Wiley L M
J Exp Zool. 1978 Oct;206(1):13-6. doi: 10.1002/jez.1402060103.
Mouse ICM's that were isolated from blastocysts by immunosurgery and subsequently cultured for four to five days were tested for their ability to form trophoblast giant cells (TGC's) in vitro. The cores were isolated from such ICM's by a second immunosurgery and cultured for 7 to 14 days. After two days of culture a variable percentage (30%--90%) of the ICM cores produced outgrowths containing cells that resembled those of cultured ectoplacental cone. Then the outgrowths became amitotic and produced vascuolated cells that enlarged to dimensions of 200 X 375 micrometer with nuclei as large as 53 micrometer in diameter. The time course of their development from the ICM cores, their morphology and their nuclear diameters suggest that these large cells were TGC's.
通过免疫手术从囊胚中分离出的小鼠内细胞团(ICM),随后培养四到五天,检测其在体外形成滋养层巨细胞(TGC)的能力。通过第二次免疫手术从这些ICM中分离出核心,并培养7至14天。培养两天后,不同比例(30% - 90%)的ICM核心产生含有类似培养的外胎盘锥细胞的生长物。然后这些生长物停止有丝分裂,产生空泡化细胞,其大小扩大到200×375微米,细胞核直径达53微米。它们从ICM核心发育的时间进程、形态和核直径表明这些大细胞是TGC。