Yuan Yuhao, Mao Yiyang, Sun Buhua, Chen Can
Department of Orthopedics, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
Am J Sports Med. 2025 Jan;53(1):66-79. doi: 10.1177/03635465241300138.
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.
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.
Controlled laboratory study.
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.
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.
The injectable fibrocartilage-forming cores provide a new biological intervention to promote RC healing.
The injectable fibrocartilage-forming cores may be a new complementary treatment for surgical repair of RC tears.
肩袖(RC)撕裂手术修复后,由于骨 - 肌腱(BT)附着处再生能力有限,撕裂的肌腱与大结节的愈合情况不尽人意。这种情况促使人们需要新的干预措施来促进RC修复部位的BT愈合。
通过将成纤维细胞生长因子18(FGF18) tethering在无细胞纤维软骨基质微粒(AFM - MPs)上,开发可注射的形成纤维软骨的核心,并评估它们对BT愈合的功效。
对照实验室研究。
我们从猪的RC附着处采集正常纤维软骨组织,将其脱细胞后再进行微粉化以制备AFM - MPs。将胶原结合结构域融合到FGF18的N端以合成重组FGF18(CBD - FGF18),将其 tethering到AFM - MPs的胶原纤维上以制备可注射的形成纤维软骨的核心(CBD - FGF18@AFM - MPs)。在体外研究了CBD - FGF18@AFM - MPs对骨髓间充质干细胞活力和软骨分化的影响后,我们在大鼠RC撕裂模型中确定了CBD - FGF18@AFM - MPs对BT愈合的作用。总共80只患有RC损伤的Sprague - Dawley大鼠在RC修复期间被随机分配到4种补充治疗组:注射生理盐水(对照组)、注射AFM - MPs、注射天然FGF18@AFM - MPs和注射CBD - FGF18@AFM - MPs。术后4周和8周,通过微计算机断层扫描、组织学染色和力学测试对采集的RC标本进行评估。
在体外,CBD - FGF18@AFM - MPs具有高度仿生特性,适合细胞生长和增殖,并且在刺激软骨形成方面更具优势。体内微计算机断层扫描结果显示,CBD - FGF18@AFM - MPs组比其他3组有明显更多的新骨形成和更好的骨重塑。组织学上,术后4周和8周,CBD - FGF18@AFM - MPs组的BT附着处连续性最佳,胶原排列规则,有广泛的纤维软骨再生。重要的是,术后8周,CBD - FGF18@AFM - MPs组的RC标本呈现出最高的破坏载荷和刚度。
可注射的形成纤维软骨的核心为促进RC愈合提供了一种新的生物干预措施。
可注射的形成纤维软骨的核心可能是RC撕裂手术修复的一种新的辅助治疗方法。