Matsuda M, Yasutomi M
Department of Embryology, Institute for Development Research, Aichi, Japan.
Anat Embryol (Berl). 1992;185(3):217-23. doi: 10.1007/BF00211820.
Head-fold stage rat embryos (9.5 days of gestation) were cultured for 48 h in rat serum with or without 0.8 microM 5-azacytidine. Incomplete closure of the cephalic neural tube was observed in 5-azacytidine-treated embryos cultured for 48 h (25-somite stage). Control embryos showed complete fusion of cephalic neural folds at 33 h (16-somite stage) in culture. Drug administration or removal experiments revealed that embryos were sensitive to 5-azacytidine during 6-12 h of culture (three to five somite stages). Electron microscopical studies indicated that the arrangement and fine structure of cephalic neuroepithelial cells were almost the same in control and treated embryos. There was no significant difference in DNA and protein contents between control and treated embryos cultured for 36 h. Immunocytochemical observations using 5-methylcytosine-specific antibody revealed that the staining of neuroepithelial cells in the median part of the transversely sectioned cephalic neural plate, and of mesenchymal cells near the apices of the plate, was suppressed by 5-azacytidine. These results suggest that DNA methylation of these cells plays an important role in closure of the cephalic neural tube.
头部折叠期大鼠胚胎(妊娠9.5天)在含有或不含有0.8微摩尔5-氮杂胞苷的大鼠血清中培养48小时。在培养48小时(25体节期)的经5-氮杂胞苷处理的胚胎中观察到头部神经管闭合不全。对照胚胎在培养33小时(16体节期)时显示头部神经褶完全融合。给药或去除实验表明,胚胎在培养6-12小时(三至五体节期)期间对5-氮杂胞苷敏感。电子显微镜研究表明,对照胚胎和处理过的胚胎中头部神经上皮细胞的排列和精细结构几乎相同。培养36小时的对照胚胎和处理过的胚胎之间的DNA和蛋白质含量没有显著差异。使用5-甲基胞嘧啶特异性抗体的免疫细胞化学观察显示,5-氮杂胞苷抑制了横切头部神经板中部神经上皮细胞以及板尖附近间充质细胞的染色。这些结果表明,这些细胞的DNA甲基化在头部神经管闭合中起重要作用。