Department of Obstetrics and Gynecology, University of Colorado Denver and Health Sciences Center, Aurora, Colorado, USA.
Biol Reprod. 2012 Mar 30;86(3):94. doi: 10.1095/biolreprod.111.094797. Print 2012 Mar.
TonEBP/NFAT5 (the tonicity-responsive enhancer binding protein/nuclear factor of activated T cells) modulates cellular response to osmotic changes by accumulating inositol and sorbitol inside the cells. Our objective was to assess placental osmolytes, TonEBP/NFAT5 RNA and protein expression, and signaling molecules across gestation between control and intrauterine growth restriction (IUGR) ovine pregnancies. Pregnant sheep were placed in hyperthermic conditions to induce IUGR. Placental tissues were collected at 55, 95, and 130 days gestational age (dGA) to measure inositol, sorbitol, TonEBP/NFAT5 (NFAT5), sodium-dependent myo-inositol transporter (SMIT; official symbol SLC5A3), aldose reductase (AR), and NADPH (official symbol DE-CR1). Placental weight was reduced in IUGR compared to controls at 95 and 130 dGA. Osmolyte concentrations were similar between control and IUGR placentas, but both groups demonstrated a significant decrease in inositol concentration and an increase in sorbitol concentration with advancing gestation. Cytosolic NFAT5 protein decreased significantly from 55 to 95 dGA in both groups, and nuclear NFAT5 protein increased only at 130 dGA in the IUGR group, but no differences were seen between groups for either cytosolic or nuclear NFAT5 protein concentrations. DE-CR1 concentrations were similar between groups and increased significantly with advancing gestational age. AR was lowest at 55dGA, and SLC5A3 increased with advancing gestational age. We conclude that both placental osmolytes inositol and sorbitol (and their corresponding proteins SLC5A3 and AR) change with gestational age and are regulated, at least in part, by NFAT5 and DE-CR1 (NADPH). The inverse relationship between each osmolyte across gestation (e.g., inositol higher in early gestation and sorbitol higher in late gestation) may reflect nutritional needs that change across gestation.
TonEBP/NFAT5(渗透压应答增强子结合蛋白/激活 T 细胞核因子)通过在细胞内积累肌醇和山梨醇来调节细胞对渗透压变化的反应。我们的目的是评估控制和宫内生长受限(IUGR)绵羊妊娠之间妊娠过程中的胎盘渗透物、TonEBP/NFAT5 RNA 和蛋白表达以及信号分子。将妊娠绵羊置于高温条件下以诱导 IUGR。在 55、95 和 130 天妊娠龄(dGA)收集胎盘组织,以测量肌醇、山梨醇、TonEBP/NFAT5(NFAT5)、钠依赖性肌醇转运蛋白(SMIT;官方符号 SLC5A3)、醛糖还原酶(AR)和 NADPH(官方符号 DE-CR1)。与对照组相比,IUGR 组在 95 和 130 dGA 时胎盘重量减轻。渗透物浓度在对照组和 IUGR 胎盘之间相似,但两组随着妊娠的进展,肌醇浓度显著降低,山梨醇浓度增加。在两组中,细胞质 NFAT5 蛋白从 55 至 95 dGA 显著下降,而核 NFAT5 蛋白仅在 IUGR 组的 130 dGA 时增加,但两组之间细胞质或核 NFAT5 蛋白浓度均无差异。DE-CR1 浓度在两组之间相似,随着妊娠龄的增加而显著增加。AR 在 55dGA 时最低,SLC5A3 随妊娠龄增加而增加。我们得出结论,胎盘渗透物肌醇和山梨醇(及其相应的蛋白 SLC5A3 和 AR)随妊娠龄而变化,至少部分受 NFAT5 和 DE-CR1(NADPH)调节。妊娠过程中每种渗透物之间的反比关系(例如,早期妊娠时肌醇较高,晚期妊娠时山梨醇较高)可能反映了妊娠过程中变化的营养需求。