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首页> 外文期刊>Artificial cells, blood substitutes, and biotechnology >Decellularization of heart valve matrices: search for the ideal balance.
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Decellularization of heart valve matrices: search for the ideal balance.

机译:心脏瓣膜基质的脱细胞作用:寻求理想的平衡。

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摘要

Currently used decellularization procedures have negative effects on extracellular matrix (ECM) integrity. The objective of this study is to evaluate four decellularization methods and their effect on the collagen ultrastructure, mechanical behavior and antigenicity of porcine aortic valves.Aortic valves were placed in a trypsin, osmotic, trypsin-osmotic or detergent-osmotic solution. Leaflets were processed for histology and mechanical testing. Matrices were implanted subdermally in rats to evaluate immune reaction and calcification.Trypsin-osmotic methodology effected near-complete decellularization. Trypsin treatment resulted in cell removal only in the spongiosa layer. Osmotic and detergent-osmotic treatments did not remove any cells from the cusps. Mechanical strength was significantly inferior in the trypsin (p50,03) and trypsin-osmotic treated group (p50,04). Trypsin and trypsin-osmotic decellularized matrices evoked a strong CD31 inflammatory cell infiltration.Enzymatic-osmotic decellularization appears to be the only effective method to remove cellular components. However, the near cell free scaffolds still evokes a strong CD31 T-cell inflammatory reaction.
机译:当前使用的脱细胞程序对细胞外基质(ECM)完整性有负面影响。本研究的目的是评估四种脱细胞方法及其对猪主动脉瓣膜胶原超微结构,机械行为和抗原性的影响。对传单进行了组织学和机械测试。将基质皮下植入大鼠皮下以评估免疫反应和钙化。胰蛋白酶渗透法几乎完成了脱细胞作用。胰蛋白酶处理仅在海绵层中导致细胞去除。渗透和去污剂渗透处理没有从牙尖去除任何细胞。胰蛋白酶(p50,03)和胰蛋白酶渗透处理组(p50,04)的机械强度明显较差。胰蛋白酶和胰蛋白酶渗透脱细胞基质引起强烈的CD31炎症细胞浸润,酶渗透脱细胞似乎是去除细胞成分的唯一有效方法。但是,无细胞的支架仍会引起强烈的CD31 T细胞炎症反应。

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