School of Biochemistry, Medical Sciences Building, University Walk, University of Bristol, Bristol BS8 1TD, UK.
Biochem Soc Trans. 2011 Dec;39(6):1597-600. doi: 10.1042/BST20110738.
Angiogenesis is a complex process that involves multiple cellular events. In addition to receiving inputs from a range of stimulatory and inhibitory factors, endothelial cells undergoing angiogenesis make multiple interactions with the extracellular matrix and with other cell types in the stroma. Recreating angiogenesis in vitro is probably an impossible goal; however, a number of assays have been developed that recapitulate many of the key events of the process. These assays are indispensible tools for investigating the signalling pathways that control the formation of new blood vessels. In the present paper, we review the organotypic co-culture assay of angiogenesis - until recently, a comparatively underemployed assay, but one with a number of powerful advantages for angiogenesis research. We give a set of optimized protocols for its use, including protocols for siRNA (small interfering RNA)-based screens, and we discuss appropriate methods for obtaining quantitative data from the assay.
血管生成是一个复杂的过程,涉及多个细胞事件。除了接收来自一系列刺激和抑制因子的输入外,正在进行血管生成的内皮细胞还与细胞外基质以及基质中的其他细胞类型进行多次相互作用。在体外重现血管生成可能是一个不可能实现的目标;然而,已经开发出许多测定法来重现该过程的许多关键事件。这些测定法是研究控制新血管形成的信号通路的不可或缺的工具。在本文中,我们回顾了血管生成的器官型共培养测定法——直到最近,它还是一种相对未被充分利用的测定法,但对于血管生成研究具有许多强大的优势。我们提供了一套经过优化的使用方案,包括基于 siRNA(小干扰 RNA)的筛选方案,并且我们讨论了从测定法中获得定量数据的适当方法。