Dübendorfer A, Shields G, Sang J H
J Embryol Exp Morphol. 1975 Apr;33(2):487-98.
Embryos of Drosophila melanogaster, 6-8 h after oviposition, were dissociated and the cells cultured in vitro. Besides larval cell types, imaginal disc cells, assembled and growing in bloated monolayered vesicles, were obtained. The cells of these vesicles become competent to differentiate adult structures when treated with alpha-ecdysone or ecdysterone in vitro. Recognizable patterns of the adult fly are not formed though. If metamorphosis of imaginal cell vesicles from in vitro-cultures is induced in vivo by transplantation into host larvae of various ages within the third larval instar, recognizable patterns can differentiate provided the host larva does not metamorphose prior to 2 days after transplantation. The frequency of specific patterns in the implants can be increased by providing 9 days of culture in vivo (adult host flies) before metamorphosis. Passage through the third larval instar is not essential for these cells to produce identifiable patterns since culture in adult flies alone can achieve this. The quality of the differentiated pattern is not correlated with the extent of cell proliferation in the cultured tissues. The problem of pattern specification in vitro and in vivo is discussed.
黑腹果蝇产卵后6至8小时的胚胎被解离,细胞进行体外培养。除了幼虫细胞类型外,还获得了在肿胀的单层囊泡中组装并生长的成虫盘细胞。当在体外用α-蜕皮激素或蜕皮甾酮处理时,这些囊泡的细胞能够分化成成虫结构。不过,并未形成可识别的成年果蝇模式。如果通过移植到第三龄幼虫期内不同年龄的宿主幼虫体内来诱导体外培养的成虫细胞囊泡的变态,只要宿主幼虫在移植后2天之前不变态,就可以分化出可识别的模式。在变态前在体内(成年宿主果蝇)培养9天可以提高植入物中特定模式的频率。对于这些细胞产生可识别的模式而言,经历第三龄幼虫期并非必不可少,因为仅在成年果蝇中培养就能实现这一点。分化模式的质量与培养组织中细胞增殖的程度无关。文中讨论了体外和体内模式指定的问题。