Intranuclear aggregation of nonexpanded ataxin-3 in Marinesco bodies of the nonhuman primate substantia nigra

被引:22
作者
Kettner, M [1 ]
Willwohl, D
Hubbard, GB
Rüb, U
Dick, EJ
Cox, AB
Trottier, Y
Auburger, G
Braak, H
Schultz, C
机构
[1] Goethe Univ Frankfurt, Dept Anat, D-60590 Frankfurt, Germany
[2] SW Fdn Biomed Res, Dept Lab Anim Med, San Antonio, TX USA
[3] SW Fdn Biomed Res, SW Reg Primate Res Ctr, San Antonio, TX USA
[4] Wilford Hall USAF Med Ctr, Clin Res Squadron, Lackland AFB, TX 78236 USA
[5] USAF, Res Lab, Direct Energy Div, Brooks AFB, TX USA
[6] Univ Strasbourg 1, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
[7] Goethe Univ Frankfurt, Dept Neurol, Sect Mol Neurogenet, D-60590 Frankfurt, Germany
关键词
ataxin-3; polyglutamine disease; ubiquitin; intranuclear inclusion; nonhuman primates; Marinesco bodies; spinocerebellar ataxia;
D O I
10.1006/exnr.2002.7916
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Marinesco bodies (MB) are intranuclear inclusion bodies predominantly found in melanin-pigmented neurons of the substantia nigra. MB are demonstrable not only in humans but also in nonhuman primates. In the present study MB of aged rhesus monkeys (Macaca mulatta; n = 15; mean age 16 years) and aged baboons (Papio anubis; n = 13; mean age 25 years) were examined immunohistochemically. MB were found to be immunoreactive for ubiquitin, a protein involved in initiation of proteasome-mediated proteolysis. We also demonstrate that MB in monkeys are intensely immunoreactive for the protein ataxin-3 as detected by using two monoclonal anti-ataxin-3 antibodies (1H9 and 2B6). The abnormally expanded form of this polyglutamine protein is known to be causally involved in spinocerebellar ataxia type 3 or Machado-Joseph disease. The monoclonal antibody 1C2 was employed to examine whether ataxin-3 in MB in monkeys contains such an abnormally expanded polyglutamine stretch. MB were consistently 1C2-immunonegative, indicating that they are composed of normal wild-type ataxin-3. In conclusion MB in nonhuman primates permit experimental examination of mechanisms involved in transnuclear localization, intranuclear aggregation, and ubiquitination of nonexpanded polyglutamine proteins. (C) 2002 Elsevier Science (USA).
引用
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页码:117 / 121
页数:5
相关论文
共 24 条
[1]   Ubiquitin, cellular inclusions and their role in neurodegeneration [J].
Alves-Rodrigues, A ;
Gregori, L ;
Figueiredo-Pereira, ME .
TRENDS IN NEUROSCIENCES, 1998, 21 (12) :516-520
[2]   Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice [J].
Cummings, CJ ;
Reinstein, E ;
Sun, YL ;
Antalffy, B ;
Jiang, YH ;
Ciechanover, A ;
Orr, HT ;
Beaudet, AL ;
Zoghbi, HY .
NEURON, 1999, 24 (04) :879-892
[3]  
DICKSON DW, 1990, LAB INVEST, V63, P87
[4]   Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain [J].
DiFiglia, M ;
Sapp, E ;
Chase, KO ;
Davies, SW ;
Bates, GP ;
Vonsattel, JP ;
Aronin, N .
SCIENCE, 1997, 277 (5334) :1990-1993
[5]   Cell death in polyglutamine diseases [J].
Evert, BO ;
Wüllner, U ;
Klockgether, T .
CELL AND TISSUE RESEARCH, 2000, 301 (01) :189-204
[6]   Ataxin-3 is translocated into the nucleus for the formation of intranuclear inclusions in normal and Machado-Joseph disease brains [J].
Fujigasaki, H ;
Uchihara, T ;
Koyano, S ;
Iwabuchi, K ;
Yagishita, S ;
Makifuchi, T ;
Nakamura, A ;
Ishida, K ;
Toru, S ;
Hirai, S ;
Ishikawa, K ;
Tanabe, T ;
Mizusawa, H .
EXPERIMENTAL NEUROLOGY, 2000, 165 (02) :248-256
[7]   Preferential recruitment of ataxin-3 independent of expanded polyglutamine: an immunohistochemical study on Marinesco bodies [J].
Fujigasaki, H ;
Uchihara, T ;
Takahashi, J ;
Matsushita, H ;
Nakamura, A ;
Koyano, S ;
Iwabuchi, K ;
Hirai, S ;
Mizusawa, H .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2001, 71 (04) :518-520
[8]   CAG EXPANSIONS IN A NOVEL GENE FOR MACHADO-JOSEPH DISEASE AT CHROMOSOME 14Q32.1 [J].
KAWAGUCHI, Y ;
OKAMOTO, T ;
TANIWAKI, M ;
AIZAWA, M ;
INOUE, M ;
KATAYAMA, S ;
KAWAKAMI, H ;
NAKAMURA, S ;
NISHIMURA, M ;
AKIGUCHI, I ;
KIMURA, J ;
NARUMIYA, S ;
KAKIZUKA, A .
NATURE GENETICS, 1994, 8 (03) :221-228
[9]   Ataxin-1 nuclear localization and aggregation:: Role in polyglutamine-induced disease in SCA1 transgenic mice [J].
Klement, IA ;
Skinner, PJ ;
Kaytor, MD ;
Yi, H ;
Hersch, SM ;
Clark, HB ;
Zoghbi, HY ;
Orr, HT .
CELL, 1998, 95 (01) :41-53
[10]  
Klockgether T, 2000, MOVEMENT DISORD, V15, P604, DOI 10.1002/1531-8257(200007)15:4<604::AID-MDS1004>3.0.CO