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Full Text urn:etd:azu_etd_2555_sip1_m
Title Development of In Vitro Three-Dimensional Microvascular Tissues
Author Carlos Chang
Affiliation University of Arizona
Advisor James B Hoying
Date 2008-3-06 00:00:00
Degree Ph.D.
Language English
Major Biomedical Engineering
Keywords tissue engineer microvessels; microvascular engineering; perfusion
Abstract Microvasculatures may become damaged by a variety of acute and chronic diseases. In many cases, microvessel function is irreversibly compromised, leading to the dysfunction and even death of surrounding tissues. Currently, there are few therapies that directly address the treatment of microvascular insufficiency. Responding to this need, researchers are developing methods to fabricate in vitro blood vessels. Typical strategies include; cellular sodding within polymers and/or biopolymers, the formation of cylindri-cal cellular monolayers around polymer mandrels, and the modification of biocompatible surfaces for cellular adhesion. Using currently available techniques, simple, individual vessel conduits have been engineered with internal diameters down to 150?m. However, no evidence has been provided illustrating the formation of patent, interconnected mi-crovessel networks without the aid of a host circulatory system. In response to this challenge, it is hypothesized that a novel flow-based experimen-tal system will support the in vitro development of three-dimensional microvascular tis-sues. Addressing this hypothesis, the presented work focused on three specific aims: Spe-cific Aim 1. Pattern planar in vitro three-dimensional microvasculatures. Specific Aim 2. Engineer a Dynamic In vitro Perfusion Chamber (DIP Chamber) for microvascular inves-tigation. Specific Aim 3. In vitro perfusion of microvessel fragments within the DIP Chamber. Through the supporting experiments, directed endothelial sprouting from par-ent isolated microvessel fragments was achieved. In addition, patent in vitro microvessel networks were successfully developed. The presented experiments are the first to achieve these experimental results. In addition, the described experimental model will provide a unique method for future investigations of microcirculatory phenomena. Since no exoge-nous growth factors or cell signals were introduced into the constructs, it is believed that this system presents a physiological platform for future investigations into angiogenesis, angioadaptation, and network remodeling. Moreover, this model may offer a useful plat-form for vascular therapeutic testing and a foundation for future tissue engineering applications.
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