Institute of Combined Injury, State Key Laboratory of Trauma, Burns and Combined Injury, Chongqing Engineering Research Center for Nanomedicine, College of Preventive Medicine, Third Military Medical University, Chongqing, China; Key Laboratory for Nano-Bio Interface Research, Suzhou Key Laboratory for Nanotheranostics, Division of Nanobiomedicine, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou, China.
Key Laboratory for Nano-Bio Interface Research, Suzhou Key Laboratory for Nanotheranostics, Division of Nanobiomedicine, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou, China.
Biomaterials. 2018 Apr;162:22-33. doi: 10.1016/j.biomaterials.2018.02.008. Epub 2018 Feb 4.
It had been demonstrated that stromal cell-derived factor-1α (SDF-1α) could promote in situ tendon regeneration by recruiting endogenous cells. However, native SDF-1α diffuses too fast in vivo, reducing its local concentration and efficacy. In this study, we prepared a recombinant SDF-1α containing a collagen-binding domain (CBD-SDF-1α) and developed a functional collagen scaffold by tethering CBD-SDF-1α on the collagen scaffold for in situ tendon regeneration. CBD-SDF-1α could induce the migration of mesenchymal stem cells, dermal fibroblasts and Achilles tendon fibroblasts in vitro, and achieve controlled release from the collagen scaffold. In a rat Achilles tendon defect model, the functional scaffold could increase the recruitment of CXCR4 positive fibroblast-like cells and the deposition of Tenascin-C at 7 days after implantation. After 4 and 12 weeks, the functional collagen scaffold could promote the expression of type I collagen, increase the diameters of collagen fibrils and improve the mechanical properties of regenerated tendons. Hence, the functional scaffold increased the efficacy of tendon regeneration by controlling release of SDF-1α, enhancing the recruitment of fibroblast-like cells and providing instructive microenvironment and mechanical support for tendon regeneration. Therefore, CBD-SDF-1α-modified collagen scaffold could serve as a practical application for tendon regeneration.
已有研究表明,基质细胞衍生因子-1α(SDF-1α)可通过募集内源性细胞来促进原位肌腱再生。然而,天然 SDF-1α 在体内扩散过快,导致其局部浓度和效果降低。本研究制备了一种含有胶原结合域(CBD-SDF-1α)的重组 SDF-1α,并通过将 CBD-SDF-1α 固定在胶原支架上来开发功能性胶原支架,以实现原位肌腱再生。CBD-SDF-1α 可诱导间充质干细胞、真皮成纤维细胞和跟腱成纤维细胞在体外迁移,并从胶原支架中实现受控释放。在大鼠跟腱缺损模型中,功能性支架可增加 CXCR4 阳性成纤维样细胞的募集和腱糖蛋白-C 的沉积,在植入后 7 天。4 周和 12 周后,功能性胶原支架可促进 I 型胶原的表达,增加胶原纤维直径,并改善再生肌腱的机械性能。因此,通过控制 SDF-1α 的释放、增强成纤维样细胞的募集以及为肌腱再生提供指导微环境和机械支持,功能性支架提高了肌腱再生的效果。因此,CBD-SDF-1α 修饰的胶原支架可作为肌腱再生的一种实用应用。