Alzheimer brain-derived tau oligomers propagate pathology from endogenous tau

被引:379
作者
Lasagna-Reeves, Cristian A. [1 ,2 ]
Castillo-Carranza, Diana L. [1 ,2 ]
Sengupta, Urmi [1 ,2 ]
Guerrero-Munoz, Marcos J. [1 ,2 ]
Kiritoshi, Takaki
Neugebauer, Volker
Jackson, George R. [1 ,2 ]
Kayed, Rakez [1 ,2 ]
机构
[1] Univ Texas Med Branch, George P & Cynthia Woods Mitchell Ctr Neurodegene, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Neurol, Galveston, TX 77555 USA
关键词
NUCLEATED CONFORMATIONAL CONVERSION; INDUCED DEFECTS; PROTEIN; MEMORY; MODEL; PRIONS; GROWTH; NEURODEGENERATION; TRANSMISSION; MECHANISMS;
D O I
10.1038/srep00700
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intracerebral injection of brain extracts containing amyloid or tau aggregates in transgenic animals can induce cerebral amyloidosis and tau pathology. We extracted pure populations of tau oligomers directly from the cerebral cortex of Alzheimer disease (AD) brain. These oligomers are potent inhibitors of long term potentiation (LTP) in hippocampal brain slices and disrupt memory in wild type mice. We observed for the first time that these authentic brain-derived tau oligomers propagate abnormal tau conformation of endogenous murine tau after prolonged incubation. The conformation and hydrophobicity of tau oligomers play a critical role in the initiation and spread of tau pathology in the naive host in a manner reminiscent of sporadic AD.
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页数:7
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