Lin Hopi, Arispe Nelson J
Department of Anatomy, Physiology and Genetics, and Institute for Molecular Medicine, Uniformed Services University School of Medicine, USUHS, Bethesda, MD, 20814, USA.
Cell Stress Chaperones. 2015 Mar;20(2):333-42. doi: 10.1007/s12192-014-0551-2. Epub 2014 Nov 1.
Interaction of the Alzheimer's Aβ peptides with the plasma membrane of cells in culture results in chronic increases in cytosolic [Ca(2+)]. 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 [Ca(2+)] 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 [Ca(2+)] reveal subpopulations of cells with differential sensitivity to Aβ42. These results suggest that the effect produced by Aβ on the level of cytosolic [Ca(2+)] depends on the type of cell being monitored. Moreover, the results obtained of using potent inhibitors of Aβ cation channels such as Zn(2+) and the small peptide NA7 add further proof to the suggestion that the long-term increases in cytosolic [Ca(2+)] in cells stressed by continuous exposure to Aβ is the result of Aβ ion channel activity.
阿尔茨海默病的Aβ肽与培养细胞的质膜相互作用会导致胞质[Ca(2+)]持续增加。这种增加会引起多种继发效应,导致细胞生长受损或细胞变性。在本研究中,我们全面研究了连续数天暴露于含Aβ42培养基中的单个PC12细胞和人类神经元中胞质[Ca(2+)]的变化。Aβ42诱导的[Ca(2+)]增加的不同时间和幅度揭示了对Aβ42敏感性不同的细胞亚群。这些结果表明,Aβ对胞质[Ca(2+)]水平的影响取决于所监测的细胞类型。此外,使用Aβ阳离子通道强效抑制剂(如Zn(2+)和小肽NA7)所获得的结果进一步证明,连续暴露于Aβ的应激细胞中胞质[Ca(2+)]的长期增加是Aβ离子通道活性的结果。