The ultrastructural distribution of alpha-synuclein-like protein in normal mouse brain

被引:57
作者
Totterdell, S
Hanger, D
Meredith, GE
机构
[1] Univ Oxford, Dept Pharmacol, Oxford OX1 3QT, England
[2] Kings Coll London, Inst Psychiat, London SE5 8AF, England
[3] Finch Univ Hlth Sci Chicago Med Sch, Dept Cellular & Mol Pharmacol, N Chicago, IL 60064 USA
关键词
synaptic; electron microscope; immunocytochemistry; basal ganglia; substantia nigra; hippocampus;
D O I
10.1016/j.brainres.2003.10.072
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The synaptic protein alpha-synuclein is found throughout the brain, although its function remains ill-defined. Abnormal accumulations of alpha-synuclein have been recognised to be associated with a number of neurodegenerative diseases, including Alzheimer's disease and Parkinson's disease. Nevertheless, little is known about the precise localisation of this protein within the normal brain, information which might contribute to our understanding of its role in both health and disease. We raised an antibody which recognises both human and murine alpha-synuclein and this was used to Study the distribution of the protein in the normal mouse brain. We used morphological characteristics to classify the immunopositive presynaptic elements and their targets. We conclude that the protein is present in synaptic boutons of axons with different neurochemical phenotypes but that it is not present in all synaptic terminals. Furthermore, the protein is present in the terminals of neurons such as the dopaminergic neurons of the substantia nigra and the glutamatergic neurons of the hippocampus, cell types which accumulate alpha-synuclein in disease. Nevertheless alpha-synuclein is also found in terminals of neurons which have not been reported to accumulate the protein in neurodegenerative disorders. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 72
页数:12
相关论文
共 57 条
[1]   Mice lacking α-synuclein display functional deficits in the nigrostriatal dopamine system [J].
Abeliovich, A ;
Schmitz, Y ;
Fariñas, I ;
Choi-Lundberg, D ;
Ho, WH ;
Castillo, PE ;
Shinsky, N ;
Verdugo, JMG ;
Armanini, M ;
Ryan, A ;
Hynes, M ;
Phillips, H ;
Sulzer, D ;
Rosenthal, A .
NEURON, 2000, 25 (01) :239-252
[2]  
Alheid George F., 1995, P495
[3]  
Amaral David G., 1995, P443
[4]   NACP/α-synuclein and tau constitute two distinctive subsets of filaments in the same neuronal inclusions in brains from a family of parkinsonism and dementia with Lewy bodies:: double-immunolabeling fluorescence and electron microscopic studies [J].
Arima, K ;
Mizutani, T ;
Alim, MA ;
Tonozuka-Uehara, H ;
Izumiyama, Y ;
Hirai, S ;
Uéda, K .
ACTA NEUROPATHOLOGICA, 2000, 100 (02) :115-121
[5]  
Baba M, 1998, AM J PATHOL, V152, P879
[6]   CONVERGENT SYNAPTIC INPUT FROM THE NEOSTRIATUM AND THE SUBTHALAMUS ONTO IDENTIFIED NIGROTHALAMIC NEURONS IN THE RAT [J].
BEVAN, MD ;
BOLAM, JP ;
CROSSMAN, AR .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1994, 6 (03) :320-334
[7]  
Braak E, 2001, ACTA NEUROPATHOL, V101, P195
[8]   Extensive axonal Lewy neurites in Parkinson's disease:: a novel pathological feature revealed by α-synuclein immunocytochemistry [J].
Braak, H ;
Sandmann-Keil, D ;
Gai, WP ;
Braak, E .
NEUROSCIENCE LETTERS, 1999, 265 (01) :67-69
[9]   Alpha-synuclein is not a requisite component of synaptic boutons in the adult human central nervous system [J].
Braak, H ;
Del Tredici, K ;
Gai, WP ;
Braak, E .
JOURNAL OF CHEMICAL NEUROANATOMY, 2000, 20 (3-4) :245-252
[10]  
Clayton DF, 1999, J NEUROSCI RES, V58, P120, DOI 10.1002/(SICI)1097-4547(19991001)58:1<120::AID-JNR12>3.0.CO