Suppr超能文献

用于人工组织和器官生成的血管化支架工程。

Engineering of a vascularized scaffold for artificial tissue and organ generation.

作者信息

Mertsching Heike, Walles Thorsten, Hofmann Michael, Schanz Johanna, Knapp Wolfram H

机构信息

Fraunhofer Institute for Interfacial Engineering and Biotechnology, Nobelstrasse 12, 70569 Stuttgart, Germany.

出版信息

Biomaterials. 2005 Nov;26(33):6610-7. doi: 10.1016/j.biomaterials.2005.04.048.

Abstract

Tissue engineering is an emerging field in regenerative medicine to overcome the problem of end-stage organ failure. However, complex tissues and organs need a vascular supply to guaranty graft survival and render bioartificial organ function. Here we developed methods to decellularize porcine small bowl segments and repopulate the remaining venous and arterial tubular structures within these matrices with allogeneic porcine endothelial progenitor cells. Cellular adherence and vitality was characterized by quantitative 2-[18F]-fluoro-2'-desoxy-glucose (FDG) positron emission tomography (PET) and subsequent immunohistological work up. The generated matrices showed insulin-dependent FDG uptake predominantly in the region of the former vascular structures. Stain for vitality and the specific endothelial markers CD31, VE-Cadherin and Flk-1 matched this functional finding. Providing evidence for vitality up to 3 weeks post reconstitution and typical endothelial differentiation, these results indicate that our generated matrix allows the generation of complex bioartificial tissues and organs for experimental and future clinical application.

摘要

组织工程是再生医学中一个新兴的领域,旨在克服终末期器官衰竭的问题。然而,复杂的组织和器官需要血管供应来保证移植存活并实现生物人工器官功能。在此,我们开发了使猪小肠段去细胞化的方法,并用同种异体猪内皮祖细胞重新填充这些基质内剩余的静脉和动脉管状结构。通过定量2-[18F]-氟-2'-脱氧葡萄糖(FDG)正电子发射断层扫描(PET)及随后的免疫组织学检查来表征细胞黏附和活力。生成的基质显示胰岛素依赖性FDG摄取主要在前血管结构区域。活力染色以及特异性内皮标志物CD31、血管内皮钙黏蛋白(VE-Cadherin)和Flk-1与这一功能发现相符。这些结果为重建后长达3周的活力以及典型的内皮分化提供了证据,表明我们生成的基质能够生成用于实验和未来临床应用的复杂生物人工组织和器官。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验