Nikitenko L, Morgan G, Kolesnikov S I, Wooding F B
The Babraham Institute, Cambridge United Kingdom.
J Histochem Cytochem. 1998 May;46(5):679-88. doi: 10.1177/002215549804600513.
The fetus must transport considerable and increasing amounts of calcium across the placental trophoblast epithelium to support growth and development and bone formation. Active calcium transport across epithelia has been shown to correlate with calbindin D9k or 28k content. This study examined the distribution of calbindin D9k (9CBP) protein and mRNA during pregnancy in the bovine placenta to determine its possible role in calcium transport in this system. The immunocytochemical results show 9CBP in an increasing percentage of interplacentomal uninucleate trophoblast cells until, at term, all show a level at least eight times that of any other placental cell. There is a similar, although smaller, rise in their 9CBP mRNA content. The mature interplacentomal binucleate cell ( approximately 5% of the total) contains no 9CBP at any stage of pregnancy. In interplacentomal uterine epithelium, 9CBP protein and mRNA decrease to zero in late pregnancy but the glands maintain constant low levels throughout. In the placentome trophoblast, uninucleate cells show insignificant amounts but binucleate cells (15-20% of the total trophoblast cells) contain considerable levels of both 9CBP protein and mRNA, as do all the uninucleate uterine epithelial cells. The placentomal binucleate cells show peak values at mid-pregnancy; the placentomal uterine epithelium shows only small changes in levels in the second half of pregnancy. Increase in fetal calcium demand in the second half of pregnancy therefore correlates with a major increase in 9CBP only in the interplacentomal trophoblast, as we have also shown in the sheep and goat, indicating an important role for this region in active calcium transport by the ruminant placenta. The 9CBP is distributed uniformly in the cytosol and nucleoplasm, supporting a role in facilitated diffusion of calcium through the cell rather than a vesicular shuttle system.
胎儿必须通过胎盘滋养层上皮转运大量且不断增加的钙,以支持生长发育和骨骼形成。上皮细胞的主动钙转运已被证明与钙结合蛋白D9k或28k的含量相关。本研究检测了牛胎盘妊娠期间钙结合蛋白D9k(9CBP)蛋白和mRNA的分布,以确定其在该系统钙转运中的可能作用。免疫细胞化学结果显示,胎盘小叶间单核滋养层细胞中9CBP的比例不断增加,直至足月时,所有细胞的水平至少是其他任何胎盘细胞的八倍。它们的9CBP mRNA含量也有类似的升高,尽管幅度较小。成熟的胎盘小叶间双核细胞(约占总数的5%)在妊娠的任何阶段都不含9CBP。在胎盘小叶间子宫上皮中,9CBP蛋白和mRNA在妊娠后期降至零,但腺体在整个过程中保持恒定的低水平。在胎盘绒毛叶滋养层中,单核细胞含量极少,但双核细胞(占滋养层细胞总数的15 - 20%)含有大量的9CBP蛋白和mRNA,所有单核子宫上皮细胞也是如此。胎盘绒毛叶双核细胞在妊娠中期显示峰值;胎盘绒毛叶子宫上皮在妊娠后半期水平仅略有变化。因此,妊娠后半期胎儿钙需求的增加仅与胎盘小叶间滋养层中9CBP的大幅增加相关,正如我们在绵羊和山羊中所显示的那样,这表明该区域在反刍动物胎盘的主动钙转运中起重要作用。9CBP均匀分布于细胞质和核质中,支持其在促进钙通过细胞扩散而非囊泡穿梭系统中发挥作用。