血管网
体外
体内
微循环
右旋糖酐
细胞生物学
基质
细胞外基质
化学
生物
生物物理学
生物化学
解剖
免疫学
生物技术
医学
内科学
免疫组织化学
作者
Monica L. Moya,Yu‐Hsiang Hsu,Abraham P. Lee,Christopher C.W. Hughes,Steven C. George
出处
期刊:Tissue Engineering Part C-methods
[Mary Ann Liebert]
日期:2013-01-16
卷期号:19 (9): 730-737
被引量:390
标识
DOI:10.1089/ten.tec.2012.0430
摘要
Replicating in vitro the complex in vivo tissue microenvironment has the potential to transform our approach to medicine and also our understanding of biology. In order to accurately model the 3D arrangement and interaction of cells and extracellular matrix, new microphysiological systems must include a vascular supply. The vasculature not only provides the necessary convective transport of oxygen, nutrients, and waste in 3D culture, but also couples and integrates the responses of organ systems. Here we combine tissue engineering and microfluidic technology to create an in vitro 3D metabolically active stroma (∼1 mm(3)) that, for the first time, contains a perfused, living, dynamic, interconnected human capillary network. The range of flow rate (μm/s) and shear rate (s(-1)) within the network was 0-4000 and 0-1000, respectively, and thus included the normal physiological range. Infusion of FITC dextran demonstrated microvessels (15-50 μm) to be largely impermeable to 70 kDa. Our high-throughput biology-directed platform has the potential to impact a broad range of fields that intersect with the microcirculation, including tumor metastasis, drug discovery, vascular disease, and environmental chemical toxicity.
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