可注射的纤维软骨形成核心可增强大鼠肩袖模型的骨肌腱愈合能力

Yuhao Yuan, Yiyang Mao, Buhua Sun, Can Chen
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引用次数: 0

摘要

背景:手术修复肩袖(RC)撕裂后,由于骨肌腱(BT)止点再生有限,撕裂的肌腱愈合不理想,直至大结节。这种情况激发了对新的干预措施的需求,以加强在RC修复部位的BT愈合。目的:将成纤维细胞生长因子18 (FGF18)系在脱细胞纤维软骨基质微颗粒(AFM-MPs)上制备可注射的纤维软骨形成核,并评价其对BT愈合的效果。研究设计:实验室对照研究。方法:我们从猪RC插入处获取正常纤维软骨组织,然后将其脱细胞,然后微粉化,用于制造AFM-MPs。将胶原结合域融合到FGF18的n端,合成重组FGF18 (CBD-FGF18),将其与AFM-MPs的胶原纤维结合,制备可注射的纤维软骨形成核心(CBD-FGF18@AFM-MPs)。在体外研究CBD-FGF18@AFM-MPs对骨髓间充质干细胞活力和成软骨分化的影响后,我们确定了CBD-FGF18@AFM-MPs对大鼠RC撕裂模型BT愈合的作用。选取80只RC损伤的Sprague-Dawley大鼠,随机分为4组:生理盐水注射(对照组)、AFM-MPs注射、天然FGF18@AFM-MPs注射和CBD-FGF18@AFM-MPs注射。术后4周和8周,采集的RC标本通过显微计算机断层扫描、组织学染色和力学测试进行评估。结果:CBD-FGF18@AFM-MPs具有较强的体外仿生能力,适合细胞生长和增殖,具有较强的促软骨形成作用。体内微计算机断层扫描结果显示,CBD-FGF18@AFM-MPs组新生骨形成明显多于其他3组,骨重塑明显优于其他3组。组织学上,在术后4周和8周,CBD-FGF18@AFM-MPs组BT插入的连续性最好,胶原排列规则,纤维软骨再生广泛。重要的是,在术后8周,CBD-FGF18@AFM-MPs组的RC试件表现出最高的破坏载荷和刚度。结论:可注射纤维软骨形成核心为促进RC愈合提供了一种新的生物干预手段。临床意义:可注射纤维软骨形成核心可能是手术修复RC撕裂的一种新的补充治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Injectable Fibrocartilage-Forming Cores Enhance Bone-Tendon Healing in a Rat Rotator Cuff Model
Background:After surgical repair of rotator cuff (RC) tears, the torn tendon heals unsatisfactorily to the greater tuberosity owing to limited regeneration of the bone-tendon (BT) insertion. This situation motivates the need for new interventions to enhance BT healing in the RC repair site.Purpose:To develop injectable fibrocartilage-forming cores by tethering fibroblast growth factor 18 (FGF18) on acellular fibrocartilage matrix microparticles (AFM-MPs) and evaluate their efficacy on BT healing.Study Design:Controlled laboratory study.Methods:We harvested normal fibrocartilage tissue from the porcine RC insertion, after which it was decellularized and then micronized for fabricating AFM-MPs. The collagen-binding domain was fused into the N-terminus of FGF18 to synthesize recombinant FGF18 (CBD-FGF18), which was tethered to the collagen fibers of AFM-MPs to prepare the injectable fibrocartilage-forming cores (CBD-FGF18@AFM-MPs). After examining the influence of the CBD-FGF18@AFM-MPs on the viability and chondrogenic differentiation of bone marrow mesenchymal stem cells in vitro, we determined the function of the CBD-FGF18@AFM-MPs on BT healing in a rat RC tear model. A total of 80 Sprague-Dawley rats with RC injuries were randomly assigned to 4 supplemental treatments during RC repair: saline injection (control group), AFM-MPs injection, natural FGF18@AFM-MPs injection, and CBD-FGF18@AFM-MPs injection. At 4 and 8 weeks postoperatively, the harvested RC specimens were evaluated via micro–computed tomography, histologic staining, and mechanical testing.Results:In vitro, the CBD-FGF18@AFM-MPs were highly biomimetic, suitable for cell growth and proliferation, and superior in stimulating chondrogenesis. In vivo micro–computed tomography results showed that the CBD-FGF18@AFM-MPs group had significantly more new bone formation and better bone remodeling than the other 3 groups. Histologically, at 4 and 8 weeks postoperatively, the CBD-FGF18@AFM-MPs group had the best continuity of the BT insertion with regular collagen alignment and extensive fibrocartilage regeneration. Importantly, at 8 weeks postoperatively, the RC specimens from the CBD-FGF18@AFM-MPs group presented the highest failure load and stiffness.Conclusion:The injectable fibrocartilage-forming cores provide a new biological intervention to promote RC healing.Clinical Relevance:The injectable fibrocartilage-forming cores may be a new complementary treatment for surgical repair of RC tears.
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