Rylova Svetlana N, Randhawa Paramjeet K, Bautch Victoria L
Department of Biology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Methods Enzymol. 2008;443:103-17. doi: 10.1016/S0076-6879(08)02006-5.
Mouse embryonic stem (ES) cells, derived from the inner cell mass of blastocyst stage embryos, undergo programmed differentiation in vitro to form a primitive vasculature. This programmed differentiation proceeds through similar processes of vasculogenesis and angiogenesis found during early vascular development in vivo. Partially differentiated ES cell clumps or embryoid bodies (EBs) first form blood islands that are subsequently transformed into a network of primitive blood vessels that contain lumens. Therefore, vascular differentiation of ES cells is an ideal model to study and manipulate early vascular development. Here we provide protocols for the routine maintenance of mouse ES cells and in vitro differentiation. We also include protocols for establishing transgenic ES cell lines and visualization of blood vessels by use of endothelial specific molecular markers.
小鼠胚胎干细胞源自囊胚期胚胎的内细胞团,在体外经历程序性分化以形成原始脉管系统。这种程序性分化通过在体内早期血管发育过程中发现的类似血管生成和血管形成过程进行。部分分化的胚胎干细胞团块或胚状体(EBs)首先形成血岛,随后转变为包含管腔的原始血管网络。因此,胚胎干细胞的血管分化是研究和操纵早期血管发育的理想模型。在这里,我们提供了小鼠胚胎干细胞常规培养和体外分化的方案。我们还包括建立转基因胚胎干细胞系以及使用内皮特异性分子标记可视化血管的方案。