含有 CD56+ 脐带间充质干细胞衍生外泌体的可注射脱细胞沃顿果冻水凝胶,用于半月板撕裂愈合和软骨保护

IF 8.7 1区 医学 Q1 ENGINEERING, BIOMEDICAL
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引用次数: 0

摘要

传统的半月板切除术或半月板撕裂缝合术通常会导致半月板自愈失败、软骨退化和骨关节炎恶化。促进半月板撕裂愈合和保护膝关节软骨不退化的策略将在临床治疗中大有可为。利用流式细胞仪从沃顿果冻中分拣出 CD56+ 脐带间充质干细胞(UCSCs)(CD56+UCSCs)。然后,将改良的脱细胞沃顿果冻水凝胶(DWJH)与从 CD56+UCSCs 分离出的 CD56+Exos 结合,制成 DWJH/CD56+Exos。体外研究对脱细胞沃顿果冻水凝胶(DWJ)进行了表征。通过剪切速率和频率扫描分析评估了注射性和流变特性。在人骨髓间充质干细胞(hBMSCs)和 RAW 264.7 细胞上对 DWJH/CD56+Exos 的生物相容性和软骨分化诱导性进行了研究。在体外和体内实验中对释放动态进行了评估。在体内实验方面,对右侧内侧前半月板2毫米全厚纵向撕裂的手术大鼠注射单剂量的DWJH/CD56+Exos。术后4周和8周,用苏木精和伊红(H&E)、安全素O/快绿(SO&FG)和天狼星红染色法评估半月板撕裂愈合和关节软骨退化情况。在体外实验中,注射用DWJH/CD56+外泌体表现出良好的生物相容性、外泌体释放效率、可注射性和软骨诱导性。体内实验结果表明,DWJH/CD56+Exos可随时间降解,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,抑制继发性软骨变性,进一步加速半月板撕裂愈合。新型注射剂DWJH/CD56+Exos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化,促进半月板撕裂愈合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Injectable decellularized Wharton's jelly hydrogel containing CD56+ umbilical cord mesenchymal stem cell-derived exosomes for meniscus tear healing and cartilage protection

Injectable decellularized Wharton's jelly hydrogel containing CD56+ umbilical cord mesenchymal stem cell-derived exosomes for meniscus tear healing and cartilage protection

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) (CD56+UCSCs) were sorted from Wharton's jelly using flow cytometer. Then, the modified decellularized Wharton's Jelly hydrogel (DWJH) was combined with isolated CD56+Exos from CD56+UCSCs to fabricate DWJH/CD56+Exos. 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/CD56+Exos 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/CD56+Exos. 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/CD56+Exos demonstrated excellent biocompatibility, exosome releasing efficiency, injectable property and chondrogenic inducibility. The results of in vivo experiments revealed that DWJH/CD56+Exos 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/CD56+Exos promoted meniscal tear healing by promoting meniscal chondrogenesis, safeguarding articular cartilage, and inhibiting secondary cartilage degeneration.

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来源期刊
CiteScore
8.30
自引率
4.90%
发文量
303
审稿时长
30 days
期刊介绍: Materials Today Bio is a multidisciplinary journal that specializes in the intersection between biology and materials science, chemistry, physics, engineering, and medicine. It covers various aspects such as the design and assembly of new structures, their interaction with biological systems, functionalization, bioimaging, therapies, and diagnostics in healthcare. The journal aims to showcase the most significant advancements and discoveries in this field. As part of the Materials Today family, Materials Today Bio provides rigorous peer review, quick decision-making, and high visibility for authors. It is indexed in Scopus, PubMed Central, Emerging Sources, Citation Index (ESCI), and Directory of Open Access Journals (DOAJ).
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