Deregulation of autophagy in postmortem brains of Machado-Joseph disease patients

被引:42
作者
Sittler, Annie [1 ]
Muriel, Marie-Paule [1 ]
Marinello, Martina [1 ]
Brice, Alexis [1 ,2 ]
den Dunnen, Wilfred [3 ]
Alves, Sandro [1 ]
机构
[1] UPMC Univ Paris 06, Sorbonne Univ, Pitie Salpetriere Hosp,ICM Brain & Spine Inst, INSERM,U1127,CNRS,UMR 7225,UMR S 1127, F-75013 Paris, France
[2] GH Pitie Salpetriere, AP HP, Dept Genet & Cytogenet, Paris, France
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, Groningen, Netherlands
关键词
ataxin-3; autophagy; cerebellum; Machado-Joseph disease (MJD) patients; postmortem; SPINOCEREBELLAR ATAXIA TYPE-3; DOMINANT CEREBELLAR-ATAXIA; NEURONAL INTRANUCLEAR INCLUSIONS; KNOCK-IN MICE; JAPANESE FAMILY; NERVOUS-SYSTEM; PROTEIN; SCA3; CELLS; P62/SQSTM1;
D O I
10.1111/neup.12433
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Autophagy, the major pathway for protein turnover, is critical to maintain cellular homeostasis and has been implicated in neurodegenerative diseases. The aim of this research was to analyze the expression of autophagy markers in postmortem brains from Machado-Joseph disease (MJD) patients. The expression of autophagy markers in the cerebellum and the oculomotor nucleus from MJD patients and age-matched controls with no signs of neuropathology was inspected postmortem by immunohistochemistry (IHC) and Western blot. Furthermore, autophagy was examined by means of transmission electron microscopy (TEM). Western blot and IHC revealed nuclear accumulation of misfolded ataxin-3 (ATXN3) and the presence of ubiquitin- and p62-positive aggregates in MJD patients as compared to controls. Moreover, the autophagic proteins, autophagy-related gene (Atg) protein (ATG)-7, ATG-12, ATG16L2 and autophagosomal microtubule-associated protein light chain 3 (LC3) were significantly increased in MJD brains relative to controls, while beclin-1 levels were reduced in MJD patients. Increase in the levels of lysosomal-associated membrane protein 2 (LAMP-2) and of the endosomal markers (Rab7 and Rab1A) were observed in MJD patients relatively to controls. In addition, these findings were further confirmed by TEM in brain tissue where large vesicles accumulating electron-dense materials were highly enriched in MJD patients. Postmortem brains with MJD exhibit increased markers of autophagy relative to age-matched control brains, therefore suggesting strong dysregulation of autophagy that may have an important role in the course of MJD pathogenesis.
引用
收藏
页码:113 / 124
页数:12
相关论文
共 52 条
  • [1] Autosomal dominant cerebellar ataxia type I -: Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3
    Abele, M
    Bürk, K
    Andres, F
    Topka, H
    Laccone, F
    Bösch, S
    Brice, A
    Cancel, G
    Dichgans, J
    Klockgether, T
    [J]. BRAIN, 1997, 120 : 2141 - 2148
  • [2] Striatal and nigral pathology in a lentiviral rat model of Machado-Joseph disease
    Alves, Sandro
    Regulier, Etienne
    Nascimento-Ferreira, Isabel
    Hassig, Raymonde
    Dufour, Noelle
    Koeppen, Arnulf
    Carvalho, Ana Luisa
    Simoes, Sergio
    Pedroso de Lima, Maria C.
    Brouillet, Emmanuel
    Gould, Veronica Colomer
    Deglon, Nicole
    de Almeida, Luis Pereira
    [J]. HUMAN MOLECULAR GENETICS, 2008, 17 (14) : 2071 - 2083
  • [3] The autophagy/lysosome pathway is impaired in SCA7 patients and SCA7 knock-in mice
    Alves, Sandro
    Cormier-Dequaire, Florence
    Marinello, Martina
    Marais, Thibaut
    Muriel, Marie-Paule
    Beaumatin, Florian
    Charbonnier-Beaupel, Fanny
    Tahiri, Khadija
    Seilhean, Danielle
    El Hachimi, Khalid
    Ruberg, Merle
    Stevanin, Giovanni
    Barkats, Martine
    den Dunnen, Wilfred
    Priault, Muriel
    Brice, Alexis
    Durr, Alexandra
    Corvol, Jean-Christophe
    Sittler, Annie
    [J]. ACTA NEUROPATHOLOGICA, 2014, 128 (05) : 705 - 722
  • [4] Polyglutamine tracts regulate beclin 1-dependent autophagy
    Ashkenazi, Avraham
    Bento, Carla F.
    Ricketts, Thomas
    Vicinanza, Mariella
    Siddiqi, Farah
    Pavel, Mariana
    Squitieri, Ferdinando
    Hardenberg, Maarten C.
    Imarisio, Sara
    Menzies, Fiona M.
    Rubinsztein, David C.
    [J]. NATURE, 2017, 545 (7652) : 108 - +
  • [5] Defining the role of ubiquitin-interacting motifs in the polyglutamine disease protein, ataxin-3
    Berke, SJS
    Chai, YH
    Marrs, GL
    Wen, H
    Paulson, HL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (36) : 32026 - 32034
  • [6] p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death
    Bjorkoy, G
    Lamark, T
    Brech, A
    Outzen, H
    Perander, M
    Overvatn, A
    Stenmark, H
    Johansen, T
    [J]. JOURNAL OF CELL BIOLOGY, 2005, 171 (04) : 603 - 614
  • [7] Autosomal dominant cerebellar ataxia type I:: oculomotor abnormalities in families with SCA1, SCA2, and SCA3
    Bürk, K
    Fetter, M
    Abele, M
    Laccone, F
    Brice, A
    Dichgans, J
    Klockgether, T
    [J]. JOURNAL OF NEUROLOGY, 1999, 246 (09) : 789 - 797
  • [8] Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice
    Chort, Alice
    Alves, Sandro
    Marinello, Martina
    Dufresnois, Beatrice
    Dornbierer, Jean-Gabriel
    Tesson, Christelle
    Latouche, Morwena
    Baker, Darren P.
    Barkats, Martine
    El Hachimi, Khalid H.
    Ruberg, Merle
    Janer, Alexandre
    Stevanin, Giovanni
    Brice, Alexis
    Sittler, Annie
    [J]. BRAIN, 2013, 136 : 1732 - 1745
  • [9] Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies
    Ciechanover, Aaron
    Kwon, Yong Tae
    [J]. EXPERIMENTAL AND MOLECULAR MEDICINE, 2015, 47 : e147 - e147
  • [10] Autophagy: in sickness and in health
    Cuervo, AM
    [J]. TRENDS IN CELL BIOLOGY, 2004, 14 (02) : 70 - 77