,包括糖基化位点。在股骨头坏死和对照软骨中鉴定出 408 种 N-糖蛋白,包含 444 个 N-糖基化位点。其中,104 种 N-糖蛋白,包括基质重塑相关蛋白 5、前低密度脂蛋白受体相关蛋白 1、载脂蛋白和溶酶体相关膜糖蛋白 2,在股骨头坏死和对照软骨中存在显著差异,这些蛋白主要参与蛋白质代谢过程、单细胞生物过程、蛋白水解、生物粘附和细胞粘附。GO 分析显示,差异糖蛋白主要属于蛋白质代谢过程、单细胞生物过程、蛋白水解、生物粘附和细胞粘附。KEGG 通路和蛋白质相互作用分析表明,差异糖蛋白与 PI3K-Akt 信号通路、ECM-受体相互作用、内质网蛋白加工和 N-聚糖生物合成有关。这些信息为蛋白质糖基化在股骨头坏死患者软骨退变中的作用提供了重要的见解。