Molls M, Weissenborn U, Streffer C
Strahlentherapie. 1982 Aug;158(8):504-12.
1-or 2-cell mouse embryos were X-irradiated with 1.88 Gy. At irradiation time both pronuclei of each 1-cell embryo (see introduction) had a haploid DNA-amount and were in G1-phase. In contrast the cell nuclei of the 2-cell embryos had a tetraploid DNA-amount and were in late G2. DNA-amount and the cell cycle phases respectively were determined cytofluorometrically. The blastocyst formation was more impaired after irradiation of 1-cell embryos (28%) than 2-cell embryos (73%; controls: 100%). Cell death, which was observed in the cell proliferation investigations, should be the most important reason for the impaired early embryonic development. The different extent of cell death can be explained with the different amount of micronucleus formation. This chromosomal damage, which leads to a hypoploid DNA-amount of the cell nuclei, was more bulky after irradiation of 1-cell embryos than 2-cell embryos. Mechanisms which could cause a higher micronucleus formation after irradiation of haploid cell nuclei (pronuclei) in G1-phase than after irradiation of tetraploid cell nuclei in G2-phase are discussed.
将1 - 2细胞期的小鼠胚胎用1.88 Gy的X射线进行照射。在照射时,每个1细胞期胚胎的两个原核(见引言)都具有单倍体DNA含量,且处于G1期。相比之下,2细胞期胚胎的细胞核具有四倍体DNA含量,且处于G2晚期。分别通过细胞荧光光度法测定DNA含量和细胞周期阶段。1细胞期胚胎照射后囊胚形成的受损程度(28%)比2细胞期胚胎(73%;对照组:100%)更大。在细胞增殖研究中观察到的细胞死亡应该是早期胚胎发育受损的最重要原因。细胞死亡程度的差异可以用微核形成量的不同来解释。这种导致细胞核DNA含量亚倍体化的染色体损伤,在1细胞期胚胎照射后比2细胞期胚胎更严重。文中讨论了可能导致G1期单倍体细胞核(原核)照射后比G2期四倍体细胞核照射后微核形成更多的机制。