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Integration of C-type natriuretic peptide gene-modified bone marrow mesenchymal stem cells with chitosan/silk fibroin scaffolds as a promising strategy for articular cartilage regeneration

机译:C型Natriuretic肽基因改性骨髓间充质干细胞与壳聚糖/丝素蛋白支架的整合作为关节软骨再生的有希望的策略

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摘要

The treatment of articular cartilage defects has become a major clinical concern. Currently, additional efforts are necessary to develop effective methods to cure this disease. In this work, we combined gene therapy with tissue engineering methods to test their effect on cartilage repair. In in vitro experiments, we obtained C-type natriuretic peptide (CNP) gene-modified bone marrow-derived mesenchymal stem cells (BMSCs) by transfection with recombinant adenovirus containing the CNP gene and revealed that CNP gene-modified BMSCs had good chondrogenic differentiation ability. By the freeze-drying method, we successfully synthesized a chitosan/silk fibroin (CS/SF) porous scaffold, which had a suitable aperture size for chondrogenesis. Then, we loaded CNP gene-modified BMSCs onto CS/SF scaffolds and tested their effect on repairing full-thickness cartilage defects in rat joints. The gross morphology and histology examination results showed that the composite of the CNP gene-modified BMSCs and CS/SF scaffolds had better repair effects than those of the other three groups at each time point. Additionally, compared to the group with BMSCs and scaffolds, we found that there was more cartilage matrix in the CNP gene-modified BMSCs and CS/SF scaffolds group. Data obtained in the present study suggest that the composite of CNP gene-modified BMSCs and CS/SF scaffolds represent promising strategies for repairing focal cartilage lesions.
机译:关节软骨缺陷的治疗已成为一个主要的临床关注。目前,需要额外的努力来制定有效的方法来治愈这种疾病。在这项工作中,我们将基因治疗与组织工程方法合并以测试它们对软骨修复的影响。在体外实验中,我们通过用含有CNP基因的重组腺病毒转染并显示CNP基因改性BMSCs具有良好的软骨内分化能力,得到C型Natrietic肽(CNP)基因改性的骨髓衍生的间充质干细胞(BMSC) 。通过冷冻干燥方法,我们成功地合成了一种壳聚糖/丝素蛋白(CS / SF)多孔支架,其具有适当的软骨发生孔径。然后,我们将CNP基因改性的BMSC加载到CS / SF支架上,并测试了它们对修复大鼠接头中的全厚软骨缺陷的影响。总体形态和组织学检查结果表明,CNP基因改性BMSCs和CS / SF支架的复合材料比在每个时间点的其他三组的修复效果更好。另外,与具有BMSCs和支架的组相比,我们发现CNP基因改性BMSC和CS / SF支架基团中有更多的软骨基质。本研究中获得的数据表明CNP基因改性BMSC和CS / SF支架的复合材料代表了修复局灶性软骨病变的有希望的策略。

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