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Preparation of calcium silicate/decellularized porcine myocardial matrix crosslinked by procyanidins for cardiac tissue engineering

机译:硅酸钙/脱细胞的猪心肌基质的制备交联由胰岛组织工程

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摘要

Decellularized myocardial extracellular matrix (ECM) patches have promising potential for myocardial repair, due to the well-preserved compositional cues, good biocompatibility and non-immunogenicity. However, the lack of vascularization and their low mechanical properties, chemical instability caused by decellularization process limit their application in cardiac tissue engineering. Therefore, we used calcium silicate (CS) extracts interpenetration method to prepare CS-loaded bioactive scaffold, since CS bioceramic was reported to have stimulative effect on angiogenesis. Meanwhile, procyanidins (PC), a natural plant polyphenol, was utilized to crosslink the decellularized myocardial ECMs, aiming at enhancing the mechanical properties and resistance to enzymatic proteolysis. The results showed that PC-crosslinked pcECMs displayed great crosslinking stability and efficiency, improved tensile strength and chemical stability as compared with non-crosslinked group, and the enhancement was depended on the concentration of PC. The CS-loaded ECMs showed stable Ca and Si ions release during 7 days and the ion concentration was adjusted in the range with angiogenic potential by controlling the original concentration of CS extracts. Cytotoxicity assay showed that the CS-loaded pcECMs crosslinked by PC were cytocompatible for supporting the adhesion and proliferation of H9c2 cardiomyoblasts, endothelial cells and fibroblasts. Moreover, the CS incorporating could enhance the proliferation rate and angiogenic gene expression of endothelial cells effectively. These findings verified the feasibility of PC crosslinking and CS incorporation as a novel approach to prepare bioactive complex decellularized myocardial scaffold, which can be applied to cardiac tissue engineering for myocardial repair.
机译:心肌修复,由于保存完好的成分线索,良好的生物相容性,无免疫原性脱细胞的心肌细胞外基质(ECM)补丁看好的潜力。但是,由于缺乏血管和其低的机械性能,化学不稳定性造成的细胞化过程中限制其在心脏组织工程中的应用。因此,我们使用硅酸钙(CS)的萃取液穿插方法制备CS-装载生物活性支架,由于生物陶瓷CS被报道具有对血管生成促进作用。同时,原花青素(PC),天然植物多酚,被用来交联的脱细胞的心肌ECM中,针对增强的机械性能和抗酶促蛋白水解。结果表明,PC-交联pcECMs表现出极大的交联稳定性和效率,改进的拉伸强度和化学稳定性,非交联的组相比,和增强了依赖于PC的浓度。的CS-加载的ECM在7天期间表现出稳定的Ca和Si离子释放和离子浓度与通过控制CS提取物的初始浓度的血管生成潜力的范围内调整。细胞毒性分析表明,由PC的交联的CS-加载pcECMs是细胞相容性,用于支撑的H9c2心肌细胞,内皮细胞和成纤维细胞的粘附和增殖。此外,CS能够掺入有效增强内皮细胞的增殖速率和血管生成基因的表达。这些发现证实PC交联和CS掺入的可行性作为一种新的方法,以制备生物活性复合物脱细胞的心肌的支架,其可被施加到心脏组织工程用于心肌修复。

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  • 来源
    《RSC Advances》 |2016年第41期|共11页
  • 作者单位

    Chinese Acad Sci Shanghai Inst Ceram State Key Lab High Performance Ceram &

    Superfine 1295 Dingxi Rd Shanghai 200050 Peoples R China;

    Chinese Acad Sci Shanghai Inst Ceram State Key Lab High Performance Ceram &

    Superfine 1295 Dingxi Rd Shanghai 200050 Peoples R China;

    Chinese Acad Sci Shanghai Inst Ceram State Key Lab High Performance Ceram &

    Superfine 1295 Dingxi Rd Shanghai 200050 Peoples R China;

    Chinese Acad Sci Shanghai Inst Ceram State Key Lab High Performance Ceram &

    Superfine 1295 Dingxi Rd Shanghai 200050 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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