Synthetic Tau Fibrils Mediate Transmission of Neurofibrillary Tangles in a Transgenic Mouse Model of Alzheimer's-Like Tauopathy

被引:507
作者
Iba, Michiyo [1 ]
Guo, Jing L. [1 ]
McBride, Jennifer D. [1 ]
Zhang, Bin [1 ]
Trojanowski, John Q. [1 ]
Lee, Virginia M-Y [1 ]
机构
[1] Univ Penn, Sch Med, Dept Pathol & Lab, Ctr Neurodegenerat Dis Res,Inst Aging, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
FIBRILLIZATION IN-VITRO; LOCUS-COERULEUS; PROTEIN-TAU; DISEASE; PATHOLOGY; BRAIN; PROPAGATION; DEMENTIA; NEURODEGENERATION; AGGREGATION;
D O I
10.1523/JNEUROSCI.2642-12.2013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tauopathies, including Alzheimer's disease (AD) and frontotemporal lobar degeneration with tau pathologies, are neurodegenerative diseases characterized by neurofibrillary tangles (NFTs) comprising filamentous tau protein. Although emerging evidence suggests that tau pathology may be transmitted, we demonstrate here that synthetic tau fibrils are sufficient to transmit tau inclusions in a mouse model. Specifically, intracerebral inoculation of young PS19 mice overexpressing mutant human tau (P301S) with synthetic preformed fibrils (pffs) assembled from recombinant full-length tau or truncated tau containing four microtubule binding repeats resulted in rapid induction of NFT-like inclusions that propagated from injected sites to connected brain regions in a time-dependent manner. Interestingly, injection of tau pffs into either hippocampus or striatum together with overlaying cortex gave rise to distinct pattern of spreading. Moreover, unlike tau pathology that spontaneously develops in old PS19 mice, the pff-induced tau inclusions more closely resembled AD NFTs because they were Thioflavin S positive, acetylated, and more resistant to proteinase K digestion. Together, our study demonstrates that synthetic tau pffs alone are capable of inducing authentic NFT-like tau aggregates and initiating spreading of tau pathology in a tauopathy mouse model.
引用
收藏
页码:1024 / 1037
页数:14
相关论文
共 44 条
[1]   An integrative theory of locus coeruleus-norepinephrine function: Adaptive gain and optimal performance [J].
Aston-Jones, G ;
Cohen, JD .
ANNUAL REVIEW OF NEUROSCIENCE, 2005, 28 :403-450
[2]   THE BRAIN NUCLEUS LOCUS-COERULEUS - RESTRICTED AFFERENT CONTROL OF A BROAD EFFERENT NETWORK [J].
ASTONJONES, G ;
ENNIS, M ;
PIERIBONE, VA ;
NICKELL, WT ;
SHIPLEY, MT .
SCIENCE, 1986, 234 (4777) :734-737
[3]   Tau-mediated neurodegeneration in Alzheimer's disease and related disorders [J].
Ballatore, Carlo ;
Lee, Virginia M. -Y. ;
Trojanowski, John Q. .
NATURE REVIEWS NEUROSCIENCE, 2007, 8 (09) :663-672
[4]   The locus coeruleus-noradrenergic system: modulation of behavioral state and state-dependent cognitive processes [J].
Berridge, CW ;
Waterhouse, BD .
BRAIN RESEARCH REVIEWS, 2003, 42 (01) :33-84
[5]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[6]   Alzheimer's pathogenesis: is there neuron-to-neuron propagation? [J].
Braak, Heiko ;
Del Tredici, Kelly .
ACTA NEUROPATHOLOGICA, 2011, 121 (05) :589-595
[7]   The pathological process underlying Alzheimer's disease in individuals under thirty [J].
Braak, Heiko ;
Del Tredici, Kelly .
ACTA NEUROPATHOLOGICA, 2011, 121 (02) :171-181
[8]   Chronic Stress Exacerbates Tau Pathology, Neurodegeneration, and Cognitive Performance through a Corticotropin-Releasing Factor Receptor-Dependent Mechanism in a Transgenic Mouse Model of Tauopathy [J].
Carroll, Jenna C. ;
Iba, Michiyo ;
Bangasser, Debra A. ;
Valentino, Rita J. ;
James, Michael J. ;
Brunden, Kurt R. ;
Lee, Virginia M-Y ;
Trojanowski, John Q. .
JOURNAL OF NEUROSCIENCE, 2011, 31 (40) :14436-14449
[9]  
CHANPALAY V, 1991, PROG BRAIN RES, V88, P625
[10]   Anionic micelles and vesicles induce tau fibrillization in vitro [J].
Chirita, CN ;
Necula, M ;
Kuret, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (28) :25644-25650