The effect of oxygen tension on intracellular survival signalling in primary villous trophoblasts

被引:19
作者
Mackova, M
Kilani, RT
Davidge, ST
Guilbert, LJ
机构
[1] Univ Alberta, Dept Med Microbiol & Immunol, Perinatal Res Ctr, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Dept Obstet & Gynecol & Physiol, Perinatal Res Ctr, Edmonton, AB T6G 2S2, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1016/S0143-4004(03)00056-0
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Villous trophoblasts undergo increased apoptosis and experience a wider gradient of oxygen tensions (pO(2)) in pregnancies complicated by intrauterine growth restriction. We hypothesize that pO(2) affects trophoblast apoptosis by altering survival signalling through the phosphatidylinositol-3 (PI-3)-kinase and mitogen activated protein kinase (MAPK) pathways. Cytotrophoblasts were cultured at pO(2) from <10 to similar to140 mmHg with Epidermal Growth Factor (EGF), Vascular Endothelial Growth Factor (VEGF) and basic Fibroblast Growth Factor (bFGF) at concentrations of 0.1 to 10 ng/ml for 1 to 12 h, then assessed for apoptosis (TUNEL) and specific protein expressions (Western blot analysis). Spontaneous apoptosis was highest at <10 mmHg and lowest similar to15 mmHg. Only EGF activated either signalling pathway at any pO(2). Inhibition of both pathways was required to inhibit EGF-stimulated survival. Maximal EGF activation of either pathway was insensitive to pO(2). At lower oxygen tensions, MAPK phosphorylation was maximal at 1 ng/ml EGF compared with 10 ng/ml for the PI-3-kinase path. The EGF receptor was spontaneously phosphorylated with increasing culture times at lower oxygen levels, an effect reflected down-stream by PI-3-kinase and Akt phosphorylation. We conclude that strong survival signalling in trophoblasts requires both PI-3- and MAP-kinase pathways, is rather insensitive to pO(2) changes and is spontaneously activated with increasing hypoxic exposure. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:627 / 637
页数:11
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