Johansson M, Glazier J D, Sibley C P, Jansson T, Powell T L
Perinatal Center, Department of Physiology and Pharmacology, Göteborg University, S-405 30 Göteborg, Sweden.
J Clin Endocrinol Metab. 2002 Dec;87(12):5686-94. doi: 10.1210/jc.2002-020214.
Regulation of syncytiotrophoblast intracellular pH is critical to optimum enzymatic and transport functions of the placenta. Previous studies of Na(+)/H(+) exchanger (NHE) activity in the placenta from pregnancies complicated by intrauterine growth restriction (IUGR) have produced conflicting results. The possible role of altered placental pH regulation in the development of acidosis in some fetuses subjected to IUGR remains to be fully established. We investigated the activity and protein expression of the NHE in syncytiotrophoblast microvillous (MVM) plasma membranes isolated from preterm and term placentas obtained from uncomplicated and IUGR pregnancies. Western blotting showed that the expression of NHE isoforms 1, 2, and 3 was approximately 10-fold greater in MVM than in basal plasma membrane (BM). Immunohistochemistry localized NHE-1 and NHE-2 to MVM and BM and NHE-3 to the MVM, BM, and cytoplasm of the syncytiotrophoblast. NHE-1 expression in MVM from preterm IUGR placentas was reduced by 55%, compared with gestational age-matched controls (P < 0.05, n = 6 and n = 16, respectively), whereas NHE-1 expression was unaltered in term IUGR placentas (n = 8). The activity (amiloride-sensitive Na(+) uptake) of NHE in MVM from IUGR preterm placentas was reduced by 48% (P < 0.05, n = 6). In contrast, MVM NHE activity was unchanged in term IUGR (n = 7). Using Northern blotting, no difference could be demonstrated in NHE-1 mRNA expression between IUGR and control groups. The reduced activity and expression of NHE in MVM of preterm IUGR placentas may compromise placental function and may contribute to the development of fetal acidosis in preterm IUGR fetuses.
合体滋养层细胞内pH值的调节对于胎盘最佳的酶促功能和转运功能至关重要。先前关于宫内生长受限(IUGR)妊娠胎盘钠氢交换体(NHE)活性的研究结果相互矛盾。胎盘pH调节改变在一些IUGR胎儿酸中毒发展中的可能作用仍有待充分明确。我们研究了从无并发症和IUGR妊娠的早产和足月胎盘分离的合体滋养层微绒毛(MVM)质膜中NHE的活性和蛋白表达。蛋白质印迹法显示,NHE亚型1、2和3在MVM中的表达比在基底质膜(BM)中大约高10倍。免疫组织化学将NHE-1和NHE-2定位于MVM和BM,将NHE-3定位于合体滋养层的MVM、BM和细胞质。与胎龄匹配的对照组相比,早产IUGR胎盘MVM中NHE-1的表达降低了55%(P<0.05,分别为n = 6和n = 16),而足月IUGR胎盘(n = 8)中NHE-1的表达未改变。IUGR早产胎盘MVM中NHE的活性(氨氯地平敏感的钠摄取)降低了48%(P<0.05,n = 6)。相比之下,足月IUGR胎盘(n = 7)的MVM中NHE活性未改变。使用Northern印迹法,IUGR组和对照组之间在NHE-1 mRNA表达上未显示出差异。早产IUGR胎盘MVM中NHE活性和表达的降低可能损害胎盘功能,并可能导致早产IUGR胎儿发生胎儿酸中毒。