Luo Jiankai, Yan Xin, Lin Juntang, Rolfs Arndt
Albrecht-Kossel-Institute for Neuroregeneration, School of Medicine, University of Rostock.
J Vis Exp. 2012 Jul 27(65):4078. doi: 10.3791/4078.
The chicken embryo provides an excellent model system for studying gene function and regulation during embryonic development. In ovo electroporation is a powerful method to over-express exogenous genes or down-regulate endogenous genes in vivo in chicken embryos(1). Different structures such as DNA plasmids encoding genes(2-4), small interfering RNA (siRNA) plasmids(5), small synthetic RNA oligos(6), and morpholino antisense oligonucleotides(7) can be easily transfected into chicken embryos by electroporation. However, the application of in ovo electroporation is limited to embryos at early incubation stages (younger than stage HH20--according to Hamburg and Hamilton)(8) and there are some disadvantages for its application in embryos at later stages (older than stage HH22--approximately 3.5 days of development). For example, the vitelline membrane at later stages is usually stuck to the shall membrane and opening a window in the shell causes rupture of the vessels, resulting in death of the embryos; older embryos are covered by vitelline and allantoic vessels, where it is difficult to access and manipulate the embryos; older embryos move vigorously and is difficult to control the orientation through a relatively small window in the shell. In this protocol we demonstrate an ex ovo electroporation method for gene transfer into chicken embryos at late stages (older than stage HH22). For ex ovo electroporation, embryos are cultured in Petri dishes(9) and the vitelline and allantoic vessels are widely spread. Under these conditions, the older chicken embryos are easily accessed and manipulated. Therefore, this method overcomes the disadvantages of in ovo electroporation applied to the older chicken embryos. Using this method, plasmids can be easily transfected into different parts of the older chicken embryos(10-12).
鸡胚为研究胚胎发育过程中的基因功能和调控提供了一个出色的模型系统。卵内电穿孔是一种在鸡胚体内过表达外源基因或下调内源基因的强大方法(1)。不同结构,如编码基因的DNA质粒(2 - 4)、小干扰RNA (siRNA)质粒(5)、小合成RNA寡核苷酸(6)和吗啉代反义寡核苷酸(7),都可以通过电穿孔轻松转染到鸡胚中。然而,卵内电穿孔的应用仅限于孵化早期的胚胎(根据汉堡和汉密尔顿标准,小于HH20期)(8),在后期胚胎(大于HH22期 - 约发育3.5天)中应用存在一些缺点。例如,后期的卵黄膜通常与壳膜粘连,在蛋壳上开窗会导致血管破裂,从而导致胚胎死亡;较大的胚胎被卵黄和尿囊血管覆盖,难以接近和操作;较大的胚胎活动剧烈,难以通过蛋壳上相对较小的窗口控制其方向。在本方案中,我们展示了一种用于将基因导入后期鸡胚(大于HH22期)的卵外电穿孔方法。对于卵外电穿孔,胚胎在培养皿中培养(9),卵黄和尿囊血管广泛展开。在这些条件下,较老的鸡胚易于接近和操作。因此,该方法克服了将卵内电穿孔应用于较老鸡胚的缺点。使用这种方法,可以轻松地将质粒转染到较老鸡胚的不同部位(10 - 12)。