Johansson S, Wide M
Department of Animal Development and Genetics, Uppsala, Sweden.
Anat Embryol (Berl). 1994 Sep;190(3):287-96. doi: 10.1007/BF00234306.
The development of the rodent chorio-allantoic placenta is a complicated process that results in the formation of a transport system capable of sustaining embryonic and fetal growth and development. Intimately linked to this process is alkaline phosphatase (AP), a cell-surface glycoprotein that possibly functions as a transport protein. In the present study, we have mapped the location of AP-expressing cells in the mouse utero-placental unit during the development of the chorio-allantoic placenta by use of enzyme histochemistry and in situ hybridization histochemistry. We found that at implantation the expression of the tissue non-specific AP (TNAP) gene is located exclusively in the decidua and that most of this decidual expression ceases as the placenta starts to form. One exception is a mesometrially located marginal zone of the decidua, which continues to express the TNAP gene until day 12 and the active protein until at least day 16. Trophoblasts of the chorion already express AP before the time of fusion with the ectoplacental cone, after which AP is expressed by trophoblasts of the resulting ectoplacental plate. AP expression in the mature chorio-allantoic placenta is localized in the placental labyrinth and spongy zones. In the latter zone, expression ceases on about day 14. Giant trophoblasts start to express AP on about day 10, with some cells still positive for AP at day 16. The yolk sac does not express AP at any developmental stage. The results show that AP expression during placental development is neither restricted to cells known to be involved in transport, nor expressed in all cells thought to be involved in this transport. This may indicate that AP is not merely a transport protein but has additional functions.
啮齿动物绒毛膜尿囊胎盘的发育是一个复杂的过程,最终形成一个能够维持胚胎和胎儿生长发育的转运系统。与这个过程密切相关的是碱性磷酸酶(AP),一种细胞表面糖蛋白,可能作为一种转运蛋白发挥作用。在本研究中,我们利用酶组织化学和原位杂交组织化学技术,绘制了绒毛膜尿囊胎盘发育过程中小鼠子宫胎盘单位中表达AP的细胞的位置。我们发现,在植入时,组织非特异性AP(TNAP)基因的表达仅位于蜕膜,并且随着胎盘开始形成,大部分蜕膜表达停止。一个例外是蜕膜的位于子宫系膜的边缘区,该区域持续表达TNAP基因直至第12天,活性蛋白至少持续表达至第16天。绒毛膜的滋养层在与外胎盘锥融合之前就已经表达AP,融合后,由此产生的外胎盘板的滋养层表达AP。成熟绒毛膜尿囊胎盘中的AP表达定位于胎盘迷路和海绵区。在后者区域,表达在大约第14天停止。巨大滋养层在大约第10天开始表达AP,在第16天一些细胞仍为AP阳性。卵黄囊在任何发育阶段都不表达AP。结果表明,胎盘发育过程中的AP表达既不限于已知参与转运的细胞,也不在所有被认为参与这种转运的细胞中表达。这可能表明AP不仅仅是一种转运蛋白,还具有其他功能。