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正常妊娠和子痫前期妇女胎盘动脉中 KCNQ 钾通道的表达和功能。

The expression and function of KCNQ potassium channels in human chorionic plate arteries from women with normal pregnancies and pre-eclampsia.

机构信息

Department of Gynecology and Obstetrics, the Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.

Key Laboratory of Medical Electrophysiology of Ministry of Education, Collaborative Innovation Center for Prevention and Treatment of Cardiovascular Research, Southwest Medical University, Luzhou, Sichuan, China.

出版信息

PLoS One. 2018 Mar 26;13(3):e0192122. doi: 10.1371/journal.pone.0192122. eCollection 2018.

Abstract

Pre-eclampsia is associated with altered maternal and placental vascular reactivity. Kv7 channels (encoded by KCNQ 1-5 genes) are a potential contributor to the regulation of vascular tone in CPAs (chorionic plate arteries) during normal pregnancy. The aim of this study is to establish the expression profile of KCNQ subunits in CPAs taken from women with preeclampsia or normotensive women and to examine the functional relevance of the Kv7 channels on an altered expression profile of KCNQ subunits. The effects of Kv7 channel modulators on CPAs were investigated by tension measurement. Quantitative PCR experiments were used to analyze the expression of KCNQ genes. Western blotting and immunofluorescence were both used to analyze the protein expression of Kv7 channels. Finally, in CPAs from normotensive women, the Kv7 channel blocker XE991 increased arterial basal tone and U46619-induced contraction, and pre-contracted CPAs (10-7 M U46619) exhibited significant relaxation following treatment with Retigabine(Kv7.2-7.5 activator) and BMS-204352(Kv7.2-7.5 activator). However, ICA-27243(selective KCNQ2 and KCNQ3 activator) and ML277(selective KV7.1 activator) had no significant effect on tension in the pre-contracted CPAs. Conversely, compared with CPAs from normotensive women, the effects of XE991 on basal tone and agonist (U46619)-induced contractions in CPAs from women with preeclampsia were markedly attenuated. Moreover, the relaxation effects of Retigabine and BMS-204352 on pre-contracted CPA vessels from women with pre-eclampsia were also markedly down-regulated. Interestingly, the relaxation ability of ICA-27243 in pre-contracted CPA vessels in women with pre-eclampsia was enhanced. The mRNA of KCNQ3 was specifically up-regulated, whereas those for KCNQ4 and KCNQ5 were down-regulated in CPAs from women with pre-eclampsia compared with those in normotensive women. Similar observations were found in a subsequent analysis of protein expression of KCNQ genes 3-5. Thus, down-regulated Kv7 channel function in tension regulation of CPAs in women with pre-eclampsia could be associated with considerably altered expression profiles of Kv7 subunits.

摘要

子痫前期与母体和胎盘血管反应性改变有关。Kv7 通道(由 KCNQ1-5 基因编码)可能是正常妊娠期间 CPAs(绒毛板血管)血管张力调节的一个潜在贡献者。本研究的目的是建立子痫前期妇女和正常血压妇女 CPAs 中 KCNQ 亚单位表达谱,并研究 Kv7 通道在改变的 KCNQ 亚单位表达谱中的功能相关性。通过张力测量研究 Kv7 通道调节剂对 CPAs 的影响。定量 PCR 实验用于分析 KCNQ 基因的表达。Western blot 和免疫荧光均用于分析 Kv7 通道的蛋白表达。最后,在正常血压妇女的 CPAs 中,Kv7 通道阻滞剂 XE991 增加了动脉基础张力和 U46619 诱导的收缩,并且预收缩的 CPAs(10-7 M U46619)在用 Retigabine(Kv7.2-7.5 激活剂)和 BMS-204352(Kv7.2-7.5 激活剂)处理后表现出显著的松弛。然而,ICA-27243(选择性 KCNQ2 和 KCNQ3 激活剂)和 ML277(选择性 Kv7.1 激活剂)对预收缩 CPAs 的张力没有显著影响。相反,与正常血压妇女的 CPAs 相比,XE991 对 CPAs 基础张力和激动剂(U46619)诱导收缩的作用在子痫前期妇女的 CPAs 中明显减弱。此外,Retigabine 和 BMS-204352 对预收缩 CPAs 血管的松弛作用在子痫前期妇女中也明显下调。有趣的是,ICA-27243 在子痫前期妇女预收缩 CPAs 中的松弛能力增强。与正常血压妇女相比,子痫前期妇女的 CPAs 中 KCNQ3 的 mRNA 特异性上调,而 KCNQ4 和 KCNQ5 的 mRNA 下调。在随后对 KCNQ 基因 3-5 蛋白表达的分析中也观察到了类似的结果。因此,子痫前期妇女 CPAs 张力调节中 Kv7 通道功能下调可能与 Kv7 亚单位表达谱的显著改变有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3814/5868761/2e58a998e8db/pone.0192122.g001.jpg

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