Barcroft L C, Gill S E, Watson A J
Departments of Obstetrics and Gynaecology and Physiology, The University of Western Ontario, London, Ontario N6A 5C1, Canada.
Reproduction. 2002 Sep;124(3):387-97.
Expression and activity of the Na-K-ATPase within the basolateral membrane domains of the trophectoderm epithelium provide the driving force for accumulation of Na(+) and Cl(-) across the nascent epithelium, mediating fluid movement into the forming blastocoel. Within the trophectoderm of the bovine blastocyst, multiple isozymes of the Na-K-ATPase are expressed. Immunolocalization has demonstrated that the alpha1-isozyme localizes within the basolateral membrane, whereas the alpha 3-isozyme localizes to the apical cell margins. Gene-specific RT-PCR and wholemount indirect immunofluorescence confocal laser scanning microscopy were used to examine expression of the Na-K-ATPase gamma-subunit (a regulatory subunit of the Na-K-ATPase) throughout development of bovine preattachment embryos in vitro. Expression of mRNA transcripts for the gamma-subunit was detected throughout bovine pre-attachment development from the fertilized one-cell embryo to the blastocyst stage. A similar pattern of expression was also observed for gamma-subunit protein, and immunofluorescence was detected within the membranes of embryonic blastomeres at all stages of development. In contrast to the expression patterns observed for the alpha-subunits, gamma-subunit proteins were detected in both the basolateral and apical cell margins of the trophectoderm, and surrounding all cells of the inner cell mass. Co-localization studies demonstrated that gamma-subunit peptides are co-expressed with the alpha1-subunit in the basolateral domains of the trophectoderm. These results indicate a role for the gamma-subunit of the Na-K-ATPase in modulating Na(+)-pump activity in both apical and basolateral margins of the trophectoderm during formation and expansion of the bovine blastocyst, and adds a further level of complexity to Na(+)-pump regulation of cavitation.
滋养外胚层上皮基底外侧膜结构域内钠钾ATP酶的表达及活性为钠(Na⁺)和氯(Cl⁻)跨新生上皮的积累提供驱动力,介导液体进入正在形成的囊胚腔。在牛囊胚的滋养外胚层内,表达了钠钾ATP酶的多种同工酶。免疫定位表明,α1同工酶定位于基底外侧膜,而α3同工酶定位于顶端细胞边缘。利用基因特异性逆转录聚合酶链反应(RT-PCR)和整装间接免疫荧光共聚焦激光扫描显微镜,检测体外培养的牛着床前胚胎发育过程中钠钾ATP酶γ亚基(钠钾ATP酶的一种调节亚基)的表达。从受精的单细胞胚胎到囊胚阶段的整个牛着床前发育过程中,均检测到γ亚基mRNA转录本的表达。γ亚基蛋白也观察到类似的表达模式,并且在发育各阶段的胚胎卵裂球膜内均检测到免疫荧光。与α亚基的表达模式不同,γ亚基蛋白在滋养外胚层的基底外侧和顶端细胞边缘以及内细胞团的所有细胞周围均有检测到。共定位研究表明,γ亚基肽与α1亚基在滋养外胚层的基底外侧结构域共表达。这些结果表明,在牛囊胚形成和扩张过程中,钠钾ATP酶γ亚基在调节滋养外胚层顶端和基底外侧边缘的钠泵活性中发挥作用,并为钠泵对空泡化的调节增加了另一层复杂性。