Department of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, 730030, Gansu, China.
Department of Spine Surgery, Honghui Hospital, Xi'an Jiaotong University, Xi'an, 710054, Shaanxi, China.
J Orthop Surg Res. 2024 Sep 28;19(1):610. doi: 10.1186/s13018-024-05089-w.
Osteoporosis (OP) is a systemic bone disease characterized by reduced bone mass and deterioration of bone microstructure, leading to increased bone fragility. Platelets can take up and release cytokines, and a high platelet count has been associated with low bone density. Obesity is strongly associated with OP, and adipose tissue can influence platelet function by secreting adipokines. However, the biological relationship between these factors remains unclear.
We conducted differential analysis to identify OP platelet-related plasma proteins. And, making comprehensive analysis, including functional enrichment, protein-protein interaction network analysis, and Friends analysis. The key protein, Tetranectin (TNA/CLEC3B), was identified through screening. Then, we analyzed TNA's potential roles in osteogenic and adipogenic differentiation using multiple RNA-seq data sets and validated its effect on osteoclast differentiation and bone resorption function through in vitro experiments.
Six OP-platelet-related proteins were identified via differential analysis. Then, we screened the key protein TNA, which was found to be highly expressed in adipose tissue. RNA-seq data suggested that TNA may promote early osteoblast differentiation. In vitro experiments showed that knockdown of TNA expression significantly increased the expression of osteoclast markers, thereby promoting osteoclast differentiation and bone resorption.
We identified TNA as a secreted protein that inhibits osteoclast differentiation and bone resorption. While, it potentially promoted early osteoblast differentiation from bioinformatic results. TNA may play a role in bone metabolism through the adipose-bone axis.
骨质疏松症(OP)是一种以骨量减少和骨微观结构恶化为特征的系统性骨骼疾病,导致骨脆性增加。血小板可以摄取和释放细胞因子,血小板计数高与骨密度低有关。肥胖与 OP 强烈相关,脂肪组织可以通过分泌脂肪因子来影响血小板功能。然而,这些因素之间的生物学关系尚不清楚。
我们进行了差异分析,以确定与 OP 血小板相关的血浆蛋白。然后,通过综合分析,包括功能富集、蛋白质-蛋白质相互作用网络分析和 Friends 分析,筛选出关键蛋白 Tetranectin(TNA/CLEC3B)。然后,我们使用多个 RNA-seq 数据集分析了 TNA 在成骨和脂肪生成分化中的潜在作用,并通过体外实验验证了其对破骨细胞分化和骨吸收功能的影响。
通过差异分析鉴定了 6 种与 OP 血小板相关的蛋白质。然后,我们筛选出关键蛋白 TNA,发现其在脂肪组织中高表达。RNA-seq 数据表明,TNA 可能促进早期成骨细胞分化。体外实验表明,TNA 表达的下调显著增加了破骨细胞标志物的表达,从而促进破骨细胞分化和骨吸收。
我们确定 TNA 是一种抑制破骨细胞分化和骨吸收的分泌蛋白。然而,它可能通过生物信息学结果促进早期成骨细胞分化。TNA 可能通过脂肪-骨骼轴在骨骼代谢中发挥作用。