Mitochondria: The Next (Neurode)Generation

被引:448
作者
Schon, Eric A. [1 ,2 ,4 ,5 ]
Przedborski, Serge [1 ,3 ,4 ]
机构
[1] Columbia Univ, Dept Neurol, New York, NY 10032 USA
[2] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
[3] Columbia Univ, Dept Pathol & Cell Biol, New York, NY 10032 USA
[4] Columbia Univ, Ctr Motor Neuron Biol & Dis, New York, NY 10032 USA
[5] Columbia Univ, H Houston Merritt Clin Res Ctr, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
MARIE-TOOTH-DISEASE; HEREDITARY SPASTIC PARAPLEGIA; AMYOTROPHIC-LATERAL-SCLEROSIS; M-AAA PROTEASE; SUBSTANTIA-NIGRA NEURONS; KINESIN HEAVY-CHAIN; ALZHEIMERS-DISEASE; ENDOPLASMIC-RETICULUM; PARKINSONS-DISEASE; MUTANT HUNTINGTIN;
D O I
10.1016/j.neuron.2011.06.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adult-onset neurodegenerative disorders are disabling and often fatal diseases of the nervous system whose underlying mechanisms of cell death remain unknown. Defects in mitochondrial respiration had previously been proposed to contribute to the occurrence of many, if not all, of the most common neurodegenerative disorders. However, the discovery of genes mutated in hereditary forms of these enigmatic diseases has additionally suggested defects in mitochondria! dynamics. Such disturbances can lead to changes in mitochondrial trafficking, in interorganellar communication, and in mitochondrial quality control. These new mechanisms by which mitochondria may also be linked to neurodegeneration will likely have far-reaching implications for our understanding of the pathophysiology and treatment of adult-onset neurodegenerative disorders.
引用
收藏
页码:1033 / 1053
页数:21
相关论文
共 158 条
[81]   The hereditary spastic paraplegia protein spartin localises to mitochondria [J].
Lu, JianPing ;
Rashid, Faiza ;
Byrne, Paula C. .
JOURNAL OF NEUROCHEMISTRY, 2006, 98 (06) :1908-1919
[82]   Rapamycin Protects against Neuron Death in In Vitro and In Vivo Models of Parkinson's Disease [J].
Malagelada, Cristina ;
Jin, Zong Hao ;
Jackson-Lewis, Vernice ;
Przedborski, Serge ;
Greene, Lloyd A. .
JOURNAL OF NEUROSCIENCE, 2010, 30 (03) :1166-1175
[83]   The role of ZFYVE27/protrudin in hereditary spastic paraplegia [J].
Martignoni, Monica ;
Riano, Elena ;
Rugarli, Elena I. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 83 (01) :127-128
[84]   Mutations of optineurin in amyotrophic lateral sclerosis [J].
Maruyama, Hirofumi ;
Morino, Hiroyuki ;
Ito, Hidefumi ;
Izumi, Yuishin ;
Kato, Hidemasa ;
Watanabe, Yasuhito ;
Kinoshita, Yoshimi ;
Kamada, Masaki ;
Nodera, Hiroyuki ;
Suzuki, Hidenori ;
Komure, Osamu ;
Matsuura, Shinya ;
Kobatake, Keitaro ;
Morimoto, Nobutoshi ;
Abe, Koji ;
Suzuki, Naoki ;
Aoki, Masashi ;
Kawata, Akihiro ;
Hirai, Takeshi ;
Kato, Takeo ;
Ogasawara, Kazumasa ;
Hirano, Asao ;
Takumi, Toru ;
Kusaka, Hirofumi ;
Hagiwara, Koichi ;
Kaji, Ryuji ;
Kawakami, Hideshi .
NATURE, 2010, 465 (7295) :223-U109
[85]   Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation [J].
McDermott, CJ ;
Grierson, AJ ;
Wood, JD ;
Bingley, M ;
Wharton, SB ;
Bushby, KMD ;
Shaw, PJ .
ANNALS OF NEUROLOGY, 2003, 54 (06) :748-759
[86]   Identification of novel spartin-interactors shows spartin is a multifunctional protein [J].
Milewska, Malgorzata ;
McRedmond, James ;
Byrne, Paula Catherine .
JOURNAL OF NEUROCHEMISTRY, 2009, 111 (04) :1022-1030
[87]   Alsin is partially associated with centrosome in human cells [J].
Millecamps, S ;
Gentil, BJ ;
Gros-Louis, F ;
Rouleau, G ;
Julien, JP .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2005, 1745 (01) :84-100
[88]   Mitofusin 2 Is Necessary for Transport of Axonal Mitochondria and Interacts with the Miro/Milton Complex [J].
Misko, Albert ;
Jiang, Sirui ;
Wegorzewska, Iga ;
Milbrandt, Jeffrey ;
Baloh, Robert H. .
JOURNAL OF NEUROSCIENCE, 2010, 30 (12) :4232-4240
[89]   Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stress [J].
Moore, DJ ;
Zhang, L ;
Troncoso, J ;
Lee, MK ;
Hattori, N ;
Mizuno, Y ;
Dawson, TM ;
Dawson, VL .
HUMAN MOLECULAR GENETICS, 2005, 14 (01) :71-84
[90]   Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2 [J].
Moreira, MC ;
Klur, S ;
Watanabe, M ;
Németh, AH ;
Le Ber, I ;
Moniz, JC ;
Tranchant, C ;
Aubourg, P ;
Tazir, M ;
Schöls, L ;
Pandolfo, M ;
Schulz, JB ;
Pouget, J ;
Calvas, P ;
Shizuka-Ikeda, M ;
Shoji, M ;
Tanaka, M ;
Izatt, L ;
Shaw, CE ;
M'Zahem, A ;
Dunne, E ;
Bomont, P ;
Benhassine, T ;
Bouslam, N ;
Stevanin, G ;
Brice, A ;
Guimaraes, J ;
Mendonça, P ;
Barbot, C ;
Coutinho, P ;
Sequeiros, J ;
Dürr, A ;
Warter, JM ;
Koenig, M .
NATURE GENETICS, 2004, 36 (03) :225-227