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胎盘组织块条件培养液代谢特征的变化可识别与缺氧和子痫前期相关的代谢紊乱。

Changes in the metabolic footprint of placental explant-conditioned culture medium identifies metabolic disturbances related to hypoxia and pre-eclampsia.

机构信息

Manchester Centre for Integrative Systems Biology, University of Manchester, M1 7DN, UK.

出版信息

Placenta. 2009 Nov;30(11):974-80. doi: 10.1016/j.placenta.2009.08.008. Epub 2009 Sep 22.

DOI:10.1016/j.placenta.2009.08.008
PMID:19775752
Abstract

Pre-eclampsia (PE) is a multi-system disorder thought to be mediated by circulating factors released from damaged placental villous trophoblast. There is extensive evidence of changes in the villous tissue in PE, some of which may be replicated by culturing villous tissue in hypoxic conditions. Metabolic footprinting offers a hypothesis-generating strategy to investigate factors released from this tissue in vitro. This study investigated differences in the factors released from villous trophoblast from uncomplicated pregnancies (n=6) and those with PE (n=6). In both cases, explanted placental villous fragments were cultured for 96 h in 1% O(2) (hypoxia) or 6% O(2) (placental normoxia). Metabolites consumed from and released into serum-conditioned culture medium were analysed by Ultra Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS). The relative concentration of 154 features of the metabolic footprint were observed to change in culture medium from uncomplicated pregnancies cultured in normoxic and hypoxic conditions (p<0.00005). 21 and 80 features were also different in culture medium from PE versus uncomplicated pregnancies cultured in hypoxic and normoxic conditions, respectively (p<0.00005). When comparing all 4 groups, 47 metabolic features showed a similar relative concentration in PE-derived media cultured in normoxic conditions to conditioned media from normal villous tissue cultured in hypoxic conditions. These data suggest that hypoxia may have a role in the placental pathogenesis of PE. Three areas of metabolism were highlighted for systems biology investigation; glutamate and glutamine, tryptophan metabolism and leukotriene or prostaglandin metabolism.

摘要

子痫前期(PE)被认为是一种多系统疾病,其发病机制与受损胎盘绒毛滋养层释放的循环因子有关。PE 绒毛组织存在广泛的变化,其中一些变化可以通过在低氧条件下培养绒毛组织来复制。代谢足迹提供了一种假设生成策略,可以在体外研究从该组织释放的因子。本研究比较了来自正常妊娠(n=6)和 PE(n=6)的绒毛滋养层释放的因子的差异。在这两种情况下,离体胎盘绒毛碎片在 1%O(2)(低氧)或 6%O(2)(胎盘正常氧)条件下培养 96 小时。通过超高效液相色谱-质谱联用仪(UPLC-MS)分析从血清条件培养基中消耗和释放的代谢物。观察到在正常氧和低氧条件下培养的正常妊娠培养物的培养基中,代谢足迹的 154 个特征的相对浓度发生变化(p<0.00005)。在低氧和正常氧条件下培养的 PE 与正常妊娠的培养基中,也有 21 个和 80 个特征不同(p<0.00005)。当比较所有 4 组时,47 种代谢特征在正常氧条件下培养的 PE 来源培养基中的相对浓度与低氧条件下培养的正常绒毛组织的条件培养基相似。这些数据表明,低氧可能在 PE 的胎盘发病机制中起作用。有三个代谢领域突出用于系统生物学研究;谷氨酸和谷氨酰胺、色氨酸代谢和白三烯或前列腺素代谢。

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