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电压门控钙通道为神经元细胞培养物中铁的摄取提供了一条替代途径。

Voltage-gated calcium channels provide an alternate route for iron uptake in neuronal cell cultures.

作者信息

Gaasch Julie A, Geldenhuys Werner J, Lockman Paul R, Allen David D, Van der Schyf Cornelis J

机构信息

Department of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, School of Pharmacy, Amarillo, Texas 79106, USA.

出版信息

Neurochem Res. 2007 Oct;32(10):1686-93. doi: 10.1007/s11064-007-9313-1. Epub 2007 Apr 3.

Abstract

Recent studies suggest that iron enters cardiomyocytes via the L-type voltage-gated calcium channel (VGCC). The neuronal VGCC may also provide iron entry. As with calcium, extraneous iron is associated with the pathology and progression of neurodegenerative diseases such as Parkinson's and Alzheimer's disease. VGCCs, ubiquitously expressed, may be an important route of excessive entry for both iron and calcium, contributing to cell toxicity or death. We evaluated the uptake of (45)Ca(2+) and (55)Fe(2+) into NGF-treated rat PC12, and murine N-2alpha cells. Iron not only competed with calcium for entry into these cells, but iron uptake (similar to calcium uptake) was inhibited by nimodipine, a specific L-type VGCC blocker, and enhanced by FPL 64176, an L-VGCC activator, in a dose-dependent manner. Taken together, these data suggest that voltage-gated calcium channels are an alternate route for iron entry into neuronal cells under conditions that promote cellular iron overload toxicity.

摘要

近期研究表明,铁通过L型电压门控钙通道(VGCC)进入心肌细胞。神经元VGCC也可能为铁的进入提供途径。与钙一样,外源性铁与帕金森病和阿尔茨海默病等神经退行性疾病的病理和进展相关。广泛表达的VGCC可能是铁和钙过度进入的重要途径,导致细胞毒性或死亡。我们评估了(45)Ca(2+)和(55)Fe(2+)在经神经生长因子(NGF)处理的大鼠嗜铬细胞瘤(PC12)细胞和小鼠N-2α细胞中的摄取情况。铁不仅与钙竞争进入这些细胞,而且铁摄取(类似于钙摄取)受到特异性L型VGCC阻滞剂尼莫地平的抑制,并被L型VGCC激活剂FPL 64176以剂量依赖性方式增强。综上所述,这些数据表明,在促进细胞铁过载毒性的条件下,电压门控钙通道是铁进入神经元细胞的另一条途径。

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