Hsu Te-Yao, Lin Hao, Hung Hsuan-Ning, Yang Kuender D, Ou Chia-Yu, Tsai Ching-Chang, Cheng Hsin-Hsin, Chung Su-Hai, Cheng Bi-Hua, Wong Yi-Hsun, Chou An Kuo, Hsiao Chang-Chun
Department of Obstetrics and Gynecology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Chang Gung University College of Medicine, Kaohsiung, Taiwan.
PLoS One. 2016 Jan 11;11(1):e0145908. doi: 10.1371/journal.pone.0145908. eCollection 2016.
Edwards syndrome (ES) is a severe chromosomal abnormality with a prevalence of about 0.8 in 10,000 infants born alive. The aims of this study were to identify candidate proteins associated with ES pregnancies from amniotic fluid supernatant (AFS) using proteomics, and to explore the role of biological networks in the pathophysiology of ES.
AFS from six second trimester pregnancies with ES fetuses and six normal cases were included in this study. Fluorescence-based two-dimensional difference gel electrophoresis (2D-DIGE) and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/MS) were used for comparative proteomic analysis. The identified proteins were further validated by Western blotting and the role of biological networks was analyzed.
Twelve protein spots were differentially expressed by more than 1.5-fold in the AFS of the ES pregnancies. MALDI-TOF/MS identified one up-regulated protein: apolipoprotein A1 (ApoA1), and four under-regulated proteins: vitamin D binding protein (VDBP), alpha-1-antitrypsin (A1AT), insulin-like growth factor-binding protein 1 (IGFBP-1), and transthyretin (TTR). Western blot and densitometric analysis of ApoA1, A1AT, IGFBP-1, and TTR confirmed the alteration of these proteins in the amniotic fluid samples. Biological network analysis revealed that the proteins of the ES AFS were involved mainly in lipid and hormone metabolism, immune response, and cardiovascular disease.
These five proteins may be involved in the pathogenesis of ES. Further studies are needed to explore.
爱德华兹综合征(ES)是一种严重的染色体异常疾病,活产婴儿中的患病率约为万分之0.8。本研究的目的是利用蛋白质组学从羊水上清液(AFS)中鉴定与ES妊娠相关的候选蛋白质,并探讨生物网络在ES病理生理学中的作用。
本研究纳入了6例孕中期胎儿为ES的妊娠羊水样本和6例正常样本。采用基于荧光的二维差异凝胶电泳(2D-DIGE)和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF/MS)进行比较蛋白质组学分析。通过蛋白质免疫印迹法进一步验证鉴定出的蛋白质,并分析生物网络的作用。
在ES妊娠的AFS中,有12个蛋白点的差异表达倍数超过1.5倍。MALDI-TOF/MS鉴定出1种上调蛋白:载脂蛋白A1(ApoA1),以及4种下调蛋白:维生素D结合蛋白(VDBP)、α-1抗胰蛋白酶(A1AT)、胰岛素样生长因子结合蛋白1(IGFBP-1)和转甲状腺素蛋白(TTR)。对ApoA1、A1AT、IGFBP-1和TTR进行蛋白质免疫印迹和光密度分析,证实了这些蛋白质在羊水样本中的变化。生物网络分析显示,ES羊水样本中的蛋白质主要参与脂质和激素代谢、免疫反应及心血管疾病。
这5种蛋白质可能参与了ES的发病机制。需要进一步研究以进行探索。