Kane M T, Norris M, Harrison R A
Department of Molecular Embryology, AFRC Institute of Animal Physiology and Genetics Research, Barbraham, Cambridge, UK.
J Reprod Fertil. 1992 Nov;96(2):617-25. doi: 10.1530/jrf.0.0960617.
The uptake of myo-inositol by preimplantation mouse embryos was investigated using [3H]myo-inositol. Uptake increased about 12-fold between one- and two-cell stages and increased again at the blastocyst stage (> 6-fold compared with the two-cell stage). Uptake at the blastocyst stage was time and temperature dependent; it was stimulated by sodium, inhibited by glucose and appeared to take place mainly via a saturable mechanism. Uptake in the presence of 6.25 mmol inositol l-1 was 1424 fmol inositol per blastocyst per h. About 10% of the [3H]inositol taken up by blastocysts during 8 h in culture was incorporated into lipid. Thin layer chromatography of the lipid showed that most of this inositol was incorporated into lipid material co-migrating with phosphatidylinositol with a small proportion co-migrating with phosphatidylinositol 4-phosphate.
利用[3H]肌醇对植入前小鼠胚胎摄取肌醇的情况进行了研究。摄取量在单细胞期到二细胞期之间增加了约12倍,并在囊胚期再次增加(与二细胞期相比增加了6倍以上)。囊胚期的摄取量与时间和温度有关;它受到钠的刺激,被葡萄糖抑制,并且似乎主要通过一种可饱和机制发生。在存在6.25 mmol肌醇l-1的情况下,每个囊胚每小时摄取的肌醇量为1424 fmol。在培养8小时期间,囊胚摄取的[3H]肌醇中约10%被掺入脂质中。脂质的薄层色谱分析表明,大部分这种肌醇被掺入与磷脂酰肌醇共同迁移的脂质物质中,一小部分与磷脂酰肌醇4-磷酸共同迁移。