Stereologic analysis of neurofibrillary tangle formation in prefrontal cortex area 9 in aging and Alzheimer's disease

被引:96
作者
Bussière, T
Gold, G
Kövari, E
Giannakopoulos, P
Bouras, C
Perl, DP
Morrison, JH
Hof, PR
机构
[1] CUNY Mt Sinai Sch Med, Kastor Neurobiol Aging Lab, New York, NY 10029 USA
[2] CUNY Mt Sinai Sch Med, Fishberg Res Ctr Neurobiol, New York, NY 10029 USA
[3] CUNY Mt Sinai Sch Med, Dept Geriatr & Adult Dev, New York, NY 10029 USA
[4] CUNY Mt Sinai Sch Med, Dept Ophthalmol, New York, NY 10029 USA
[5] CUNY Mt Sinai Sch Med, Dept Pathol Neuropathol, New York, NY 10029 USA
[6] CUNY Mt Sinai Sch Med, Dept Psychiat, New York, NY 10029 USA
[7] Elan Pharmaceut Inc, San Francisco, CA 94080 USA
[8] Univ Geneva, Clin Geriatr Psychiat, HUG Belle Idee, Sch Med, Geneva, Switzerland
[9] Univ Geneva, Dept Geriatr, HUG Belle Idee, Sch Med, Geneva, Switzerland
[10] Univ Lausanne, Sch Med, Dept Psychogeriatr, Prilly, Switzerland
关键词
brain aging; dementia; neocortex; pyramidal neuron; quantitative neuropathology; stereology;
D O I
10.1016/S0306-4522(02)00942-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is characterized neuro-pathologically by several features including extensive neuronal death in the cerebral cortex. In fact, while neuropathological changes restricted to the hippocampal formation are a consistent reflection of age-related memory impairment, overt dementia is present only in cases with neocortical involvement. Several quantitative studies have reported a substantial loss of neurons from these regions and a parallel increase in the number of neurofibrillary tangles (NFT). However, accurate quantitative data on the dynamics of NFT formation are lacking. In the present study, we performed a stereologic analysis of the proportions of intracellular and extracellular (ghost) NFT, and unaffected neurons in the deep part of layer III (layer IIIc) and the superficial part of layer V (layer Va) of Brodmann's prefrontal cortex area 9. Elderly cognitively unimpaired cases were compared with cases with different degrees of cognitive dysfunction. The data revealed differential rates of formation of intracellular and extracellular NFT between the two layers, and confirmed the presence of a severe disease-associated, but not age-related, neuronal loss. It was also shown that a susbtantial number of pyramidal cells may persist either unaffected or in a transitional stage of NFT formation in both neocortical layers. These results suggest that a considerable number of neurons containing an intracellular NFT exists in the neocortex until late in the course of AD. Whereas it is not possible to assess whether such transitional neurons are fully functional, these affected neurons might respond positively to therapeutic strategies aimed at protecting the cells that are prone to neurofibrillary degeneration in AD. (C) 2003 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:577 / 592
页数:16
相关论文
共 81 条
[1]   The Topographical and Neuroanatomical Distribution of Neurofibrillary Tangles and Neuritic Plaques in the Cerebral Cortex of Patients with Alzheimer's Disease [J].
Arnold, Steven E. ;
Hyman, Bradley T. ;
Flory, Jill ;
Damasio, Antonio R. ;
Van Hoesen, Gary W. .
CEREBRAL CORTEX, 1991, 1 (01) :103-116
[2]   Specific tau phosphorylation sites correlate with severity of neuronal cytopathology in Alzheimer's disease [J].
Augustinack, JC ;
Schneider, A ;
Mandelkow, EM ;
Hyman, BT .
ACTA NEUROPATHOLOGICA, 2002, 103 (01) :26-35
[3]   NEOCORTICAL NEUROFIBRILLARY TANGLES CORRELATE WITH DEMENTIA SEVERITY IN ALZHEIMERS-DISEASE [J].
BIERER, LM ;
HOF, PR ;
PUROHIT, DP ;
CARLIN, L ;
SCHMEIDLER, J ;
DAVIS, KL ;
PERL, DP .
ARCHIVES OF NEUROLOGY, 1995, 52 (01) :81-88
[4]   NEUROFIBRILLARY TANGLE DENSITIES IN THE HIPPOCAMPAL-FORMATION IN A NONDEMENTED POPULATION DEFINE SUBGROUPS OF PATIENTS WITH DIFFERENTIAL EARLY PATHOLOGICAL-CHANGES [J].
BOURAS, C ;
HOF, PR ;
MORRISON, JH .
NEUROSCIENCE LETTERS, 1993, 153 (02) :131-135
[5]   REGIONAL DISTRIBUTION OF NEUROFIBRILLARY TANGLES AND SENILE PLAQUES IN THE CEREBRAL-CORTEX OF ELDERLY PATIENTS - A QUANTITATIVE-EVALUATION OF A ONE-YEAR AUTOPSY POPULATION FROM A GERIATRIC HOSPITAL [J].
BOURAS, C ;
HOF, PR ;
GIANNAKOPOULOS, P ;
MICHEL, JP ;
MORRISON, JH .
CEREBRAL CORTEX, 1994, 4 (02) :138-150
[6]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[7]  
Brodmann K, 1909, VERGLEICHENDE LOKALI
[8]   Tau protein isoforms, phosphorylation and role in neurodegenerative disorders [J].
Buée, L ;
Bussière, T ;
Buée-Scherrer, V ;
Delacourte, A ;
Hof, PR .
BRAIN RESEARCH REVIEWS, 2000, 33 (01) :95-130
[9]   AD2, a phosphorylation-dependent monoclonal antibody directed against tau proteins found in Alzheimer's disease [J].
BueeScherrer, V ;
Condamines, O ;
MourtonGilles, C ;
Jakes, R ;
Goedert, M ;
Pau, B ;
Delacourte, A .
MOLECULAR BRAIN RESEARCH, 1996, 39 (1-2) :79-88
[10]   Stereologic assessment of the total cortical volume occupied by amyloid deposits and its relationship with cognitive status in aging and Alzheimer's disease [J].
Bussière, T ;
Friend, PD ;
Sadeghi, N ;
Wicinski, B ;
Lin, GI ;
Bouras, C ;
Giannakopoulos, P ;
Robakis, NK ;
Morrison, JH ;
Perl, DP ;
Hof, PR .
NEUROSCIENCE, 2002, 112 (01) :75-91