用于心血管组织工程的脱细胞基质。

IF 1.5 Q4 CELL BIOLOGY American journal of stem cells Pub Date : 2014-03-13 eCollection Date: 2014-01-01
Francesco Moroni, Teodelinda Mirabella
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引用次数: 0

摘要

心血管疾病(CVD)是西方世界的主要死因之一。自 20 世纪 50 年代起,人们就开始对受损血管和瓣膜进行置换。合成移植物通常由生物惰性材料制成,具有持久性和机械相关性,但在 "生物整合 "方面却不尽如人意。而脱细胞基质可被视为生物移植物,能够刺激体内内皮细胞(EC)的迁移和增殖,壁细胞的招募和分化,最终形成生物整合组织。脱细胞方案采用了渗透冲击、离子和非离子洗涤剂、蛋白溶解和 DNase/RNase 处理等方法;其中大多数都能有效消除细胞成分,但在保留细胞外基质(ECM)的原生结构方面存在局限性。在这篇综述中,我们研究了脱细胞技术的现状以及脱细胞心脏、瓣膜和大血管的生物学性能。此外,我们还将重点关注原生和脱细胞后的 ECM 成分在介导体内宿主反应、决定修复和再生(而非移植物损坏)方面的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Decellularized matrices for cardiovascular tissue engineering.

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.

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