Stanirowski Paweł Jan, Szukiewicz Dariusz, Majewska Agata, Wątroba Mateusz, Pyzlak Michał, Bomba-Opoń Dorota, Wielgoś Mirosław
1st Department of Obstetrics and Gynecology, Medical University of Warsaw, 02-015 Warsaw, Poland.
Department of Biophysics, Physiology and Pathophysiology, Faculty of Health Sciences, Medical University of Warsaw, 02-004 Warsaw, Poland.
J Clin Med. 2021 Dec 13;10(24):5833. doi: 10.3390/jcm10245833.
Placental transfer of glucose constitutes one of the major determinants of the intrauterine foetal growth. The objective of the present study was to evaluate the expression of glucose transporter proteins GLUT-1, GLUT-3, GLUT-8 and GLUT-12 in the placenta of macrosomic, small-for-gestational-age (SGA) and growth-restricted foetuses (FGR). A total of 70 placental tissue samples were collected from women who delivered macrosomic ≥4000 g ( = 26), SGA ( = 11), growth-restricted ( = 13) and healthy control neonates ( = 20). Computer-assisted quantitative morphometry of stained placental sections was performed to determine the expression of selected GLUT proteins. Immunohistochemical staining identified the presence of all glucose transporters in the placental tissue. Quantitative morphometric analysis performed for the vascular density-matched placental samples revealed a significant decrease in GLUT-1 and increase in GLUT-3 protein expression in pregnancies complicated by FGR as compared to other groups ( < 0.05). In addition, expression of GLUT-8 was significantly decreased among SGA foetuses ( < 0.05). No significant differences in GLUTs expression were observed in women delivering macrosomic neonates. In the SGA group foetal birth weight (FBW) was negatively correlated with GLUT-3 (rho = -0.59, < 0.05) and positively with GLUT-12 (rho = 0.616, < 0.05) placental expression. In addition, a positive correlation between FBW and GLUT-12 expression in the control group (rho = 0.536, < 0.05) was noted. In placentas derived from FGR-complicated pregnancies the expression of two major glucose transporters GLUT-1 and GLUT-3 is altered. On the contrary, idiopathic foetal macrosomia is not associated with changes in the placental expression of GLUT-1, GLUT-3, GLUT-8 and GLUT-12 proteins.
葡萄糖的胎盘转运是胎儿宫内生长的主要决定因素之一。本研究的目的是评估葡萄糖转运蛋白GLUT-1、GLUT-3、GLUT-8和GLUT-12在巨大儿、小于胎龄儿(SGA)和生长受限胎儿(FGR)胎盘中的表达。共收集了70份胎盘组织样本,这些样本来自分娩巨大儿(≥4000g,n = 26)、SGA(n = 11)、生长受限儿(n = 13)和健康对照新生儿(n = 20)的女性。对染色的胎盘切片进行计算机辅助定量形态测量,以确定所选GLUT蛋白的表达。免疫组织化学染色确定了胎盘组织中所有葡萄糖转运蛋白的存在。对血管密度匹配的胎盘样本进行的定量形态分析显示,与其他组相比,FGR合并妊娠中GLUT-1表达显著降低,GLUT-3蛋白表达增加(P < 0.05)。此外,SGA胎儿中GLUT-8的表达显著降低(P < 0.05)。分娩巨大儿的女性中未观察到GLUTs表达的显著差异。在SGA组中,胎儿出生体重(FBW)与GLUT-3胎盘表达呈负相关(rho = -0.59,P < 0.05),与GLUT-12呈正相关(rho = 0.616,P < 0.05)。此外,在对照组中FBW与GLUT-12表达呈正相关(rho = 0.536,P < 0.05)。在FGR合并妊娠的胎盘中,两种主要葡萄糖转运蛋白GLUT-1和GLUT-3的表达发生改变。相反,特发性胎儿巨大症与GLUT-1、GLUT-3、GLUT-8和GLUT-12蛋白的胎盘表达变化无关。