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Proteome Differences of Placenta Between Pre-Eclampsia and Normal Pregnancy

期刊

PLACENTA
卷 31, 期 2, 页码 121-125

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W B SAUNDERS CO LTD
DOI: 10.1016/j.placenta.2009.11.004

关键词

Proteomics; Pre-eclampsia; Placenta; 2D-PAGE; Mass spectrometry

资金

  1. Shiraz University of Medical Sciences [88-4583]

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Placenta is a tissue unique to pregnancy and despite its major role in pregnancy. little is known about the proteome changes within placenta during pregnancy-related diseases such as pre-eclampsia (PE) Therefore, the ann of this study is the analysis of proteome differences between pre-eclamptic and normal full-term placentas To achieve this goal, five normal and five severe pre-eclamptic placentas were included in this study Total placental proteins were extracted and Subjected to two-dimensional polyacrylamide gel electrophoresis (2D-PAGE). After staining, the gels were scanned and the protein spots were analysed using Image Master 2D Platinum Software. Non-parametric Mann-Whitney test was used for analysis of the mean intensity differences of the spots between normal and pre-eclamptic placentas Statistical analysis indicated that 17 spots were differently expressed in pre-eclamptic compared with normal placentas (p < 0 05) Using Matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI TOF/TOF) mass analysis, 11 out of 17 spots were identified Among them, four proteins (chloride intracellular channel 3. apolipoprotein A-I, transthyretin (TTR) and protein disulphide isomerase) were up-regulated while seven (peroxiredoxin 2, peroxiredoxin 3, Hsc 70, Cu/Zn-superoxide dismutase (SOD-1), actin gamma 1 propeptide, chain A of enoyl-coenzyme A hydratase and HSP gp96) showed decreased expression in PE in comparison with normal placentas In conclusion, down-regulation of proteins with anti-oxidant activities (peroxiredoxin 2 and peroxiredoxin 3) and altered expression of stress-response proteins (Hsc 70, Hsp gp96 and protein disulphide isomerase) might play an important role in the pathogenesis of PE. (C) 2009 Elsevier Ltd All rights reserved

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