Protein misfolding disorders and macroautophagy

被引:108
作者
Menzies, Fiona M. [1 ]
Moreau, Kevin [1 ]
Rubinsztein, David C. [1 ]
机构
[1] Univ Cambridge, Dept Med Genet, Cambridge Inst Med Res, Cambridge CB 0XY, England
基金
英国惠康基金;
关键词
FAMILIAL ALZHEIMERS-DISEASE; AGGREGATE-PRONE PROTEINS; AMYOTROPHIC-LATERAL-SCLEROSIS; AUTOPHAGY-MEDIATED CLEARANCE; MOTOR-NEURON DISEASE; HUNTINGTONS-DISEASE; ALPHA-SYNUCLEIN; MOUSE MODEL; MUTANT HUNTINGTIN; PARKINSONS-DISEASE;
D O I
10.1016/j.ceb.2010.10.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A large group of diseases, termed protein misfolding disorders, share the common feature of the accumulation of misfolded proteins. The possibility of a common mechanism underlying either the pathogenesis or therapy for these diseases is appealing. Thus, there is great interest in the role of protein degradation via autophagy in such conditions where the protein is found in the cytoplasm. Here we review the growing evidence supporting a role for autophagic dysregulation as a contributing factor to protein accumulation and cellular toxicity in certain protein misfolding disorders and discuss the available evidence that upregulation of autophagy may be a valuable therapeutic strategy.
引用
收藏
页码:190 / 197
页数:8
相关论文
共 83 条
[11]   Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation [J].
Davies, SW ;
Turmaine, M ;
Cozens, BA ;
DiFiglia, M ;
Sharp, AH ;
Ross, CA ;
Scherzinger, E ;
Wanker, EE ;
Mangiarini, L ;
Bates, GP .
CELL, 1997, 90 (03) :537-548
[12]   Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2 [J].
Ferguson, Cole J. ;
Lenk, Guy M. ;
Meisler, Miriam H. .
HUMAN MOLECULAR GENETICS, 2009, 18 (24) :4868-4878
[13]   Lithium delays progression of amyotrophic lateral sclerosis [J].
Fornai, Francesco ;
Longone, Patrizia ;
Cafaro, Luisa ;
Kastsiuchenka, Olga ;
Ferrucci, Michela ;
Manca, Maria Laura ;
Lazzeri, Gloria ;
Spalloni, Alicia ;
Bellio, Natascia ;
Lenzi, Paola ;
Modugno, Nicola ;
Siciliano, Gabriele ;
Isicloro, Ciro ;
Murri, Luigi ;
Ruggieri, Stefano ;
Paparelli, Antonio .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (06) :2052-2057
[14]   PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1 [J].
Geisler, Sven ;
Holmstroem, Kira M. ;
Skujat, Diana ;
Fiesel, Fabienne C. ;
Rothfuss, Oliver C. ;
Kahle, Philipp J. ;
Springer, Wolfdieter .
NATURE CELL BIOLOGY, 2010, 12 (02) :119-U70
[15]   SEGREGATION OF A MISSENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE WITH FAMILIAL ALZHEIMERS-DISEASE [J].
GOATE, A ;
CHARTIERHARLIN, MC ;
MULLAN, M ;
BROWN, J ;
CRAWFORD, F ;
FIDANI, L ;
GIUFFRA, L ;
HAYNES, A ;
IRVING, N ;
JAMES, L ;
MANT, R ;
NEWTON, P ;
ROOKE, K ;
ROQUES, P ;
TALBOT, C ;
PERICAKVANCE, M ;
ROSES, A ;
WILLIAMSON, R ;
ROSSOR, M ;
OWEN, M ;
HARDY, J .
NATURE, 1991, 349 (6311) :704-706
[16]   Paradigms for the identification of new genes in motor neuron degeneration [J].
Hafezparast, M ;
Ahmad-Annuar, A ;
Hummerich, H ;
Shah, P ;
Ford, M ;
Baker, C ;
Bowen, S ;
Martin, JE ;
Fisher, EMC .
AMYOTROPHIC LATERAL SCLEROSIS, 2003, 4 (04) :249-257
[17]   Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice [J].
Hara, Taichi ;
Nakamura, Kenji ;
Matsui, Makoto ;
Yamamoto, Akitsugu ;
Nakahara, Yohko ;
Suzuki-Migishima, Rika ;
Yokoyama, Minesuke ;
Mishima, Kenji ;
Saito, Ichiro ;
Okano, Hideyuki ;
Mizushima, Noboru .
NATURE, 2006, 441 (7095) :885-889
[19]   Early autophagic response in a novel knock-in model of Huntington disease [J].
Heng, Mary Y. ;
Duong, Duy K. ;
Albin, Roger L. ;
Tallaksen-Greene, Sara J. ;
Hunter, Jesse M. ;
Lesort, Mathieu J. ;
Osmand, Alex ;
Paulson, Henry L. ;
Detloff, Peter J. .
HUMAN MOLECULAR GENETICS, 2010, 19 (19) :3702-3720
[20]   XBP-1 deficiency in the nervous system protects against amyotrophic lateral sclerosis by increasing autophagy [J].
Hetz, Claudio ;
Thielen, Peter ;
Matus, Soledad ;
Nassif, Melissa ;
Court, Felipe ;
Kiffin, Roberta ;
Martinez, Gabriela ;
Cuervo, Ana Maria ;
Brown, Robert H. ;
Glimcher, Laurie H. .
GENES & DEVELOPMENT, 2009, 23 (19) :2294-2306