Van Hoof J, Harrisson F, Vakaet L
Exp Cell Res. 1984 Nov;155(1):278-82. doi: 10.1016/0014-4827(84)90790-0.
A microinjection technique for the chick blastoderm is described. With a micropipette attached to a de Fonbrune micromanipulator, 25-45 nl of a reagent was injected into the entophyllic crescent of a chick blastoderm explanted in vitro according to New [7]. This procedure offers the advantage of eliminating the concentration variability which was observed after subblastodisc injection, and in contrast to the in ovo techniques, it allows one to stage the blastoderms properly. To check its applicability, testicular hyaluronidase was injected. On the basis of morphological and histochemical observations we ascertained that the experimental procedure itself did not interfere with the results. This method may provide a reliable experimental procedure with which to study the interactions between several macromolecules and the tissues during morphogenesis.
本文描述了一种用于鸡胚盘的显微注射技术。通过连接到德方布伦显微操作器的微量移液器,按照纽[7]的方法,将25 - 45 nl的试剂注射到体外培养的鸡胚盘的内胚叶新月区。该方法的优点是消除了胚盘下注射后观察到的浓度变异性,并且与卵内技术相比,它允许对胚盘进行适当的分期。为了检验其适用性,注射了睾丸透明质酸酶。基于形态学和组织化学观察,我们确定实验过程本身不会干扰结果。该方法可能为研究形态发生过程中几种大分子与组织之间的相互作用提供一种可靠的实验方法。