Guo Q, Sebastian L, Sopher B L, Miller M W, Ware C B, Martin G M, Mattson M P
Sanders-Brown Research Center on Aging and Department of Anatomy and Neurobiology, University of Kentucky, Lexington 40536-0230, USA.
J Neurochem. 1999 Mar;72(3):1019-29. doi: 10.1046/j.1471-4159.1999.0721019.x.
Many cases of early-onset inherited Alzheimer's disease (AD) are caused by mutations in the presenilin-1 (PS1) gene. Overexpression of PS1 mutations in cultured PC12 cells increases their vulnerability to apoptosis-induced trophic factor withdrawal and oxidative insults. We now report that primary hippocampal neurons from PS1 mutant knock-in mice, which express the human PS1M146V mutation at normal levels, exhibit increased vulnerability to amyloid beta-peptide toxicity. The endangering action of mutant PS1 was associated with increased superoxide production, mitochondrial membrane depolarization, and caspase activation. The peroxynitrite-scavenging antioxidant uric acid and the caspase inhibitor benzyloxycarbonyl-Val-Ala-Asp-fluoromethyl ketone protected hippocampal neurons expressing mutant PS1 against cell death induced by amyloid beta-peptide. Increased oxidative stress may contribute to the pathogenic action of PS1 mutations, and antioxidants may counteract the adverse property of such AD-linked mutations.
许多早发性遗传性阿尔茨海默病(AD)病例是由早老素-1(PS1)基因突变引起的。在培养的PC12细胞中PS1突变的过表达增加了它们对凋亡诱导的营养因子撤除和氧化损伤的易感性。我们现在报告,来自PS1突变基因敲入小鼠的原代海马神经元,其以正常水平表达人PS1M146V突变,对淀粉样β肽毒性表现出增加的易感性。突变型PS1的危害作用与超氧化物产生增加、线粒体膜去极化和半胱天冬酶激活有关。过氧亚硝酸盐清除抗氧化剂尿酸和半胱天冬酶抑制剂苄氧羰基-Val-Ala-Asp-氟甲基酮保护表达突变型PS1的海马神经元免受淀粉样β肽诱导的细胞死亡。氧化应激增加可能有助于PS1突变的致病作用,而抗氧化剂可能抵消此类与AD相关突变的不良特性。