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活性氧抑制足月人合体滋养层细胞中的多囊蛋白-2(TRPP2)阳离子通道活性。

Reactive oxygen species inhibit polycystin-2 (TRPP2) cation channel activity in term human syncytiotrophoblast.

作者信息

Montalbetti N, Cantero M R, Dalghi M G, Cantiello H F

机构信息

Instituto de Investigaciones Cardiológicas UBA-CONICET, Buenos Aires, Argentina.

出版信息

Placenta. 2008 Jun;29(6):510-8. doi: 10.1016/j.placenta.2008.02.015. Epub 2008 Apr 15.

Abstract

Pregnancy is often associated with oxidative stress (OS) and lower antioxidant defences, which are both implicated in the pathophysiology of preeclampsia, free radical-induced birth defects, and abortions, as well as gestational diabetes mellitus (GDM), where products of lipid peroxidation are increased. The molecular target(s) of increased oxygen free radicals and consequent lipid peroxidation in the human placenta remains ill defined. The human syncytiotrophoblast (hST) expresses abundant polycystin-2 (PC2, TRPP2), a TRP-type Ca(2+)-permeable non-selective cation channel. Here, we explored the effect of reactive oxygen species (ROS) on PC2 channel activity of term hST. Apical membranes of the hST were reconstituted in a lipid bilayer chamber. Addition of either hydrogen-peroxide (H(2)O(2)) or tert-butyl hydroperoxide (tBHP) to the cis chamber (intracellular side) rapidly and completely inhibited PC2-mediated cation channel activity in reconstituted hST vesicles. A dose-response titration with increasing concentrations of H(2)O(2) gave an IC(50)=131 nM. The effect of H(2)O(2) on the isolated protein from in vitro transcribed/translated material was significantly different. H(2)O(2) inhibited PC2 cation channel activity, with a much lower affinity (IC(50)=193 microM). To correlate these findings with H(2)O(2)-induced lipid peroxidation, TBARS where measured in hST apical membranes incubated with H(2)O(2). Increased TBARS by exposure of hST apical membranes to H(2)O(2) (625 microM) returned to control value in the presence of catalase (167 microg/ml). Taken together these data indicate that ROS affect PC2 channel function by targetting both membrane lipids and the channel protein. Thus, OS in human pregnancy may be linked to dysregulation of channels such as PC2, which allow the transport of Ca(2+) into the placenta. Oxidative complications in pregnancy may implicate dysfunctional cation transfer between mother and fetus.

摘要

妊娠常与氧化应激(OS)及较低的抗氧化防御能力相关,这两者均与先兆子痫、自由基诱导的出生缺陷、流产以及妊娠期糖尿病(GDM)的病理生理学有关,在GDM中脂质过氧化产物会增加。人胎盘内氧自由基增加及随之发生的脂质过氧化的分子靶点仍不清楚。人合体滋养层细胞(hST)表达丰富的多囊蛋白-2(PC2,TRPP2),这是一种TRP型Ca(2+)通透性非选择性阳离子通道。在此,我们探究了活性氧(ROS)对足月hST的PC2通道活性的影响。hST的顶端膜在脂质双层小室中进行重组。向顺式小室(细胞内侧)添加过氧化氢(H(2)O(2))或叔丁基过氧化氢(tBHP)可迅速且完全抑制重组hST囊泡中PC2介导的阳离子通道活性。用浓度递增的H(2)O(2)进行剂量反应滴定得出IC(50)=131 nM。H(2)O(2)对体外转录/翻译材料中分离出的蛋白质的作用明显不同。H(2)O(2)抑制PC2阳离子通道活性,亲和力低得多(IC(50)=193 microM)。为了将这些发现与H(2)O(2)诱导的脂质过氧化相关联,在与H(2)O(2)孵育的hST顶端膜中测量了硫代巴比妥酸反应物(TBARS)。hST顶端膜暴露于H(2)O(2)(625 microM)后TBARS增加,在过氧化氢酶(167 microg/ml)存在的情况下恢复到对照值。综合这些数据表明,ROS通过靶向膜脂质和通道蛋白来影响PC2通道功能。因此,人类妊娠中的OS可能与诸如PC2等通道的失调有关,这些通道允许Ca(2+)转运至胎盘。妊娠中的氧化并发症可能意味着母婴之间阳离子转运功能失调。

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