Zhen Zhang, Xu Hu, Min Jin, Yulei Mu, Huiqun Zhou, Cheng Ma, Liang Ma, Bangheng Liu, Hang Yao, Ye Huang, Dong-An Wang
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引用次数: 0
摘要
长期以来,修复和再生关节软骨缺损(ACD)一直是医生和科学家面临的挑战。可注射材料的兴起为微创手术修复 ACD 提供了一种新策略。在这项研究中,我们成功开发了基于 II 型胶原蛋白的可注射材料,实现了 ACD 的透明软骨修复和再生。我们对注射材料后的再生软骨进行了分析。组织学染色显示 ACD 完全愈合,并达到了透明软骨表型。其生化和生物力学特性与邻近的原生软骨相似,对软骨下骨没有明显的不良影响。进一步的转录组分析发现,与缺损区邻近的原生软骨相比,用 II 型胶原注射材料修复的缺损区再生软骨显示出软骨相关通路的变化,以及 T 细胞受体信号通路和白细胞介素-17 信号通路的下调,这改变了 ACD 区的免疫微环境。总之,这些研究结果为治疗 ACD 提供了一种前景广阔的注射方法,为解决与实现透明软骨原位修复和再生相关的挑战提供了一种潜在的解决方案,同时最大限度地减少了对周围软骨的损伤。
Collagen Type II-Based Injectable Materials for In situ Repair and Regeneration of Articular Cartilage Defect.
Repairing and regenerating articular cartilage defects (ACDs) have long been challenging for physicians and scientists. The rise of injectable materials provides a novel strategy for minimally invasive surgery to repair ACDs. In this study, we successfully developed injectable materials based on collagen type II, achieving hyaline cartilage repair and regeneration of ACDs. Analysis was conducted on the regenerated cartilage after materials injection. The histology staining demonstrated complete healing of the ACDs with the attainment of a hyaline cartilage phenotype. The biochemical and biomechanical properties are similar to the adjacent native cartilage without noticeable adverse effects on the subchondral bone. Further transcriptome analysis found that compared with the Native cartilage adjacent to the defect area, the Regenerated cartilage in the defect area repaired with type II collagen-based injection materials showed changes in cartilage-related pathways, as well as down-regulation of T cell receptor signaling pathways and interleukin-17 signaling pathways, which changed the immune microenvironment of the ACD area. Overall, these findings offer a promising injectable approach to treating ACDs, providing a potential solution to the challenges associated with achieving hyaline cartilage in situ repair and regeneration while minimizing damage to the surrounding cartilage.