APP转基因小鼠中β-淀粉样蛋白的蛋白水解增强可预防斑块形成、继发性病理变化和过早死亡。

Enhanced proteolysis of beta-amyloid in APP transgenic mice prevents plaque formation, secondary pathology, and premature death.

作者信息

Leissring Malcolm A, Farris Wesley, Chang Alice Y, Walsh Dominic M, Wu Xining, Sun Xiaoyan, Frosch Matthew P, Selkoe Dennis J

机构信息

Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Neuron. 2003 Dec 18;40(6):1087-93. doi: 10.1016/s0896-6273(03)00787-6.

Abstract

Converging evidence suggests that the accumulation of cerebral amyloid beta-protein (Abeta) in Alzheimer's disease (AD) reflects an imbalance between the production and degradation of this self-aggregating peptide. Upregulation of proteases that degrade Abeta thus represents a novel therapeutic approach to lowering steady-state Abeta levels, but the consequences of sustained upregulation in vivo have not been studied. Here we show that transgenic overexpression of insulin-degrading enzyme (IDE) or neprilysin (NEP) in neurons significantly reduces brain Abeta levels, retards or completely prevents amyloid plaque formation and its associated cytopathology, and rescues the premature lethality present in amyloid precursor protein (APP) transgenic mice. Our findings demonstrate that chronic upregulation of Abeta-degrading proteases represents an efficacious therapeutic approach to combating Alzheimer-type pathology in vivo.

摘要

越来越多的证据表明,阿尔茨海默病(AD)中脑淀粉样β蛋白(Aβ)的积累反映了这种自我聚集肽的产生与降解之间的失衡。因此,上调降解Aβ的蛋白酶代表了一种降低稳态Aβ水平的新型治疗方法,但体内持续上调的后果尚未得到研究。在此,我们表明,神经元中胰岛素降解酶(IDE)或中性内肽酶(NEP)的转基因过表达可显著降低脑内Aβ水平,延缓或完全阻止淀粉样斑块形成及其相关的细胞病理学变化,并挽救淀粉样前体蛋白(APP)转基因小鼠中出现的过早死亡。我们的研究结果表明,慢性上调Aβ降解蛋白酶是体内对抗阿尔茨海默型病理学的一种有效治疗方法。

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