首页> 外文期刊>Molecular pharmacology. >Sustained activation of N-methyl-D-aspartate receptors in podoctyes leads to oxidative stress, mobilization of transient receptor potential canonical 6 channels, nuclear factor of activated T cells activation, and apoptotic cell death
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Sustained activation of N-methyl-D-aspartate receptors in podoctyes leads to oxidative stress, mobilization of transient receptor potential canonical 6 channels, nuclear factor of activated T cells activation, and apoptotic cell death

机译:荚果中N-甲基-D-天冬氨酸受体的持续活化导致氧化应激,瞬时受体电位经典6通道动员,活化T细胞活化的核因子和凋亡细胞死亡

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Atypical N-methyl-D-aspartate (NMDA) receptors are expressed in podocytes. Sustained (≥24 h) application of 50 to 100 μM NMDA to immortalized mouse podocytes evoked a marked increase in the production of reactive oxygen species (ROS) such as H2O2. This effect of NMDA was associated with increased cell-surface expression of p47(phox), a cytosolic regulatory subunit of the NADPH oxidase NOX2. NMDA-evoked generation of ROS drove an increase in steady-state surface expression of transient receptor potential canonical (TRPC) 6 channels, which was blocked by the NMDA antagonist dizocilpine (MK-801) and by a membrane-permeable scavenger of ROS. The effect of NMDA on TRPC6 was observed using cell surface biotinylation assays and also with whole-cell recordings made under conditions designed to facilitate detection of current through TRPC6. NMDA mobilization of TRPC6 channels was blocked by concurrent treatment with the NMDA antagonist MK-801 and by a membrane-permeable scavenger of ROS. Mobilization of TRPC6 was also evoked by L-homocysteic acid. NMDA treatment also increased nuclear localization of endogenous nuclear factor of activated T cells, which could be blocked by MK-801, by scavenging ROS, by the calcineurin inhibitor cyclosporine, and by the TRPC channel inhibitor 1-[2-(4-methoxyphenyl)-2-[3-(4-methoxyphenyl)propoxy] ethyl]imidazole (SKF-96365). NMDA treatment also evoked robust activation of Rho but not Rac, consistent with previous studies of downstream effectors of TRPC6 activation. Exposing cells to NMDA for 24 h reduced total and cell surface expression of the podocyte markers nephrin and podocin, but there was no loss of cells. With longer NMDA exposure (72 h), we observed loss of cells associated with nuclear fragmentation and increased expression of caspase-3, caspase-6, and Bax, suggesting an apoptotic process.
机译:非典型的N-甲基-D-天冬氨酸(NMDA)受体在足细胞中表达。将50到100μMNMDA持续(≥24 h)施加到永生的小鼠足细胞上会引起活性氧(ROS)(例如H2O2)的产生显着增加。 NMDA的这种作用与p47(phox)(NADPH氧化酶NOX2的胞质调节亚基)的细胞表面表达增加有关。 NMDA诱发的ROS的产生推动了瞬时受体电位经典(TRPC)6通道的稳态表面表达的增加,这被NMDA拮抗剂二唑西平(MK-801)和膜透性的ROS清除剂阻断。使用细胞表面生物素化测定法以及在旨在促进通过TRPC6的电流检测的条件下进行的全细胞记录,可以观察到NMDA对TRPC6的影响。 TRPC6通道的NMDA动员被NMDA拮抗剂MK-801同时治疗和膜透性ROS清除所阻止。 L-同型半胱氨酸还引起了TRPC6的动员。 NMDA处理还增加了活化T细胞的内源性核因子的核定位,这可能被MK-801,清除ROS,钙调神经磷酸酶抑制剂环孢菌素和TRPC通道抑制剂1- [2-(4-甲氧基苯基)阻断-2- [3-(4-甲氧基苯基)丙氧基]乙基]咪唑(SKF-96365)。 NMDA处理还引起了Rho的强活化,但并未引起Rac的活化,这与先前对TRPC6活化下游效应子的研究一致。将细胞暴露于NMDA中24小时会降低足细胞标记物nephrin和podocin的总表达和细胞表面表达,但没有细胞丢失。在更长的NMDA暴露时间(72小时)中,我们观察到与核碎裂相关的细胞丢失以及caspase-3,caspase-6和Bax表达的增加,提示其凋亡过程。

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