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母体营养不良的胎儿肾脏表现出肾发生基因的差异调节,包括 Notch 信号通路的下调。

Maternal undernourished fetal kidneys exhibit differential regulation of nephrogenic genes including downregulation of the Notch signaling pathway.

机构信息

Department of Obstetrics and Gynecology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.

出版信息

Reprod Sci. 2011 Jun;18(6):563-76. doi: 10.1177/1933719110393025. Epub 2011 Jan 27.

Abstract

Maternal undernutrition results in offspring nephron number reduction and hypertension that are hypothesized to begin as compensatory changes in fetal gene expression during gestation. To evaluate mechanisms of dysregulated nephrogenesis, pregnant Sprague Dawley rats were 50% food restricted from embryonic day (E) 10 to E20. At E20, fetal male kidneys were examined by microarray analysis. A total of 476 differentially expressed transcripts were detected including those regulating development and differentiation, mitosis and cell cycle, chromatin assembly, and steroid hormone regulation. Differentially regulated genes were detected in MAPK/ERK, Wnt, and Notch signaling pathways. Validation of the microarray results was performed for the Notch signaling pathway, an important pathway in nephron formation. Protein expression of Notch pathway factors by Western blotting showed significantly decreased Notch2 and downstream effector Hey1 protein expression, while Ctbp1 co-repressor was increased. These data together show that maternal undernutrition results in developmental disruption in fetal nephrogenesis gene expression signaling.

摘要

母体营养不足导致后代肾单位数量减少和高血压,据推测,这些变化始于妊娠期间胎儿基因表达的代偿性改变。为了评估发育失调的肾发生机制,将妊娠 Sprague Dawley 大鼠从胚胎第 10 天(E)到第 20 天(E)进行 50%的食物限制。在 E20 时,通过微阵列分析检查胎儿雄性肾脏。共检测到 476 个差异表达的转录本,包括调节发育和分化、有丝分裂和细胞周期、染色质组装和甾体激素调节的转录本。在 MAPK/ERK、Wnt 和 Notch 信号通路中检测到差异调节的基因。对 Notch 信号通路进行了微阵列结果的验证,该通路是肾单位形成的重要通路。Western 印迹法显示 Notch 信号通路因子的蛋白表达显著降低 Notch2 和下游效应因子 Hey1 的蛋白表达,而 Ctbp1 共抑制因子增加。这些数据共同表明,母体营养不足导致胎儿肾发生基因表达信号的发育中断。

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