Qian Yinhua, Zhu Jinguo, He Yanwei, Qin Haocheng, Qian Pingkang, Sun Bingfeng, Huang Haoqiang, Kuang Chen, Yang Quan, Ou Yuxi, Sun Rong, Xu Feng, Wang Xianwen, Luo Zhiwen, Wang Qing
Department of Orthopedics, Kunshan Hospital of Chinese Medicine,Kunshan Hospital Affiliated to Nanjing University of Chinese Medicine, No.388 Zuchongzhi South Road, Kunshan, Jiangsu, 215300, China.
Department of Orthopedics, Nantong Tongzhou Hospital of Traditional Chinese Medicine, No.8 Jianshe Road, Tongzhou, Jiangsu, 226300, China.
Adv Sci (Weinh). 2025 Sep;12(34):e09883. doi: 10.1002/advs.202509883. Epub 2025 Jun 19.
Osteoporosis significantly impairs tendon-bone healing, increasing the risk of rotator cuff tears and postoperative retearing. Tendon stem/progenitor cells (TSPCs) are vital for tendon repair, with their stemness crucial to healing outcomes. This study investigated the role of CD248 in regulating TSPC stemness and assessed the therapeutic potential of si-CD248-loaded liposomes in promoting tendon-bone healing under osteoporotic conditions. Single-cell RNA sequencing (scRNA-seq) identified increased TSPC populations, particularly a unique subcluster, TSPC-0, with elevated CD248 expression in osteoporotic tendon samples. CD248 TSPCs displayed reduced proliferation, increased apoptosis, and impaired migration, driven by altered FAK-JAK-STAT1 signaling. si-CD248-loaded liposomes were formulated and characterized, demonstrating efficacy in inhibiting CD248 expression, restoring TSPC stemness, and promoting tendon-bone healing. In osteoporotic mice, liposome treatment significantly enhanced tissue regeneration, improving histological scores, collagen organization, and biomechanical properties. This study reveals that elevated CD248 expression negatively impacts TSPC stemness and impairs healing under osteoporotic conditions. Targeting CD248 using si-CD248-loaded liposomes effectively restores TSPC regenerative potential, representing a promising therapeutic strategy to enhance tendon-bone healing in osteoporotic patients.
骨质疏松症会显著损害肌腱-骨愈合,增加肩袖撕裂和术后再撕裂的风险。肌腱干/祖细胞(TSPCs)对肌腱修复至关重要,其干性对愈合结果起着关键作用。本研究调查了CD248在调节TSPC干性中的作用,并评估了负载si-CD248的脂质体在促进骨质疏松条件下肌腱-骨愈合方面的治疗潜力。单细胞RNA测序(scRNA-seq)发现骨质疏松肌腱样本中TSPC群体增加,特别是一个独特的亚群TSPC-0,其CD248表达升高。CD248 TSPCs表现出增殖减少、凋亡增加和迁移受损,这是由FAK-JAK-STAT1信号改变驱动的。制备并表征了负载si-CD248的脂质体,证明其在抑制CD248表达、恢复TSPC干性和促进肌腱-骨愈合方面的功效。在骨质疏松小鼠中,脂质体治疗显著增强了组织再生,改善了组织学评分、胶原组织和生物力学性能。本研究表明,CD248表达升高对TSPC干性产生负面影响,并在骨质疏松条件下损害愈合。使用负载si-CD248的脂质体靶向CD248可有效恢复TSPC的再生潜力,这代表了一种有前景的治疗策略,可增强骨质疏松患者的肌腱-骨愈合。