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Repair of rabbit osteochondral defects by an acellular technique with an ultrapurified alginate gel containing stromal cell-derived factor-1

机译:含有基质细胞衍生因子1的超纯化藻酸盐凝胶通过脱细胞技术修复兔软骨软骨缺损

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The objective of this study was to determine whether the local administration of stromal cell-derived factor-1 (SDF-1) using ultrapurified alginate gel (UPAL gel) could improve reparative tissues of osteochondral defects compared with those without treatment. For the investigation, a full-thickness osteochondral defect 4.5mm in diameter and 3mm in depth was created in the patella groove of the distal femur in rabbits. Local expression of SDF-1 protein was temporarily upregulated at 1 week after creating the osteochondral defect. The local administration of SDF-1 enhanced the migration of host cells, mainly bone marrow stromal cells (BMSCs), to the site of the osteochondral defect. In vitro cell migration assay supported this result. In the SDF-1 (UPAL gel containing SDF-1) treatment group, the histological scores and the compressive modulus of reparative tissues were significantly improved compared with the no-treatment and vehicle (UPAL gel without SDF-1) groups. On the other hand, SDF-1 did not influence the cellular proliferation and chondrogenesis of BMSCs. Based on the results obtained here, we speculate that SDF-1 enhances the reparative process of osteochondral injuries not through direct effects on the behavior of host cells, but through increased migration of host cells to the injured site. UPAL gel, as a vehicle material, may play an important role in chondrogenesis of recruited cells, mainly BMSCs. The cell-free approach with local administration of SDF-1 may be an effective strategy for developing a minimally invasive technique for cartilage tissue regeneration.
机译:这项研究的目的是确定与不治疗相比,使用超纯化藻酸盐凝胶(UPAL凝胶)局部施用基质细胞衍生因子-1(SDF-1)是否可以改善骨软骨缺损的修复组织。为了进行研究,在兔股骨远端的骨沟中形成了直径4.5mm,深度3mm的全厚度骨软骨缺损。 SDF-1蛋白的局部表达在产生骨软骨缺损后1周被暂时上调。 SDF-1的局部给药增强了宿主细胞(主要是骨髓基质细胞(BMSC))向骨软骨缺损部位的迁移。体外细胞迁移测定支持该结果。在SDF-1(含SDF-1的UPAL凝胶)治疗组中,修复组织的组织学评分和压缩模量与未治疗和赋形剂(无SDF-1的UPAL凝胶)组相比有显着改善。另一方面,SDF-1不影响BMSCs的细胞增殖和软骨形成。基于此处获得的结果,我们推测SDF-1不是通过直接影响宿主细胞的行为,而是通过增加宿主细胞向受伤部位的迁移来增强骨软骨损伤的修复过程。 UPAL凝胶作为一种载体材料,可能在募集细胞(主要是BMSC)的软骨形成中发挥重要作用。局部施用SDF-1的无细胞方法可能是开发用于软骨组织再生的微创技术的有效策略。

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