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Decellularized matrices for cardiovascular tissue engineering

机译:用于心血管组织工程的脱细胞基质

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摘要

Cardiovascular disease (CVD) is one of the leading causes of death in the Western world. The replacement of damaged vessels and valves has been practiced since the 1950’s. Synthetic grafts, usually made of bio-inert materials, are long-lasting and mechanically relevant, but fail when it comes to “biointegration”. Decellularized matrices, instead, can be considered biological grafts capable of stimulating in vivo migration and proliferation of endothelial cells (ECs), recruitment and differentiation of mural cells, finally, culminating in the formation of a biointegrated tissue. Decellularization protocols employ osmotic shock, ionic and non-ionic detergents, proteolitic digestions and DNase/RNase treatments; most of them effectively eliminate the cellular component, but show limitations in preserving the native structure of the extracellular matrix (ECM). In this review, we examine the current state of the art relative to decellularization techniques and biological performance of decellularized heart, valves and big vessels. Furthermore, we focus on the relevance of ECM components, native and resulting from decellularization, in mediating in vivo host response and determining repair and regeneration, as opposed to graft corruption.
机译:心血管疾病(CVD)是西方世界主要的死亡原因之一。自1950年代以来就开始更换损坏的容器和阀门。通常由生物惰性材料制成的人造移植物具有持久性并且在机械上具有相关性,但在“生物整合”方面却失败了。相反,可以认为脱细胞基质可以刺激内皮细胞(EC)的体内迁移和增殖,壁细胞的募集和分化,最终达到生物整合组织的形成的生物移植物。脱细胞方案采用渗透压,离子和非离子去污剂,蛋白水解酶和DNase / RNase处理。它们中的大多数有效地消除了细胞成分,但在保留细胞外基质(ECM)的天然结构方面显示出局限性。在这篇综述中,我们研究了与脱细胞技术以及脱细胞心脏,瓣膜和大血管的生物学性能相关的当前技术水平。此外,我们专注于天然和脱细胞产生的ECM成分在介导体内宿主反应以及确定修复和再生方面的相关性,而不是与移植物腐败相关。

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