Department of Sports Medicine, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, 600 Yishan Road, Shanghai 200233, China.
ACS Biomater Sci Eng. 2020 Oct 12;6(10):5700-5710. doi: 10.1021/acsbiomaterials.0c00269. Epub 2020 Sep 24.
Anterior cruciate ligament (ACL) reconstruction with allografts is limited by high immunogenicity, poor cellularization, and delayed tendon-bone healing. Decellularized tendons (DAs) have been used as bioscaffolds to reconstruct ligaments with variable success. In the study, four kinds of decellularized allogeneic hamstring tendons were prepared and their microstructure and cytocompatibility were examined in vitro. The results showed that decellularized allografts neutralized by 5% calcium bicarbonate had typical reticular and porous microstructures with optical cytocompatibility. Tissue-engineering decellularized allografts (TEDAs) were prepared with the selected decellularized allografts and tendon stem/progenitor cells and used for ACL reconstruction in a rabbit model. Histological staining showed that the TEDAs promoted cellular infiltration and new vessel formation significantly and improved tendon-bone healing moderately compared to decellularized allografts. Better macroscopic scores and biomechanical results were observed in TEDA groups, but there were no significant differences between DA and TEDA groups at months 1, 2, and 3 postoperatively. Immunohistochemical data showed that the tissue-engineering decellularized allografts enhanced the expression of collagen I at each timepoint and collagen III at months 1 and 2. ELISA analysis showed that the tissue-engineering decellularized allografts reduced the secretion of IgE and IL-1β within 1 month and promoted the secretion of IL-2, IL-4, IL-10, and IL-17 after 1 month. The results showed that tissue-engineering decellularized allografts strengthened intra-articular graft remodeling significantly and provided moderate improvements in tendon-bone healing by creating more suitable immune responses than decellularized allografts. The study revealed that tissue-engineering decellularized allografts as a promising option for ACL reconstruction could achieve more favorable outcomes.
前交叉韧带(ACL)重建用同种异体移植物受到高免疫原性、细胞化不良和延迟的腱骨愈合的限制。脱细胞肌腱(DAs)已被用作生物支架,以不同程度成功重建韧带。在研究中,制备了四种脱细胞同种异体肌腱,并在体外检查了它们的微观结构和细胞相容性。结果表明,用 5%碳酸氢钙中和的脱细胞同种异体移植物具有典型的网状和多孔微观结构,具有光学细胞相容性。使用选定的脱细胞同种异体移植物和肌腱干/祖细胞制备组织工程脱细胞同种异体移植物(TEDAs),并将其用于兔 ACL 重建模型。组织学染色显示,与脱细胞同种异体移植物相比,TEDAs 显著促进细胞浸润和新血管形成,并适度改善腱骨愈合。在 TEDA 组中观察到更好的宏观评分和生物力学结果,但在术后 1、2 和 3 个月时,DA 和 TEDA 组之间没有显著差异。免疫组织化学数据显示,组织工程脱细胞同种异体移植物在每个时间点增强了胶原 I 的表达,在 1 和 2 个月时增强了胶原 III 的表达。ELISA 分析显示,组织工程脱细胞同种异体移植物在 1 个月内减少了 IgE 和 IL-1β 的分泌,并在 1 个月后促进了 IL-2、IL-4、IL-10 和 IL-17 的分泌。结果表明,组织工程脱细胞同种异体移植物通过产生更合适的免疫反应,显著增强了关节内移植物重塑,并适度改善了腱骨愈合。该研究表明,组织工程脱细胞同种异体移植物作为 ACL 重建的一种有前途的选择,可以通过产生更合适的免疫反应来实现更有利的结果。