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大鼠主动脉环模型中的三维体外血管生成

Three-dimensional in vitro anglogenesis in the rat aortic ring model.

作者信息

West David C, Burbridge Mike F

机构信息

School of Biological Sciences, University of Liverpool, Liverpool, UK.

出版信息

Methods Mol Biol. 2009;467:189-210. doi: 10.1007/978-1-59745-241-0_11.

Abstract

Angiogenesis is a complex sequential process involving endothelial activation, basement membrane degradation, endothelial sprouting from the parent vessel, invasion of the extracellular matrix, endothelial proliferation, vessel elongation, branching, anastomosis, increases in vessel diameter, basement membrane formation, pericyte acquisition, and remodelling. Most in vitro angiogenesis assays are two-dimensional and measure only one facet of this process, generally endothelial proliferation, migration, or tube formation. The two-dimensional nature of the assays also ignores the differences in endothelial phenotype seen in three-dimensional models and in vivo. The in vitro serum-free three-dimensional rat aortic model closely approximates the complexities of angiogenesis in vivo, from endothelial activation to pericyte acquisition and remodelling, and most of these can be quantified by image analysis, immunohistochemistry, and biochemical analysis. It is easily manipulated using molecular biological intervention or exogenous inhibitors and activators in a relatively controlled system.

摘要

血管生成是一个复杂的连续过程,涉及内皮细胞激活、基底膜降解、内皮细胞从母血管发芽、侵入细胞外基质、内皮细胞增殖、血管伸长、分支、吻合、血管直径增加、基底膜形成、周细胞募集和重塑。大多数体外血管生成试验是二维的,仅测量该过程的一个方面,通常是内皮细胞增殖、迁移或管形成。这些试验的二维性质也忽略了在三维模型和体内观察到的内皮细胞表型差异。体外无血清三维大鼠主动脉模型非常接近体内血管生成的复杂性,从内皮细胞激活到周细胞募集和重塑,其中大部分可以通过图像分析、免疫组织化学和生化分析进行量化。在相对可控的系统中,使用分子生物学干预或外源性抑制剂和激活剂很容易对其进行操作。

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