Tau inclusions in retinal ganglion cells of human P301S tau transgenic mice: Effects on axonal viability

被引:98
作者
Gasparini, Laura [1 ]
Crowther, R. Anthony [2 ]
Martin, Keith R. [1 ]
Berg, Nicola [1 ]
Coleman, Michael [3 ]
Goedert, Michel [2 ]
Spillantini, Maria Grazia [1 ]
机构
[1] Univ Cambridge, Cambridge Ctr Brain Repair, Cambridge CB2 0PY, England
[2] MRC, Mol Biol Lab, Cambridge CB2 0QH, England
[3] Babraham Inst, Cambridge CB2 4AT, England
基金
英国医学研究理事会;
关键词
Tau; Retinal ganglion cells; Axonopathy; Tauopathy; Alzheimer disease; Frontotemporal dementia; ALZHEIMERS-DISEASE; NEUROFIBRILLARY TANGLES; PROTEIN-KINASE; AMYLOID-BETA; MOUSE MODEL; DEGENERATION; AXONOPATHY; PATHOLOGY; NEURODEGENERATION; PHOSPHORYLATION;
D O I
10.1016/j.neurobiolaging.2009.03.002
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Tau inclusions play a key role in the pathogenesis of tauopathies. Altered tau levels have been detected in retina and optic nerve of patients with glaucoma, suggesting the possibility of shared pathogenic mechanisms with tauopathies. Here we report that hyperphosphorylated transgenic tau accumulates in the nerve fibre layer and, from 2 months of age, aggregates into filamentous inclusions in retinal ganglion cells of human P301S tau transgenic mice. Axonopathy and accumulation of hyperphosphorylated tau in the nerve fibre layer preceded inclusion formation. Hyperphosphorylated tau and tau inclusions were also detected in cultured retinal explants from 5-month-old transgenic mice. Axonal outgrowth was similar in transgenic and wild-type retinal explants under basal conditions. However, when exposed to growth-promoting stimuli, axon elongation was enhanced in explants from wild-type but not transgenic mice, indicating that the presence of abnormal tau can impair stimulated axonal outgrowth. These findings suggest that the retina is a good model system for investigating tau-driven neurodegeneration and for assessing potential pharmacological modifiers for tauopathies. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:419 / 433
页数:15
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