An amyloid-like cascade hypothesis for C9orf72 ALS/FTD

被引:57
作者
Edbauer, Dieter [1 ,2 ,3 ]
Haass, Christian [1 ,2 ,4 ]
机构
[1] German Ctr Neurodegenerat Dis DZNE, Feodor Lynen Str 17, D-81377 Munich, Germany
[2] Munich Cluster Syst Neurol SyNergy, Feodor Lynen Str 17, D-81377 Munich, Germany
[3] Univ Munich, D-81377 Munich, Germany
[4] Univ Munich, Biomed Ctr BMC, Feodor Lynen Str 17, D-81377 Munich, Germany
基金
欧洲研究理事会;
关键词
FRONTOTEMPORAL LOBAR DEGENERATION; AMYOTROPHIC-LATERAL-SCLEROSIS; DIPEPTIDE REPEAT PROTEINS; NUCLEAR-RNA FOCI; HEXANUCLEOTIDE REPEAT; EXPANDED C9ORF72; MOTOR-NEURONS; ANTISENSE TRANSCRIPTS; ALZHEIMERS-DISEASE; TARDBP MUTATIONS;
D O I
10.1016/j.conb.2015.10.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Expansion of a GGGGCC repeat in C9orf72 causes amyotrophic lateral sclerosis, frontotemporal dementia, or a combination of both. Bidirectional repeat transcripts sequester RNA-binding proteins into nuclear RNA foci. The repeat is translated into dipeptide repeat (DPR) proteins that are crucial for repeat-induced toxicity. DPRs inhibit the proteasome and sequester other proteins. These changes are accompanied by widespread brain atrophy and subclinical cognitive impairment before disease onset. Both repeat RNA and DPRs impair nucleocytoplasmic transport and promote TDP-43 mislocalization and aggregation. Thus, repeat RNA and DPRs may gradually trigger TDP-43 pathology and subsequent region-specific neurodegeneration in a cascade similar to amyloid-p peptide in Alzheimer's disease. The key components of the C9orf72 cascade are promising therapeutic targets in different disease stages.
引用
收藏
页码:99 / 106
页数:8
相关论文
共 63 条
[1]   p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS [J].
Al-Sarraj, Safa ;
King, Andrew ;
Troakes, Claire ;
Smith, Bradley ;
Maekawa, Satomi ;
Bodi, Istvan ;
Rogelj, Boris ;
Al-Chalabi, Ammar ;
Hortobagyi, Tibor ;
Shaw, Christopher E. .
ACTA NEUROPATHOLOGICA, 2011, 122 (06) :691-702
[2]   Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons [J].
Almeida, Sandra ;
Gascon, Eduardo ;
Tran, Helene ;
Chou, Hsin Jung ;
Gendron, Tania F. ;
DeGroot, Steven ;
Tapper, Andrew R. ;
Sellier, Chantal ;
Charlet-Berguerand, Nicolas ;
Karydas, Anna ;
Seeley, William W. ;
Boxer, Adam L. ;
Petrucelli, Leonard ;
Miller, Bruce L. ;
Gao, Fen-Biao .
ACTA NEUROPATHOLOGICA, 2013, 126 (03) :385-399
[3]   Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS [J].
Ash, Peter E. A. ;
Bieniek, Kevin F. ;
Gendron, Tania F. ;
Caulfield, Thomas ;
Lin, Wen-Lang ;
DeJesus-Hernandez, Mariely ;
van Blitterswijk, Marka M. ;
Jansen-West, Karen ;
Paul, Joseph W., III ;
Rademakers, Rosa ;
Boylan, Kevin B. ;
Dickson, Dennis W. ;
Petrucelli, Leonard .
NEURON, 2013, 77 (04) :639-646
[4]   Clinical and Biomarker Changes in Dominantly Inherited Alzheimer's Disease [J].
Bateman, Randall J. ;
Xiong, Chengjie ;
Benzinger, Tammie L. S. ;
Fagan, Anne M. ;
Goate, Alison ;
Fox, Nick C. ;
Marcus, Daniel S. ;
Cairns, Nigel J. ;
Xie, Xianyun ;
Blazey, Tyler M. ;
Holtzman, David M. ;
Santacruz, Anna ;
Buckles, Virginia ;
Oliver, Angela ;
Moulder, Krista ;
Aisen, Paul S. ;
Ghetti, Bernardino ;
Klunk, William E. ;
McDade, Eric ;
Martins, Ralph N. ;
Masters, Colin L. ;
Mayeux, Richard ;
Ringman, John M. ;
Rossor, Martin N. ;
Schofield, Peter R. ;
Sperling, Reisa A. ;
Salloway, Stephen ;
Morris, John C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (09) :795-804
[5]   C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits [J].
Chew, Jeannie ;
Gendron, Tania F. ;
Prudencio, Mercedes ;
Sasaguri, Hiroki ;
Zhang, Yong-Jie ;
Castanedes-Casey, Monica ;
Lee, ChrisW. ;
Jansen-West, Karen ;
Kurti, Aishe ;
Murray, Melissa E. ;
Bieniek, Kevin F. ;
Bauer, Peter O. ;
Whitelaw, Ena C. ;
Rousseau, Linda ;
Stankowski, Jeannette N. ;
Stetler, Caroline ;
Daughrity, Lillian M. ;
Perkerson, Emilie A. ;
Desaro, Pamela ;
Johnston, Amelia ;
Overstreet, Karen ;
Edbauer, Dieter ;
Rademakers, Rosa ;
Boylan, Kevin B. ;
Dickson, Dennis W. ;
Fryer, John D. ;
Petrucelli, Leonard .
SCIENCE, 2015, 348 (6239) :1151-1154
[6]   Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy [J].
Cooper-Knock, Johnathan ;
Higginbottom, Adrian ;
Stopford, Matthew J. ;
Highley, J. Robin ;
Ince, Paul G. ;
Wharton, Stephen B. ;
Pickering-Brown, Stuart ;
Kirby, Janine ;
Hautbergue, Guillaume M. ;
Shaw, Pamela J. .
ACTA NEUROPATHOLOGICA, 2015, 130 (01) :63-75
[7]   Sequestration of multiple RNA recognition motif-containing proteins by C9orf72 repeat expansions [J].
Cooper-Knock, Johnathan ;
Walsh, Matthew J. ;
Higginbottom, Adrian ;
Highley, J. Robin ;
Dickman, Mark J. ;
Edbauer, Dieter ;
Ince, Paul G. ;
Wharton, Stephen B. ;
Wilson, Stuart A. ;
Kirby, Janine ;
Hautbergue, Guillaume M. ;
Shaw, Pamela J. .
BRAIN, 2014, 137 :2040-2051
[8]   Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72 [J].
Davidson, Yvonne S. ;
Barker, Holly ;
Robinson, Andrew C. ;
Thompson, Jennifer C. ;
Harris, Jenny ;
Troakes, Claire ;
Smith, Bradley ;
Al-Saraj, Safa ;
Shaw, Chris ;
Rollinson, Sara ;
Masuda-Suzukake, Masami ;
Hasegawa, Masato ;
Pickering-Brown, Stuart ;
Snowden, Julie S. ;
Mann, David M. .
ACTA NEUROPATHOLOGICA COMMUNICATIONS, 2014, 2
[9]   Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS [J].
DeJesus-Hernandez, Mariely ;
Mackenzie, Ian R. ;
Boeve, Bradley F. ;
Boxer, Adam L. ;
Baker, Matt ;
Rutherford, Nicola J. ;
Nicholson, Alexandra M. ;
Finch, NiCole A. ;
Flynn, Heather ;
Adamson, Jennifer ;
Kouri, Naomi ;
Wojtas, Aleksandra ;
Sengdy, Pheth ;
Hsiung, Ging-Yuek R. ;
Karydas, Anna ;
Seeley, William W. ;
Josephs, Keith A. ;
Coppola, Giovanni ;
Geschwind, Daniel H. ;
Wszolek, Zbigniew K. ;
Feldman, Howard ;
Knopman, David S. ;
Petersen, Ronald C. ;
Miller, Bruce L. ;
Dickson, Dennis W. ;
Boylan, Kevin B. ;
Graff-Radford, Neill R. ;
Rademakers, Rosa .
NEURON, 2011, 72 (02) :245-256
[10]   Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viability [J].
Devlin, Anna-Claire ;
Burr, Karen ;
Borooah, Shyamanga ;
Foster, Joshua D. ;
Cleary, Elaine M. ;
Geti, Imbisaat ;
Vallier, Ludovic ;
Shaw, Christopher E. ;
Chandran, Siddharthan ;
Miles, Gareth B. .
NATURE COMMUNICATIONS, 2015, 6