DCECM/DBM-Radmscs复合支架作为高生物相容性角膜移植人工角膜裙

Shu-yan Cheng, Yue Li, Yifei Huang, S. Zhang, Zhao Li, H. Zhang, Liqiang Wang
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摘要

理想的人造角膜支架应具有良好的力学性能、较高的生物相容性、适当的耐腐蚀和耐磨性。由于材料的限制,角膜假体与角膜之间的韧性差异,经常导致角膜假体材料外露,从而导致严重的并发症。软骨具有与角膜相似的生物学特性,没有血管,具有一定的柔韧性。虽然使用耳软骨或肋软骨加固角膜假体已被证明是非常成功的,但不可能单独设计和理想化。迫切需要设计一种生物合成的软骨替代材料来应对这一困境。我们制备脱细胞软骨细胞外基质(DCECM)和脱细胞骨基质(DBM)并结合,加入兔脂肪源性间充质干细胞(rADMSCs)构建生物合成角膜假体裙。我们评估了DCECM/DBM-rADMSCs复合支架的力学性能、细胞结合效率、安全性和细胞毒性、生物相容性以及成软骨或成骨能力。实验结果表明,DCECM/DBM支架具有适当的弹性、韧性,对细胞安全。我们观察到DCECM/DBM-rADMSCs复合支架在移植12个月后能够完全融入受体角膜,无炎症和排斥反应。特别是,在支架内部甚至周围可以发现软骨和骨形成。因此,DCECM/DBM-rADMSCs复合支架可能是一种潜在的生物合成支架,用于角膜假体或固定支撑支架,以加强治疗终末期角膜失明的角膜假体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DCECM/DBM-Radmscs Composite Scaffold Acts as a Biosynthetic Keratoprosthesis Skirt with High Biocompatability for Corneal Transplantation
An ideal keratoprosthesis scaffold should have good mechanical property, high biocompatibility, suitable corrosion and wear resistance. Due to limitation of materials, the difference of tenacity between the keratoprosthesis and the cornea often causes the exposure of keratoprosthesis materials, which results in serious complications. The cartilage has the similar biological characteristics to the cornea, no blood vessels and has certain flexibility. Although using the auricular cartilage or rib cartilage to reinforce the keratoprosthesis has been proven greatly successful, it is not possible to be individually designed and idealized. It is urgent to design a biosynthetic material for cartilage replacement to deal with predicament. We prepared and combined the decellularized cartilage extracellular matrix (DCECM) and the decellularized bone matrix (DBM), added the rabbit adipose-derived mesenchymal stem cells (rADMSCs) to construct a biosynthetic keratoprosthesis skirt. We asssessed the mechanical property, cell binding efficiency, safety and cytotoxicity, biocompatability and chondrogenic or osteogenic capacity of the DCECM/DBM-rADMSCs composite scaffold. Tests revealed the DCECM/DBM scaffold has proper elasticity, tenacity, and, is safe to cells. It’s observed that the DCECM/DBM-rADMSCs composite scaffold integrated into the recipient cornea without inflammation and rejection, while transplanted in the recipient cornea for 12 months. In particular, chondrogenesis and osteogenesis are found inside and even around the scaffold. Hence, the DCECM/DBM-rADMSCs composite scaffold coule be a potential biosynthetic skirt for keratoprosthesis or a fixed supportive scaffold to reinforce the keratoprosthesis in the treatment of end-stage corneal blindness.
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