Yang Junning, Wu Chuanshen, Stefanescu Ioana, Horowitz Arie
Department of Medicine, Cardeza Vascular Research Center, Sidney Kimmel Medical College, Thomas Jefferson University.
Department of Molecular Cardiology, Cleveland Clinic Foundation.
J Vis Exp. 2017 Apr 22(122):55621. doi: 10.3791/55621.
Mouse embryonic stem cells (ESCs) isolated from the inner mass of the blastocyst (typically at day E3.5), can be used as in vitro model system for studying early embryonic development. In the absence of leukemia inhibitory factor (LIF), ESCs differentiate by default into neural precursor cells. They can be amassed into a three dimensional (3D) spherical aggregate termed embryoid body (EB) due to its similarity to the early stage embryo. EBs can be seeded on fibronectin-coated coverslips, where they expand by growing two dimensional (2D) extensions, or implanted in 3D collagen matrices where they continue growing as spheroids, and differentiate into the three germ layers: endodermal, mesodermal, and ectodermal. The 3D collagen culture mimics the in vivo environment more closely than the 2D EBs. The 2D EB culture facilitates analysis by immunofluorescence and immunoblotting to track differentiation. We have developed a two-step neural differentiation protocol. In the first step, EBs are generated by the hanging-drop technique, and, simultaneously, are induced to differentiate by exposure to retinoic acid (RA). In the second step, neural differentiation proceeds in a 2D or 3D format in the absence of RA.
从囊胚内细胞团分离出的小鼠胚胎干细胞(通常在胚胎第3.5天),可作为研究早期胚胎发育的体外模型系统。在没有白血病抑制因子(LIF)的情况下,胚胎干细胞默认分化为神经前体细胞。由于其与早期胚胎相似,它们可聚集成三维(3D)球形聚集体,称为胚状体(EB)。胚状体可接种在纤连蛋白包被的盖玻片上,在那里它们通过二维(2D)延伸生长而扩展,或植入3D胶原基质中,在那里它们作为球体继续生长,并分化为三个胚层:内胚层、中胚层和外胚层。3D胶原培养比2D胚状体更接近体内环境。2D胚状体培养便于通过免疫荧光和免疫印迹分析来追踪分化。我们已经开发了一种两步神经分化方案。第一步,通过悬滴技术生成胚状体,同时通过暴露于视黄酸(RA)诱导其分化。第二步,在没有RA的情况下,以2D或3D形式进行神经分化。