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对胞质[Ca(2+)]进行单细胞筛选揭示了阿尔茨海默病Aβ肽离子通道的细胞选择性作用。

Single-cell screening of cytosolic [Ca(2+)] reveals cell-selective action by the Alzheimer's Aβ peptide ion channel.

作者信息

Lin Hopi, Arispe Nelson J

机构信息

Department of Anatomy, Physiology and Genetics, and Institute for Molecular Medicine, Uniformed Services University School of Medicine, USUHS, Bethesda, MD, 20814, USA.

出版信息

Cell Stress Chaperones. 2015 Mar;20(2):333-42. doi: 10.1007/s12192-014-0551-2. Epub 2014 Nov 1.

Abstract

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.

摘要

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。

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本文引用的文献

1
Multivariate analyses of amyloid-beta oligomer populations indicate a connection between pore formation and cytotoxicity.
PLoS One. 2012;7(10):e47261. doi: 10.1371/journal.pone.0047261. Epub 2012 Oct 15.
2
Two-step mechanism of membrane disruption by Aβ through membrane fragmentation and pore formation.
Biophys J. 2012 Aug 22;103(4):702-10. doi: 10.1016/j.bpj.2012.06.045.
3
Alzheimer Aβ peptide interactions with lipid membranes: fibrils, oligomers and polymorphic amyloid channels.
Prion. 2012 Sep-Oct;6(4):339-45. doi: 10.4161/pri.21022. Epub 2012 Aug 9.
4
Shear forces during blast, not abrupt changes in pressure alone, generate calcium activity in human brain cells.
PLoS One. 2012;7(6):e39421. doi: 10.1371/journal.pone.0039421. Epub 2012 Jun 29.
5
Calcium signaling and neurodegeneration.
Acta Naturae. 2010 Apr;2(1):72-82.
6
Single-channel Ca(2+) imaging implicates Aβ1-42 amyloid pores in Alzheimer's disease pathology.
J Cell Biol. 2011 Oct 31;195(3):515-24. doi: 10.1083/jcb.201104133. Epub 2011 Oct 24.
10
Synaptotoxicity of Alzheimer beta amyloid can be explained by its membrane perforating property.
PLoS One. 2010 Jul 27;5(7):e11820. doi: 10.1371/journal.pone.0011820.

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