Ito K, Takeuchi T
J Embryol Exp Morphol. 1984 Dec;84:49-62.
A culture method for neural crest cells of mouse embryo is described. Trunk neural tubes were dissected from 9-day mouse embryos and explanted in culture dishes. The developmental potential of mouse neural crest in vitro was shown to be essentially similar to that of avian neural crest. In the mouse, however, melanocytes always appeared in association with the epithelial sheet close to the explant. Neural crest cells surrounding the epithelial sheet, which probably migrated from the neural tubes in the early culture phase, never differentiated into melanocytes. The bimodal behaviour of mouse crest cells seems to be due to the heterogenous potency of the crest cells and the interaction of these cells with the surrounding microenvironment. This culture system is well suited for various experiments including the analysis of gene control on the differentiation of neural crest cells.
描述了一种小鼠胚胎神经嵴细胞的培养方法。从9日龄小鼠胚胎中分离出躯干神经管,并接种于培养皿中。结果表明,小鼠神经嵴在体外的发育潜能与禽类神经嵴基本相似。然而,在小鼠中,黑素细胞总是与靠近外植体的上皮片相关联出现。围绕上皮片的神经嵴细胞,可能在培养早期从神经管迁移而来,从未分化为黑素细胞。小鼠嵴细胞的双峰行为似乎是由于嵴细胞的异质性潜能以及这些细胞与周围微环境的相互作用。这种培养系统非常适合各种实验,包括分析神经嵴细胞分化的基因控制。