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

机译:对细胞质[Ca2 +]的单细胞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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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[Ca2 +]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。在这项研究中,我们对单个PC12细胞和人类神经元中的胞质[Ca2 +]的变化进行了全面研究,该变化是通过连续暴露于含有Aβ42的培养基中数天而引起的。 Aβ42诱导的[Ca2 +]增加的不同时机和幅度揭示了对Aβ42具有不同敏感性的细胞亚群。这些结果表明,Aβ产生的对胞质[Ca2 +]水平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Zn2 +和小肽NA7)获得的结果进一步证明了以下提示:持续暴露于Aβ应激的细胞中胞质[Ca2 +]的长期增加是由于Aβ离子通道活性。

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