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Single-cell screening of cytosolic Ca2+ reveals cell-selective action by the Alzheimer’s Aβ peptide ion channel

机译:单细胞胞浆Ca2 +的筛选揭示了阿尔茨海默氏症Aβ肽离子通道的细胞选择性作用

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摘要

Interaction of the Alzheimer’s Aβ peptides with the plasma membrane of cells in culture results in chronic increases in cytosolic [Ca2+]. Such increases can cause a variety of secondary effects leading to impaired cell growth or cell degeneration. In this investigation, we made a comprehensive study of the changes in cytosolic [Ca2+] in single PC12 cells and human neurons stressed by continuous exposure to a medium containing Aβ42 for several days. The differential timing and magnitude of the Aβ42-induced increase in [Ca2+] reveal subpopulations of cells with differential sensitivity to Aβ42. These results suggest that the effect produced by Aβ on the level of cytosolic [Ca2+] depends on the type of cell being monitored. Moreover, the results obtained of using potent inhibitors of Aβ cation channels such as Zn2+ and the small peptide NA7 add further proof to the suggestion that the long-term increases in cytosolic [Ca2+] in cells stressed by continuous exposure to Aβ is the result of Aβ ion channel activity.
机译:阿尔茨海默氏症Aβ肽与培养细胞质膜的相互作用导致胞质[Ca 2 + ]的长期增加。这样的增加会引起多种次级效应,导致细胞生长受损或细胞变性。在这项调查中,我们对连续暴露于含有Aβ42的培养基中数天而承受压力的单个PC12细胞和人神经元中胞质[Ca 2 + ]的变化进行了全面研究。 Aβ42诱导的[Ca 2 + ]增加的时间和幅度的差异揭示了对Aβ42具有不同敏感性的细胞亚群。这些结果表明,Aβ对胞质[Ca 2 + ]水平产生的影响取决于所监测细胞的类型。此外,使用有效的Aβ阳离子通道抑制剂(如Zn 2 + 和小肽NA7)获得的结果进一步证明了胞质[Ca 2不断暴露于Aβ的细胞中的+ ]是Aβ离子通道活性的结果。

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