Suppr超能文献

早老素-1突变小鼠皮质突触区室中钙稳态改变与线粒体功能障碍

Altered calcium homeostasis and mitochondrial dysfunction in cortical synaptic compartments of presenilin-1 mutant mice.

作者信息

Begley J G, Duan W, Chan S, Duff K, Mattson M P

机构信息

Sanders-Brown Research Center on Aging and Department of Anatomy and Neurobiology, University of Kentucky, Lexington 40536-0230, USA.

出版信息

J Neurochem. 1999 Mar;72(3):1030-9. doi: 10.1046/j.1471-4159.1999.0721030.x.

Abstract

Alzheimer's disease is characterized by amyloid beta-peptide deposition, synapse loss, and neuronal death, which are correlated with cognitive impairments. Mutations in the presenilin-1 gene on chromosome 14 are causally linked to many cases of early-onset inherited Alzheimer's disease. We report that synaptosomes prepared from transgenic mice harboring presenilin-1 mutations exhibit enhanced elevations of cytoplasmic calcium levels following exposure to depolarizing agents, amyloid beta-peptide, and a mitochondrial toxin compared with synaptosomes from nontransgenic mice and mice overexpressing wild-type presenilin-1. Mitochondrial dysfunction and caspase activation following exposures to amyloid beta-peptide and metabolic insults were exacerbated in synaptosomes from presenilin-1 mutant mice. Agents that buffer cytoplasmic calcium or that prevent calcium release from the endoplasmic reticulum protected synaptosomes against the adverse effect of presenilin-1 mutations on mitochondrial function. Abnormal synaptic calcium homeostasis and mitochondrial dysfunction may contribute to the pathogenic mechanism of presenilin-1 mutations.

摘要

阿尔茨海默病的特征是β-淀粉样肽沉积、突触丧失和神经元死亡,这些都与认知障碍相关。14号染色体上早老素-1基因的突变与许多早发性遗传性阿尔茨海默病病例存在因果联系。我们报告称,与来自非转基因小鼠和过表达野生型早老素-1的小鼠的突触体相比,从携带早老素-1突变的转基因小鼠制备的突触体在暴露于去极化剂、β-淀粉样肽和线粒体毒素后,细胞质钙水平升高更为明显。早老素-1突变小鼠的突触体在暴露于β-淀粉样肽和代谢损伤后,线粒体功能障碍和半胱天冬酶激活加剧。缓冲细胞质钙或阻止钙从内质网释放的试剂可保护突触体免受早老素-1突变对线粒体功能的不利影响。异常的突触钙稳态和线粒体功能障碍可能有助于早老素-1突变的致病机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验