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首页> 外文期刊>BioMed research international >Immobilized Lentivirus Vector on Chondroitin Sulfate-Hyaluronate Acid-Silk Fibroin Hybrid Scaffold for Tissue-Engineered Ligament-Bone Junction
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Immobilized Lentivirus Vector on Chondroitin Sulfate-Hyaluronate Acid-Silk Fibroin Hybrid Scaffold for Tissue-Engineered Ligament-Bone Junction

机译:硫酸软骨素-透明质酸-丝素蛋白混合支架上固定的慢病毒载体用于组织工程韧带-骨连接的研究

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摘要

The lack of a fibrocartilage layer between graft and bone remains the leading cause of graft failure after anterior cruciate ligament (ACL) reconstruction. The objective of this study was to develop a gene-modified silk cable-reinforced chondroitin sulfate-hyaluronate acid-silk fibroin (CHS) hybrid scaffold for reconstructing the fibrocartilage layer. The scaffold was fabricated by lyophilizing the CHS mixture with braided silk cables. The scanning electronic microscopy (SEM) showed that microporous CHS sponges were formed around silk cables. Each end of scaffold was modified with lentiviral-mediated transforming growth factor-beta3 (TGF-beta3) gene. The cells on scaffold were transfected by bonded lentivirus. In vitro culture demonstrated that mesenchymal stem cells (MSCs) on scaffolds proliferated vigorously and produced abundant collagen. The transcription levels of cartilage-specific genes also increased with culture time. After 2 weeks, the MSCs were distributed uniformly throughout scaffold. Deposited collagen was also found to increase. The chondral differentiation of MSCs was verified by expressions of collagen II and TGF-beta3 genes in mRNA and protein level. Histology also confirmed the production of cartilage extracellular matrix (ECM) components. The results demonstrated that gene-modified silk cable-reinforced CHS scaffold was capable of supporting cell proliferation and differentiation to reconstruct the cartilage layer of interface.
机译:在前交叉韧带(ACL)重建后,移植物和骨之间缺乏纤维软骨层仍然是移植失败的主要原因。这项研究的目的是开发基因改造的丝线增强硫酸软骨素-透明质酸-丝素蛋白(CHS)混合支架,以重建纤维软骨层。通过将CHS混合物与编织的丝缆冻干来制造支架。扫描电子显微镜(SEM)显示,在丝缆周围形成了微孔CHS海绵。支架的每个末端都用慢病毒介导的转化生长因子-beta3(TGF-beta3)基因进行了修饰。用结合的慢病毒转染支架上的细胞。体外培养表明,支架上的间充质干细胞(MSC)大量增殖并产生丰富的胶原蛋白。软骨特异性基因的转录水平也随着培养时间的增加而增加。 2周后,将MSC均匀地分布在整个支架中。还发现沉积的胶原蛋白增加。 MSCs的软骨分化通过mRNA和蛋白水平中II型胶原和TGF-β3基因的表达得以证实。组织学还证实了软骨细胞外基质(ECM)成分的产生。结果表明,基因修饰的丝线增强的CHS支架能够支持细胞增殖和分化,以重建界面的软骨层。

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