Yang Jun, Chen Xiaolin, Wu Yueshu, Xu Gang, Qu Xiaochen
Department of Orthopaedics, First Affiliated Hospital of Dalian Medical University, Dalian, PR China.
Department of Orthopedic Surgery, The Second Affiliated Hospital of Chongqing Medical University, No. 76, Linjiang Road, Chongqing, 400010, Yuzhong District, PR China.
J Orthop Surg Res. 2024 Jul 16;19(1):407. doi: 10.1186/s13018-024-04915-5.
Oncostatin M (OSM) is involved in the regulation of osteogenic differentiation and has a major role in the development of heterotopic ossification. The role of OSM in osteogenic differentiation of tendon-derived stem cells (TDSCs) and its mechanism have not been reported. This study aim to investigate the role of OSM in osteogenic differentiation of TDSCs and study the mechanism.
TDSCs were differentiated in osteogenic differentiation medium for 7 days. Recombinant OSM was added to the osteogenic differentiation medium for 7 and 14 days. The effect of Janus kinase 2 (JAK2) inhibitor AZD1480 and signal transducer and activator of transcription 3 (STAT3) inhibitor stattic in the presence of recombinant OSM on osteogenic differentiation of TDSCs was examined after differentiation for 7 and 14 days. Alkaline phosphatase and alizarin red staining were used to assess the effects on early and mid-stage osteogenic differentiation, respectively. Western blotting and qPCR were used to assess the expression of receptor and signalling pathway-related proteins and osteogenic marker genes, respectively.
TDSCs were successfully induced to differentiate into osteoblasts. Recombinant OSM promoted osteogenic differentiation of TDSCs to early and mid-stages. After addition of AZD1480 or stattic, decreased alkaline phosphatase and alizarin red staining were observed in the early and mid-stages of osteogenic differentiation. Additionally, decreased expression of receptor and pathway-related proteins, and osteogenic genes was found by western blotting and qPCR, respectively.
OSM promotes osteogenic differentiation of TDSCs and the JAK2/STAT3 signalling pathway plays an important role.
抑瘤素M(OSM)参与成骨分化的调控,在异位骨化的发生发展中起主要作用。OSM在肌腱衍生干细胞(TDSCs)成骨分化中的作用及其机制尚未见报道。本研究旨在探讨OSM在TDSCs成骨分化中的作用并研究其机制。
将TDSCs在成骨分化培养基中培养7天。在成骨分化培养基中添加重组OSM,培养7天和14天。在分化7天和14天后,检测Janus激酶2(JAK2)抑制剂AZD1480和信号转导及转录激活因子3(STAT3)抑制剂stattic在重组OSM存在下对TDSCs成骨分化的影响。分别用碱性磷酸酶和茜素红染色评估对早期和中期成骨分化的影响。分别用蛋白质免疫印迹法和定量聚合酶链反应(qPCR)评估受体及信号通路相关蛋白和成骨标记基因的表达。
TDSCs成功诱导分化为成骨细胞。重组OSM促进TDSCs成骨分化至早期和中期。添加AZD1480或stattic后,在成骨分化的早期和中期观察到碱性磷酸酶和茜素红染色减少。此外,分别通过蛋白质免疫印迹法和qPCR发现受体及通路相关蛋白和成骨基因的表达降低。
OSM促进TDSCs的成骨分化,JAK2/STAT3信号通路起重要作用。