A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration

被引:221
作者
Walsh, Dominic M. [1 ]
Selkoe, Dennis J. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Ann Romney Ctr Neurol Dis,Dept Neurol, Boston, MA 02115 USA
关键词
CREUTZFELDT-JAKOB-DISEASE; CEREBRAL BETA-AMYLOIDOSIS; CELLULAR PRION PROTEIN; TAU TRANSGENIC MICE; PARKINSONS-DISEASE; ALZHEIMERS-DISEASE; ALPHA-SYNUCLEIN; CEREBROSPINAL-FLUID; SPONGIFORM ENCEPHALOPATHY; LONG-TERM;
D O I
10.1038/nrn.2016.13
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
There has been an explosion in the number of papers discussing the hypothesis of 'pathogenic spread' in neurodegenerative disease - the idea that abnormal forms of disease-associated proteins, such as tau or a-synuclein, physically move from neuron to neuron to induce disease progression. However, whether inter-neuronal spread of protein aggregates actually occurs in humans and, if so, whether it causes symptom onset remain uncertain. Even if pathogenic spread is proven in humans, it is unclear how much this would alter the specific therapeutic approaches that are in development. A critical appraisal of this increasingly popular hypothesis thus seems both important and timely.
引用
收藏
页码:251 / 260
页数:10
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