Kang Simiao, Shi Xin, Chen Yong, Zhang Lin, Liu Quanbo, Lin Ziyang, Lu Hongbin, Pan Haile
Department of Sports Medicine and Joint Arthroplasty, Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Department of Sports Medicine, Xiangya Hospital, Central South University, Changsha, 410008, China.
Mater Today Bio. 2024 Sep 19;29:101258. doi: 10.1016/j.mtbio.2024.101258. eCollection 2024 Dec.
Traditional meniscectomy or suture for meniscal tear usually leads to failed self-healing, cartilage degeneration and worse osteoarthritis. The strategies that facilitate the healing process of torn meniscus and safeguard knee cartilage against degeneration will be promising for clinical therapy. The CD56 umbilical cord mesenchymal stem cells (UCSCs) (CD56UCSCs) were sorted from Wharton's jelly using flow cytometer. Then, the modified decellularized Wharton's Jelly hydrogel (DWJH) was combined with isolated CD56Exos from CD56UCSCs to fabricate DWJH/CD56Exos. The in vitro studies were performed to characterize the DWJ (decellularized Wharton's Jelly). The injectability and rheological properties were assessed by shear rate and frequency sweep analysis. The biocompatibility and chondrogenic differentiation inducibility of DWJH/CD56Exos were performed on human bone marrow mesenchymal stem cells (hBMSCs) and RAW 264.7 cells. The release dynamics was evaluated in vitro and in vivo experiments. As for the in vivo experiments, the operated rats that subjected to a 2 mm full-thickness longitudinal tear in right medial anterior meniscus were injected a single dose of DWJH/CD56Exos. At 4 and 8 weeks postoperatively, torn meniscus healing and articular cartilage degeneration were evaluated by hematoxylin and eosin (H&E), safranin O/fast green (SO&FG), and Sirius red staining. In in vitro experiments, the injectable DWJH/CD56Exos demonstrated excellent biocompatibility, exosome releasing efficiency, injectable property and chondrogenic inducibility. The results of in vivo experiments revealed that DWJH/CD56Exos degraded over time, promoted meniscal chondrogenesis, organized meniscal extracellular matrix remodeling, safeguard articular cartilage and inhibited secondary cartilage degeneration, which accelerated further facilitated torn meniscus healing. The novel injectable DWJH/CD56Exos promoted meniscal tear healing by promoting meniscal chondrogenesis, safeguarding articular cartilage, and inhibiting secondary cartilage degeneration.
传统的半月板切除术或半月板撕裂缝合术通常会导致自我愈合失败、软骨退变以及更严重的骨关节炎。促进撕裂半月板愈合过程并保护膝关节软骨免于退变的策略对临床治疗具有重要意义。使用流式细胞仪从脐带华通氏胶中分离出CD56脐带间充质干细胞(UCSCs)(CD56UCSCs)。然后,将改良的脱细胞华通氏胶水凝胶(DWJH)与从CD56UCSCs中分离出的CD56外泌体(CD56Exos)结合,制备出DWJH/CD56Exos。进行体外研究以表征脱细胞华通氏胶(DWJ)。通过剪切速率和频率扫描分析评估其可注射性和流变学特性。在人骨髓间充质干细胞(hBMSCs)和RAW 264.7细胞上进行DWJH/CD56Exos的生物相容性和软骨生成诱导性研究。通过体外和体内实验评估其释放动力学。对于体内实验,对右膝内侧前半月板造成2毫米全层纵向撕裂的手术大鼠注射单剂量的DWJH/CD56Exos。在术后4周和8周,通过苏木精和伊红(H&E)、番红O/固绿(SO&FG)和天狼星红染色评估撕裂半月板的愈合情况和关节软骨退变情况。在体外实验中,可注射的DWJH/CD56Exos表现出优异的生物相容性、外泌体释放效率、可注射性和软骨生成诱导性。体内实验结果显示,DWJH/CD56Exos随时间降解,促进半月板软骨生成,组织半月板细胞外基质重塑,保护关节软骨并抑制继发性软骨退变,进一步加速促进撕裂半月板的愈合。新型可注射的DWJH/CD56Exos通过促进半月板软骨生成、保护关节软骨和抑制继发性软骨退变来促进半月板撕裂的愈合。