The aged rhesus macaque manifests Braak stage III/IV Alzheimer's-like pathology

被引:95
作者
Paspalas, Constantinos D. [1 ]
Carlyle, Becky C. [2 ]
Leslie, Shannon [2 ]
Preuss, Todd M. [3 ]
Crimins, Johanna L. [1 ]
Huttner, Anita J. [4 ]
van Dyck, Christopher H. [1 ,2 ,5 ]
Rosene, Douglas L. [6 ]
Nairn, Angus C. [2 ]
Arnsten, Amy F. T. [1 ,2 ]
机构
[1] Yale Sch Med, Dept Neurosci, New Haven, CT 06510 USA
[2] Yale Sch Med, Dept Psychiat, New Haven, CT 06510 USA
[3] Emory Univ, Yerkes Natl Primate Ctr, Div Neuropharmacol & Neurol Dis, Atlanta, GA 30322 USA
[4] Yale Sch Med, Dept Pathol, New Haven, CT USA
[5] Yale Sch Med, Dept Neurol, New Haven, CT USA
[6] Boston Univ, Sch Med, Dept Anat & Neurobiol, Boston, MA 02118 USA
基金
美国国家卫生研究院;
关键词
Amyloid; Entorhinal cortex; Prefrontal cortex; Ryanodine receptor calcium leak; Tau phosphorylation; Animal model of disease; PAIRED HELICAL FILAMENTS; ENTORHINAL CORTEX; PRECURSOR PROTEIN; AMYLOID-BETA; COGNITIVE IMPAIRMENT; PKA PHOSPHORYLATION; PREFRONTAL CORTEX; A-BETA; DISEASE; TAU;
D O I
10.1016/j.jalz.2017.11.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: An animal model of late-onset Alzheimer's disease is needed to research what causes degeneration in the absence of dominant genetic insults and why the association cortex is particularly vulnerable to degeneration. Methods: We studied the progression of tau and amyloid cortical pathology in the aging rhesus macaque using immunoelectron microscopy and biochemical assays. Results: Aging macaques exhibited the same qualitative pattern and sequence of tau and amyloid cortical pathology as humans, reaching Braak stage III/IV. Pathology began in the young-adult entorhinal cortex with protein kinase A-phosphorylation of tau, progressing to fibrillation with paired helical filaments and mature tangles in oldest animals. Tau pathology in the dorsolateral prefrontal cortex paralleled but lagged behind the entorhinal cortex, not afflicting the primary visual cortex. Discussion: The aging rhesus macaque provides the long-sought animal model for exploring the etiology of late-onset Alzheimer's disease and for testing preventive strategies. (C) 2017 The Authors. Published by Elsevier Inc. on behalf of the Alzheimer's Association.
引用
收藏
页码:680 / 691
页数:12
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