George Eric M, Garrett Michael R, Granger Joey P
Departments of Physiology and Biophysics, University of Mississippi Medical Center, 2500 N. State St., Jackson, MS, 39216, USA,
Mamm Genome. 2014 Jun;25(5-6):253-61. doi: 10.1007/s00335-014-9505-3. Epub 2014 Mar 26.
Preeclampsia is a serious and common hypertensive complication of pregnancy, affecting ~5 to 8 % of pregnancies. The underlying cause of preeclampsia is believed to be placental ischemia, which causes secretion of pathogenic factors into the maternal circulation. While a number of these factors have been identified, it is likely that others remain to be elucidated. Here, we have utilized a relevant preclinical rodent model of placental ischemia-induced hypertension, the reduced uterine perfusion pressure (RUPP) model, to determine the effect of chronic placental ischemia on the underlying chorionic tissue and placental villi. Tissue from control and RUPP rats were isolated on gestational day 19 and mRNA from these tissues was subjected to microarray analysis to determine differential gene expression. At a statistical cutoff of p < 0.05, some 2,557 genes were differentially regulated between the two groups. Interestingly, only a small subset (22) of these genes exhibited changes of greater than 50 % versus control, a large proportion of which were subsequently confirmed using qRT-PCR analysis. Network analysis indicated a strong effect on inflammatory pathways, including those involving NF-κB and inflammatory cytokines. Of the most differentially expressed genes, the predominant gene classes were extracellular remodeling proteins, pro-inflammatory proteins, and a coordinated upregulation of the prolactin genes. The functional implications of these novel factors are discussed.
子痫前期是一种严重且常见的妊娠高血压并发症,影响约5%至8%的妊娠。子痫前期的潜在病因被认为是胎盘缺血,这会导致致病因子分泌到母体循环中。虽然已经确定了许多此类因子,但可能还有其他因子有待阐明。在此,我们利用了一种相关的胎盘缺血诱导高血压的临床前啮齿动物模型——降低子宫灌注压(RUPP)模型,来确定慢性胎盘缺血对潜在绒毛膜组织和胎盘绒毛的影响。在妊娠第19天分离对照大鼠和RUPP大鼠的组织,并对这些组织的mRNA进行微阵列分析以确定差异基因表达。在统计学临界值p < 0.05时,两组之间约有2557个基因受到差异调节。有趣的是,这些基因中只有一小部分(22个)与对照相比表现出大于50%的变化,其中很大一部分随后通过qRT-PCR分析得到证实。网络分析表明对炎症途径有强烈影响,包括涉及NF-κB和炎症细胞因子的途径。在差异表达最显著的基因中,主要的基因类别是细胞外重塑蛋白、促炎蛋白以及催乳素基因的协同上调。讨论了这些新因子的功能意义。