Barandalla M, Colleoni S, Lazzari G
Avantea srl, Laboratory of Reproductive Technologies, via Porcellasco 7/f, 26100 Cremona, Italy.
Cell Dev Biol. 2016 Aug;5(2). doi: 10.4172/2168-9296.1000177. Epub 2016 Aug 31.
Human Embryonic Stem Cells (hESCs) potentially offer a unique model to study how an adverse environment during the early developmental stages post-fertilization can affect the physiology of the undifferentiated embryonic stem cells existing in the early embryo and predispose to long term effects on the offspring, according to the Developmental Origins of Health and Disease (DOHaD) concept. A number of unfavourable conditions can affect the development of the early embryo inducing oxidative stress both , for instance in gestational diabetes and , when embryos are derived from Assisted Reproductive Technologies (ART). Therefore, the aim of this study was the development of a novel model to analyse the effects of oxidative stress and the antioxidant response against Reactive Oxygen Species (ROS) in embryonic stem cells in comparison with somatic cells, fibroblasts and endothelial cells. To this purpose we designed an protocol based on hydrogen peroxide (HO) treatment of 72 h, in order to better resemble the period of embryonic development from the early cleavages to the blastocyst stage. We demonstrate that HO treatment induces the modification of crucial oxidative stress biomarkers like ROS and lipid peroxidation levels, and mobilizes several antioxidant enzymes through NFkβ translocation. Moreover we show differences between somatic and embryonic cells in their antioxidant response towards HO induced damage. Therefore this study presents a promising model to investigate the effects of oxidative stress conditions on early human embryonic cells.
根据健康与疾病的发育起源(DOHaD)概念,人类胚胎干细胞(hESCs)可能提供一个独特的模型,用于研究受精后早期发育阶段的不利环境如何影响早期胚胎中未分化胚胎干细胞的生理功能,并对后代产生长期影响。许多不利条件会影响早期胚胎的发育,例如妊娠期糖尿病以及胚胎来自辅助生殖技术(ART)时,都会引发氧化应激。因此,本研究的目的是开发一种新型模型,以分析氧化应激的影响以及与体细胞、成纤维细胞和内皮细胞相比,胚胎干细胞对活性氧(ROS)的抗氧化反应。为此,我们设计了一个基于过氧化氢(HO)处理72小时的方案,以便更好地模拟从早期卵裂到囊胚阶段的胚胎发育时期。我们证明,HO处理会诱导关键氧化应激生物标志物如ROS和脂质过氧化水平的改变,并通过NFkβ易位调动几种抗氧化酶。此外,我们展示了体细胞和胚胎细胞在对HO诱导损伤的抗氧化反应方面的差异。因此,本研究提出了一个有前景的模型,用于研究氧化应激条件对早期人类胚胎细胞的影响。