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体外培养的胚胎期鸡胚血液中原始生殖细胞的运动及扫描电子显微镜观察

Locomotion and scanning electron microscopic observations of primordial germ cells from the embryonic chick blood in vitro.

作者信息

Kuwana T, Fujimoto T

出版信息

Anat Rec. 1984 Jul;209(3):337-43. doi: 10.1002/ar.1092090312.

Abstract

The locomotion of chick primordial germ cells (PGCs) in vitro was observed using 16-mm time-lapse microcinematography and 35-mm time-lapse film. The PGCs isolated from circulating blood of stage 14 to 16 embryos (Hamburger and Hamilton, 1951) were cultured on a substrate of mesenchymal feeder cells obtained from the dorsal mesentery of stage 40 embryos, using modified medium 199 containing 10% fetal calf serum. The PGCs were found to move actively and to show a tendency to move along the longer axis of the underlying cells. The velocity of PGC locomotion averaged 26 micron/hr and reached 58 micron/hr as a maximum. After observation, the PGCs were processed for scanning electron microscopy. They had a considerable number of microvilli about 0.2 micron in thickness and some cytoplasmic blebs on their surfaces. It was observed that the PGCs in the migrating phase adhered to the substrate with its filopodia only at the leading edge, while a large part of the cell appeared to be apart from the substrate.

摘要

利用16毫米延时显微电影摄影术和35毫米延时胶片观察了鸡原始生殖细胞(PGCs)在体外的运动。从第14至16期胚胎(Hamburger和Hamilton,1951)的循环血液中分离出的PGCs,使用含有10%胎牛血清的改良培养基199,培养在从第40期胚胎背系膜获得的间充质饲养层细胞的底物上。发现PGCs能活跃移动,并表现出沿下层细胞长轴移动的趋势。PGCs移动速度平均为26微米/小时,最高可达58微米/小时。观察后,对PGCs进行扫描电子显微镜处理。它们表面有大量厚度约为0.2微米的微绒毛和一些细胞质小泡。观察到处于迁移阶段的PGCs仅在前缘通过丝状伪足附着于底物,而细胞的大部分似乎与底物分离。

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