In Vitro Synthesis of a Microvascular Network

微血管网络的体外合成

• 批准号: 6726381
• 负责人: JOE Y TIEN
• 金额: $ 24.23万
• 依托单位: BOSTON UNIVERSITY (CHARLES RIVER CAMPUS)
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-09-30 至 2005-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6726381
• 关键词: anatomy; angiogenesis; artificial skin; bioengineering /biomedical engineering; biotechnology; blood vessels; capillary bed; cell component structure /function; confocal scanning microscopy; cytokine; fibroblasts; human tissue; immunofluorescence technique; inflammation; microcirculation; molecular film; oxidative stress; shear stress; skin circulation; tissue engineering; vascular endothelium; vascular smooth muscle; video microscopy

DESCRIPTION (provided by applicant): This two-year proposal describes the development of processes, based on microlithography, to synthesize a human dermal microvascular network in vitro. The methods developed in this work will support the following long-term goals: 1) modeling of human inflammatory responses in vitro for high-throughput screening of agents that can reverse an induced response, and 2) engineering of full-thickness skin grafts with an integrated vasculature. By allowing the synthesis of tissue with a controlled microscale architecture, these lithographic methods will complement current strategies in tissue engineering that rely on cellular self-organization induced by growth factors. The proposed schemes will arrange primary microvascular cells into a three-dimensional network of open tubes initially, and then continuously perfuse the construct to allow its maturation into a functional microcirculation. We will determine the ranges of network shear stress, luminal pressure, and oxidative stress that enable the as-synthesized construct to develop a histological organization characteristic of a human dermal microvascular bed. Moreover, we will vary perfusion conditions to tune the reactivity of the in vitro network to inflammatory cytokines, and to enhance the extravasation of neutrophils in a stimulated network. This work will further determine the thickness of tissue that can be sustained metabolically by an engineered microvascular construct comprised of two interconnected plexuses.

描述（由申请人提供）：这份为期两年的提案描述了基于显微光刻术在体外合成人类真皮微血管网络的过程的开发。在这项工作中开发的方法将支持以下长期目标：1）体外人类炎症反应的建模，用于高通量筛选可以逆转诱导反应的试剂，以及2）具有集成脉管系统的全层皮肤移植物的工程设计。通过允许合成具有受控微尺度结构的组织，这些光刻方法将补充依赖于生长因子诱导的细胞自组织的组织工程中的当前策略。所提出的方案最初将原代微血管细胞排列成开放管的三维网络，然后持续灌注该构造以使其成熟为功能性微循环。我们将确定网络剪切应力，管腔压力和氧化应激的范围，使合成的构建体能够发展出人类真皮微血管床的组织学组织特征。此外，我们将改变灌注条件来调节体外网络对炎性细胞因子的反应性，并增强受刺激网络中中性粒细胞的外渗。这项工作将进一步确定组织的厚度，可以通过由两个相互连接的丛组成的工程微血管结构来维持代谢。