Effect of Hypoxia on Glucose Transporter 1 and 3 Gene Expression in Placental Mesenchymal Stem Cells Derived from Growth-Restricted Fetuses

被引:4
|
作者
Chang, Yao-Lung [1 ]
Chang, Shuenn-Dyh [1 ]
Chao, An-Shine [1 ]
Sieber, Martin [2 ]
Tsai, Chia-Lung [3 ]
Cheng, Po-Jen [1 ]
机构
[1] Chang Gung Univ, Chang Gung Mem Hosp, Coll Med, Dept Obstet & Gynecol, Taoyuan 333, Taiwan
[2] BIONET Corp, 28,Ln 36,Xinhu 1st Rd, Taipei 114, Taiwan
[3] Chang Gung Mem Hosp, Genom Med Res Core Lab, Taoyuan 333, Taiwan
关键词
glucose transporter; intrauterine growth restriction; hypoxia; placenta; mesenchymal stem cells; MONOCHORIONIC TWIN PREGNANCIES; GLUCOSE TRANSPORTERS; HUMAN TROPHOBLAST; FETAL-GROWTH;
D O I
10.3390/genes13050752
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
(1) Background: Glucose is transferred from maternal blood to the fetus by glucose transporters. What is the effect of hypoxia on the gene expression of placenta glucose transporter 1 (GLUT1) and glucose transporter 3 (GLUT3) in growth-restricted fetus is interesting. (2) Methods: The gene expression of GLUT1 and GLUT3 and the protein expression of HIF-1 alpha were evaluated under nonhypoxic conditions and after 4 and 8 h under hypoxic conditions in placental mesenchymal stem cells derived from monochorionic twin pregnancies with selective intrauterine growth restriction. (3) Results: The gene expressions of GLUT1 and GLUT3 under hypoxia conditions were higher in placental mesenchymal stem cells derived from appropriate-for-gestational-age fetuses than in those from selective intrauterine growth-restricted fetuses. However, the protein expression of hypoxia induced factor-1 alpha (HIF-1 alpha) at hypoxia condition was not lower in placenta mesenchymal stem cells from selective intrauterine growth-restricted fetuses than in placental mesenchymal stem cells from appropriate-for-gestational-age fetuses. (4) Conclusions: Hypoxia-induced upregulation of GLUT1 and GLUT3 expression was decreased in placental mesenchymal stem cells from selective intrauterine growth-restricted fetuses but not due to decreased HIF-1 alpha expression. Selective growth-restricted fetuses have less capacity for hypoxia-induced upregulation of placental glucose transport.
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页数:9
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