Suppr超能文献

构建微循环。

Engineering the microcirculation.

作者信息

Lokmic Zerina, Mitchell Geraldine M

机构信息

Bernard O'Brien Institute of Microsurgery, Melbourne, Victoria, Australia.

出版信息

Tissue Eng Part B Rev. 2008 Mar;14(1):87-103. doi: 10.1089/teb.2007.0299.

Abstract

The ultimate survival of tissue-engineered constructs in vivo depends on the provision of an adequate blood supply to the engineered tissue and the capacity of the engineered microcirculation to connect with the existing recipient circulation. Techniques for the vascularization of tissue-engineered constructs can be broadly grouped into in vitro and in vivo approaches that rely on the presence of a pro-angiogenic microenvironment. Significant advances have been made in resolving the problem of microcirculatory network formation for large 3-dimensional constructs; however, issues concerning construct-host vessel connection, expansion of vascular volume accompanying growing tissue, and prevention of premature or excessive vascular regression remain to be resolved. This review provides an overview of current approaches to creating microcirculatory networks with respect to the cells involved, growth factors, growth factor delivery systems, and scaffold properties required to engineer a permanent microcirculatory network for tissue-engineered constructs. In addition, the review examines concerns related to vascular remodeling and regression reported in some tissue-engineering models.

摘要

组织工程构建体在体内的最终存活取决于为工程组织提供充足的血液供应,以及工程化微循环与现有受体循环建立连接的能力。组织工程构建体的血管化技术可大致分为体外和体内方法,这些方法依赖于促血管生成微环境的存在。在解决大型三维构建体的微循环网络形成问题方面已取得重大进展;然而,关于构建体与宿主血管连接、伴随组织生长的血管体积扩张以及预防过早或过度的血管消退等问题仍有待解决。本综述概述了当前创建微循环网络的方法,涉及参与的细胞、生长因子、生长因子递送系统以及为组织工程构建体构建永久性微循环网络所需的支架特性。此外,该综述还探讨了一些组织工程模型中报道的与血管重塑和消退相关的问题。

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