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Osteochondral scaffold combined with aligned nanofibrous scaffolds for cartilage regeneration

机译:骨软骨支架与对齐的纳米纤维支架相结合用于软骨再生

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Osteochondral defect repair poses a significant challenge in its reconstruction as the damage is presented in both articular cartilage and the underlying subchondral bone. Tissue engineering approaches have utilized various scaffolds in combination of stem cells and growth factors to regenerate the defect. Still a significant challenge remains in creating a scaffold structure that supports the proliferation and differentiation of bone marrow stromal cells (BMSCs) into chondrocytes and osteoblasts while providing the appropriate mechanical stability. The present manuscript reports the fabrication and characterization of a biphasic scaffold system derived from biodegradable polymers such as poly(lactic acid-glycolic acid) (PLGA) as a hard shell and polycaprolactone (PCL) a soft component. Collectively this biphasic scaffold was able to withstand physiological loads up to 10 000 cycles in a cyclic compressive test. The scaffold surface was decorated with PCL aligned nanofibers contacting chondroitin sulfate and hyaluronic acid and nanofibers were cross-linked via carbodiimide linkages to retain these bioactive molecules over the culture period. The present study aims to show the potential of these bioactive scaffolds for the repair of osteochondral defects. Scaffolds were characterized by Fourier transform infra-red spectroscopy, optical microscopy and cyclic compressive testing. Primary rat bone marrow stem cells were seeded onto scaffolds and cell proliferation and differentiation was evaluated using RTPCR and immunohistochemistry. RT-PCR indicated that the scaffold was able to stimulate the different regions of osteochondral tissue: collagen type II and aggrecan expression in the cartilage region and BMP-2 in the bone region. Similarly protein secretion with induced alignment was confirmed with immunofluorescence imaging. This novel hybrid scaffold shows promising results in the regeneration of cartilage tissue as well as the underlying subchondral bone.
机译:骨软骨缺损修复在其重建中提出了重大挑战,因为在关节软骨和下面的软骨下骨中都存在损伤。组织工程方法已利用各种支架结合干细胞和生长因子来再生缺损。在创建支持骨髓基质细胞(BMSC)增殖和分化为软骨细胞和成骨细胞同时提供适当机械稳定性的支架结构方面,仍然存在重大挑战。本手稿报告了一种双相支架系统的制造和表征,该系统由可生物降解的聚合物(如聚乳酸-乙醇酸(PLGA)作为硬壳,聚己内酯(PCL)作为软组分)衍生而来。总体而言,这种双相支架在循环压缩试验中能够承受高达10,000个循环的生理负荷。用与硫酸软骨素和透明质酸接触的PCL对齐纳米纤维装饰支架表面,并通过碳二亚胺键交联纳米纤维,以在培养期间保留这些生物活性分子。本研究旨在显示这些生物活性支架修复骨软骨缺损的潜力。通过傅立叶变换红外光谱,光学显微镜和循环压缩测试对支架进行表征。将大鼠原代骨髓干细胞接种到支架上,并使用RTPCR和免疫组织化学评估细胞的增殖和分化。 RT-PCR表明该支架能够刺激骨软骨组织的不同区域:软骨区域中II型胶原蛋白和聚集蛋白聚糖的表达以及骨骼区域中BMP-2的表达。类似地,通过免疫荧光成像证实了具有诱导的比对的蛋白质分泌。这种新型的混合支架在软骨组织以及软骨下骨的再生中显示出令人鼓舞的结果。

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