Li Dijun, Jiu Jingwei, Liu Haifeng, Yan Xiaojun, Li Xiaoke, Yan Lei, Zhang Jing, Fan Zijuan, Li Songyan, Du Guangyuan, Li Jiao Jiao, Du Yanan, Liu Wei, Wang Bin
Department of Orthopaedic Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310006, China.
Department of Orthopedics, The Second Hospital of Shanxi Medical University, Taiyuan, 030001, China.
Bioact Mater. 2024 Jul 2;36:474-489. doi: 10.1016/j.bioactmat.2024.06.029. eCollection 2024 Jun.
Tendinopathy leads to low-grade tissue inflammation and chronic damage, which progresses due to pathological imbalance in angiogenesis. Reducing early pathological vascularization may be a new approach in helping to regenerate tendon tissue. Conventional stem cell therapy and tissue engineering scaffolds have not been highly effective at treating tendinopathy. In this study, tissue engineered stem cells (TSCs) generated using human umbilical cord mesenchymal stem cells (hUC-MSCs) were combined with microcarrier scaffolds to limit excessive vascularization in tendinopathy. By preventing VEGF receptor activation through their paracrine function, TSCs reduced angiogenesis and the proliferation of vascular endothelial cells. TSCs also decreased the inflammatory expression of tenocytes while promoting their anabolic and tenogenic characteristics. Furthermore, local injection of TSCs into rats with collagenase-induced tendinopathy substantially reduced early inflammation and vascularization. Mechanistically, transcriptome sequencing revealed that TSCs could reduce the progression of pathological angiogenesis in tendon tissue, attributed to Rap1-mediated vascular inhibition. TSCs may serve as a novel and practical approach for suppressing tendon vascularization, and provide a promising therapeutic agent for early-stage clinical tendinopathy.
肌腱病会导致低度组织炎症和慢性损伤,由于血管生成的病理失衡,这种损伤会不断进展。减少早期病理性血管生成可能是帮助肌腱组织再生的一种新方法。传统的干细胞疗法和组织工程支架在治疗肌腱病方面效果并不理想。在本研究中,将利用人脐带间充质干细胞(hUC-MSCs)生成的组织工程干细胞(TSCs)与微载体支架相结合,以限制肌腱病中的过度血管生成。通过其旁分泌功能阻止VEGF受体激活,TSCs减少了血管生成以及血管内皮细胞的增殖。TSCs还降低了肌腱细胞的炎症表达,同时促进了它们的合成代谢和肌腱生成特性。此外,将TSCs局部注射到胶原酶诱导的肌腱病大鼠体内,可显著减轻早期炎症和血管生成。从机制上讲,转录组测序显示TSCs可以减少肌腱组织中病理性血管生成的进展,这归因于Rap1介导的血管抑制。TSCs可能是一种抑制肌腱血管生成的新颖且实用的方法,并为早期临床肌腱病提供一种有前景的治疗药物。