Apoptosis in oligodendrocytes is associated with axonal degeneration in P301L tau mice

被引:42
作者
Zehr, C [1 ]
Lewis, J [1 ]
McGowan, E [1 ]
Crook, J [1 ]
Lin, WL [1 ]
Godwin, K [1 ]
Knight, J [1 ]
Dickson, DW [1 ]
Hutton, M [1 ]
机构
[1] Mayo Clin, Neurogen Neurotransgen & Neuropathol Labs, Jacksonville, FL 32224 USA
关键词
cell death; tau; tauopathy; TUNEL; caspase-3; Alzheimer's disease; frontotemporal dementia with parkinsonism linked to chromosome-17;
D O I
10.1016/j.nbd.2003.12.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Transgenic mice overexpressing human tau with the P301L mutation develop neurofibrillary tangles, extensive gliosis, adult-onset motor abnormalities, and neuronal loss in affected brain regions. We investigated the mechanism of neuronal cell death in this model of tauopathy. There was no evidence of neuronal apoptosis at any age; however, a population of oligodendorocytes was immunopositive for TUNEL and activated caspase-3. EM confirmed that these oligodendrocytes were undergoing apoptosis. These data suggest that classical apoptosis is not a major mechanism of neuronal cell death associated with the tau dysfunction in this mouse model; however, prominent white matter pathology in the spinal cord suggests that axonal degeneration in dying neurons causes oligodendrocytes to undergo apoptosis. It is unknown if loss of oligodendrocytes either through apoptosis or through the formation of intracellular tau lesions further contributes to the neurodegeneration seen in these mice. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:553 / 562
页数:10
相关论文
共 25 条
[1]  
Allen B, 2002, J NEUROSCI, V22, P9340
[2]   Morphological and biochemical assessment of DNA damage and apoptosis in Down syndrome and Alzheimer disease, and effect of postmortem tissue archival on TUNEL [J].
Anderson, AJ ;
Stoltzner, S ;
Lai, F ;
Su, J ;
Nixon, RA .
NEUROBIOLOGY OF AGING, 2000, 21 (04) :511-524
[3]   Oligodendroglial apoptosis occurs along degenerating axons and is associated with Fas and p75 expression following spinal cord injury in the rat [J].
Casha, S ;
Yu, WR ;
Fehlings, MG .
NEUROSCIENCE, 2001, 103 (01) :203-218
[4]   Neurobehavioral development of two mouse lines commonly used in transgenic studies [J].
Dierssen, M ;
Fotaki, V ;
de Lagrán, MM ;
Gratacós, M ;
Arbonés, M ;
Fillat, C ;
Estivill, X .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 73 (01) :19-25
[5]   Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference [J].
Foster, NL ;
Wilhelmsen, K ;
Sima, AAF ;
Jones, MZ ;
DAmato, CJ ;
Gilman, S ;
Spillantini, MG ;
Lynch, T ;
Mayeux, RP ;
Gaskell, PC ;
Hulette, CM ;
PericakVance, MA ;
WelshBohmer, KA ;
Dickson, DW ;
Heutink, P ;
Kros, J ;
vanSwieten, JC ;
Arwert, F ;
Ghetti, MB ;
Murrell, J ;
Lannfelt, L ;
Hutton, M ;
Jones, M ;
Phelps, CH ;
Snyder, DS ;
Oliver, E ;
Ball, MJ ;
Cummings, JL ;
Miller, BL ;
Katzman, R ;
Reed, L ;
Schelper, RL ;
Landska, DJ ;
Brun, A ;
Fink, JK ;
Kuhl, DE ;
Knopman, DS ;
Wszolek, Z ;
Miller, CA ;
Bird, TD ;
Lendon, C ;
Elechi, C .
ANNALS OF NEUROLOGY, 1997, 41 (06) :706-715
[6]   IMMUNOCHEMICAL AND IMMUNOHISTOCHEMICAL STUDY OF CARBONIC ANHYDRASE-II IN ADULT-RAT CEREBELLUM - A MARKER FOR OLIGODENDROCYTES [J].
GHANDOUR, MS ;
LANGLEY, OK ;
VINCENDON, G ;
GOMBOS, G ;
FILIPPI, D ;
LIMOZIN, N ;
DALMASSO, C ;
LAURENT, G .
NEUROSCIENCE, 1980, 5 (03) :559-&
[7]  
GOLD R, 1994, LAB INVEST, V71, P219
[8]   Transgenic mouse model of tauopathies with glial pathology and nervous system degeneration [J].
Higuchi, M ;
Ishihara, T ;
Zhang, B ;
Hong, M ;
Andreadis, A ;
Trojanowski, JQ ;
Lee, VMY .
NEURON, 2002, 35 (03) :433-446
[9]  
Jellinger K. A., 2000, Journal of Neural Transmission Supplement, V60, P21
[10]   APOPTOSIS - BASIC BIOLOGICAL PHENOMENON WITH WIDE-RANGING IMPLICATIONS IN TISSUE KINETICS [J].
KERR, JFR ;
WYLLIE, AH ;
CURRIE, AR .
BRITISH JOURNAL OF CANCER, 1972, 26 (04) :239-+