Nakashima K, Ninomiya H, Fujiki Y
Experientia. 1984 Sep 15;40(9):924-9. doi: 10.1007/BF01946441.
Mouse embryos explanted at various stages during neurulation were cultured for 20-28 h in the presence of 25-900 micrograms/ml of 5-bromodeoxyuridine (BUdR). BUdR strongly inhibited closure of the cranial neural tube, which was found to be stage-dependent. When mouse embryos were exposed to BUdR after development of the concave curvature in the neuroepithelium of the midbrain to the upper hindbrain regions, they became insensitive to the drug-induced open cranial neural tube. Histological observations showed that BUdR interfered with interkinetic migration and cytokinesis of the neuroepithelial cells. These cellular abnormalities were not dependent on the morphological development of the cranial neural folds. The 3H-BUdR experiment confirmed that the label was mostly incorporated into the DNA fraction.
在神经胚形成的不同阶段取出的小鼠胚胎,在含有25 - 900微克/毫升5-溴脱氧尿苷(BUdR)的条件下培养20 - 28小时。BUdR强烈抑制颅神经管的闭合,且发现这种抑制具有阶段依赖性。当中脑至上后脑区域神经上皮的凹曲率发育完成后,将小鼠胚胎暴露于BUdR时,它们对药物诱导的开放性颅神经管变得不敏感。组织学观察表明,BUdR干扰了神经上皮细胞的动间迁移和胞质分裂。这些细胞异常并不依赖于颅神经褶的形态发育。3H - BUdR实验证实,标记物大多掺入了DNA部分。