A New Perspective of Lysosomal Cation Channel-Dependent Homeostasis in Alzheimer's Disease
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- 作者：Martin Ezeani ; Maxwell Omabe
- 关键词：Lysosomal Cation Channels ; Cation homeostasis ; AD ; PHL
- 刊名：Molecular Neurobiology
- 出版年：2016
- 出版时间：April 2016
- 年：2016
- 卷：53
- 期：3
- 页码：1672-1678
- 全文大小：691 KB
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Maxwell Omabe (2)
1. Department of Physiology and Biophysics, Faculty of Medicine, Dalhousie University, Sir Charles Tupper Medical Building, 5850 College Street, Halifax, B3H 4R2, Nova Scotia, Canada
2. Cancer Research Unit, Saskatchewan Cancer Agency, Department of Oncology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada - 刊物主题：Neurosciences; Neurobiology; Cell Biology; Neurology;
- 出版者：Springer US
- ISSN：1559-1182
文摘
Studies have reported typically biophysical lysosomal cation channels including TPCs. Their plausible biological roles are being elucidated by pharmacological, genetic and conventional patch clamp procedures. The best characterized so far among these channels is the ML1 isoform of TRP. The reported TRPs and TPCs are bypass for cation fluxes and are strategic for homeostasis of ionic milieu of the acidic organelles they confine to. Ca2+ homeostasis and adequate acidic pHL are critically influential for the regulation of a plethora of biological functions these intracellular cation channels perform. In lysosomal ion channel biology, we review: ML1 and TPC2 in Ca2+ signaling, ML1 and TPC2 in pHL regulation. Using Aβ42 and tau proteins found along clathrin endolysosomal internalization pathway (Fig. 3), we proffer a mechanism of abnormal pHL and ML1/TPC2-dependent cation homeostasis in AD.