From the Departments of Anesthesia (E.C., Y.L., L.S., P.E.H.).
Medicine (S.D., E.L., T.A.L., S.A.K.).
Hypertension. 2018 Jul;72(1):219-226. doi: 10.1161/HYPERTENSIONAHA.118.11153. Epub 2018 May 29.
The molecular mechanisms underlying seizure susceptibility in preeclampsia are unknown. We hypothesized that altered expression of distinct proteins in the cerebrospinal fluid (CSF) may reflect pathophysiological changes in the central nervous system that contribute to the neurological manifestations of severe preeclampsia. We obtained CSF samples from 13 patients with preeclampsia and 14 control patients during spinal anesthesia before delivery and analyzed them by SOMAscan, an aptamer-based proteomics platform for alterations in 1310 protein levels. Ingenuity Pathway Analysis was conducted to highlight relationships between preeclampsia-specific proteins found to be significantly altered. For 2 of the target proteins, we validated the difference in CSF concentrations by ELISA. SOMAscan revealed 82 proteins, whose expression levels were significantly different (<0.05) in CSF from patients with preeclampsia versus controls. Principal component analysis achieved perfect separation of the preeclampsia and control groups in 2 dimensions. The differentially expressed proteins converge around 4 signaling molecules: TGF-β (transforming growth factor-β), VEGFA (vascular endothelial growth factor A), angiotensinogen, and IL-6 (interleukin-6). Within the TGF-β pathway, upregulation of activin A (301.6±47.4 versus 151.6±20.5 pg/mL; =0.0074) and follistatin-related gene (5129±347 versus 3016±188 pg/mL; <0.0001) in preeclampsia was confirmed by ELISA. In summary, signaling pathways important for vascular remodeling, inflammation, and neuronal growth, signaling, and electrophysiology were well represented among the proteins found to be altered in CSF in patients with preeclampsia.
子痫前期患者癫痫易感性的分子机制尚不清楚。我们假设脑脊液(CSF)中不同蛋白质表达的改变可能反映了中枢神经系统的病理生理变化,这些变化导致了严重子痫前期的神经表现。我们在分娩前脊髓麻醉期间从 13 例子痫前期患者和 14 例对照患者中获得 CSF 样本,并通过 SOMAscan 进行分析,SOMAscan 是一种基于适体的蛋白质组学平台,用于分析 1310 种蛋白质水平的变化。进行了 Ingenuity 通路分析,以突出发现的与子痫前期特异性蛋白显著改变相关的关系。对于 2 个目标蛋白,我们通过 ELISA 验证了 CSF 浓度的差异。SOMAscan 显示,82 种蛋白质的表达水平在子痫前期患者与对照组的 CSF 中存在显著差异(<0.05)。主成分分析在 2 个维度上实现了子痫前期和对照组的完美分离。差异表达的蛋白质集中在 4 个信号分子周围:TGF-β(转化生长因子-β)、VEGFA(血管内皮生长因子 A)、血管紧张素原和 IL-6(白细胞介素-6)。在 TGF-β 通路中,通过 ELISA 证实了激活素 A(301.6±47.4 与 151.6±20.5 pg/mL;=0.0074)和卵泡抑素相关基因(5129±347 与 3016±188 pg/mL;<0.0001)在子痫前期中的上调。总之,在子痫前期患者 CSF 中改变的蛋白质中,重要的血管重塑、炎症和神经元生长、信号转导和电生理学信号通路得到了很好的体现。