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首页> 外文期刊>Tissue engineering >Transplantation of allogeneic chondrocytes cultured in fibroin sponge and stirring chamber to promote cartilage regeneration.
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Transplantation of allogeneic chondrocytes cultured in fibroin sponge and stirring chamber to promote cartilage regeneration.

机译:在纤维蛋白海绵和搅拌室中培养的同种异体软骨细胞的移植,以促进软骨再生。

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Cartilage regeneration using a fibroin sponge and a stirring chamber was investigated to improve the potential of articular cartilage tissue engineering. Chondrocytes seeded on the fibroin-sponge scaffolds were cultured in the stirring chamber (a bioreactor facilitating mechanical stimulation) for up to 3 weeks. Changes in DNA content, glycosaminoglycan (GAG) amount, integrin subunits alpha5 and beta1 fluorescence intensity, and morphologic appearance, were studied to evaluate tissue maturity. Seeded scaffolds subjected to the stirring chamber demonstrated significant increases in both DNA content (38.9%) and GAG content (54.3%) at day 21 compared to the control group. In addition, the stirring chamber system facilitated a maturation of cartilage tissue showed by histologic examination, after a staining of proteoglycan and type II collagen. Clinical feasibility of the fibroin and stirring chamber system was evaluated using rabbit models with cartilage defect. Large defects on rabbit knee joints were repaired with regenerated cartilage, which resembles hyaline cartilage at 12 weeks after operation. These studies demonstrated the potential of such mechanically stimulated scaffold/cell constructs to support chondrogenesis in vivo.
机译:使用纤维蛋白海绵和搅拌腔进行软骨再生的研究,以提高关节软骨组织工程的潜力。在搅拌室(促进机械刺激的生物反应器)中培养接种在纤维蛋白海绵支架上的软骨细胞长达3周。研究了DNA含量,糖胺聚糖(GAG)量,整联蛋白亚基alpha5和beta1荧光强度以及形态外观的变化,以评估组织的成熟度。与对照组相比,经过搅拌的种子支架在第21天的DNA含量(38.9%)和GAG含量(54.3%)均显着增加。另外,在对蛋白聚糖和II型胶原染色之后,搅拌室系统促进了通过组织学检查显示的软骨组织的成熟。使用具有软骨缺损的兔子模型评估了纤维蛋白和搅拌室系统的临床可行性。兔膝关节的大缺损用再生软骨修复,类似于术后12周的透明软骨。这些研究证明了这种机械刺激的支架/细胞构建体在体内支持软骨形成的潜力。

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