First Department of Obstetrics and Gynecology, Semmelweis University, Budapest, Hungary.
Placenta. 2011 Feb;32 Suppl(0):S21-9. doi: 10.1016/j.placenta.2010.04.014. Epub 2010 Jun 11.
The involvement of the placenta in the pathogenesis of preeclampsia and HELLP syndrome is well established, and placental lesions are also similar in these two syndromes. Here we aimed to examine the placental transcriptome and to identify candidate biomarkers in early-onset preeclampsia and HELLP syndrome.
Placental specimens were obtained at C-sections from women with early-onset preeclampsia and HELLP syndrome, and from controls who delivered preterm or at term. After histopathological examination, fresh-frozen placental specimens were used for microarray profiling and validation by qRT-PCR. Differential expression was analysed using log-linear models while adjusting for gestational age. Gene ontology and pathway analyses were used to interpret gene expression changes. Tissue microarrays were constructed from paraffin-embedded placental specimens and immunostained.
Placental gene expression was gestational age-dependent among preterm and term controls. Out of the 350 differentially expressed genes in preeclampsia and 554 genes in HELLP syndrome, 224 genes (including LEP, CGB, LHB, INHA, SIGLEC6, PAPPA2, TREM1, and FLT1) changed in the same direction (elevated or reduced) in both syndromes. Many of these encode proteins that have been implicated as biomarkers for preeclampsia. Enrichment analyses revealed similar biological processes, cellular compartments and biological pathways enriched in early-onset preeclampsia and HELLP syndrome; however, some processes and pathways (e.g., cytokine-cytokine receptor interaction) were over-represented only in HELLP syndrome.
High-throughput transcriptional and tissue microarray expression profiling revealed that placental transcriptomes of early-onset preeclampsia and HELLP syndrome largely overlap, underlying a potential common cause and pathophysiologic processes in these syndromes. However, gene expression changes may also suggest a more severe placental pathology and pronounced inflammatory response in HELLP syndrome than in preeclampsia.
胎盘在子痫前期和 HELLP 综合征发病机制中的作用已得到充分证实,这两种综合征的胎盘病变也相似。在这里,我们旨在检查胎盘转录组,并确定早发型子痫前期和 HELLP 综合征的候选生物标志物。
在剖宫产时从早发型子痫前期和 HELLP 综合征患者以及早产或足月分娩的对照组中获取胎盘标本。在进行组织病理学检查后,使用新鲜冷冻胎盘标本进行微阵列分析,并通过 qRT-PCR 进行验证。使用对数线性模型分析差异表达,同时调整胎龄。使用基因本体论和途径分析来解释基因表达变化。从石蜡包埋的胎盘标本中构建组织微阵列并进行免疫染色。
在早产和足月对照组中,胎盘基因表达随胎龄而变化。在子痫前期的 350 个差异表达基因和 HELLP 综合征的 554 个基因中,224 个基因(包括 LEP、CGB、LHB、INHA、SIGLEC6、PAPPA2、TREM1 和 FLT1)在两种综合征中以相同的方向(升高或降低)变化。其中许多基因编码的蛋白质已被认为是子痫前期的生物标志物。富集分析显示,早发型子痫前期和 HELLP 综合征中存在相似的生物学过程、细胞区室和生物学途径;然而,一些过程和途径(例如细胞因子-细胞因子受体相互作用)仅在 HELLP 综合征中过度表达。
高通量转录组和组织微阵列表达谱分析表明,早发型子痫前期和 HELLP 综合征的胎盘转录组大部分重叠,这表明这些综合征存在潜在的共同病因和病理生理过程。然而,基因表达的变化也可能表明 HELLP 综合征中的胎盘病理更严重,炎症反应更明显。