Cerebrospinal fluid from Alzheimer's disease patients promotes tau aggregation in transgenic mice

被引:20
作者
Skachokova, Zhiva [1 ,2 ]
Martinisi, Alfonso [1 ,2 ]
Flach, Martin [1 ,2 ]
Sprenger, Frederik [1 ,2 ]
Naegelin, Yvonne [2 ]
Steiner-Monard, Viviane [3 ,4 ]
Sollberger, Marc [2 ,3 ,4 ]
Monsch, Andreas U. [3 ,4 ]
Goedert, Michel [5 ]
Tolnay, Markus [1 ]
Winkler, David T. [1 ,2 ,6 ]
机构
[1] Univ Hosp Basel, Inst Med Genet & Pathol, Petersgraben 4, CH-4031 Basel, Switzerland
[2] Univ Hosp Basel, Dept Neurol, Petersgraben 4, CH-4031 Basel, Switzerland
[3] Felix Platter Hosp, Univ Ctr Med Aging, Memory Clin, Burgfelderstr 101, CH-4002 Basel, Switzerland
[4] Univ Basel, Burgfelderstr 101, CH-4002 Basel, Switzerland
[5] MRC, Mol Biol Lab, Francis Crick Ave, Cambridge CB2 0QH, England
[6] Kantonsspital Baselland, Med Univ Clin, Neurol, Rheinstr 26, CH-4410 Liestal, Switzerland
基金
英国医学研究理事会; 瑞士国家科学基金会;
关键词
Alzheimer's disease; Neurodegeneration; Tau; Cerebrospinal fluid; Seeding; Prion; Transgenic mouse models; NEUROFIBRILLARY CHANGES; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; PATHOLOGICAL TAU; SEEDING ACTIVITY; AMYLOID-BETA; RECOMMENDATIONS; PROPAGATION; SPREAD;
D O I
10.1186/s40478-019-0725-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tau is a microtubule stabilizing protein that forms aggregates in Alzheimer's disease (AD). Tau derived from AD patients' brains induces tau aggregation in a prion-like manner when injected into susceptible mouse models.Here we investigated whether cerebrospinal fluid (CSF) collected from patients diagnosed with probable AD or mild cognitive impairment (MCI) likely due to AD harbors a prion-like tau seeding potential. CSF was injected intrahippocampally into young P301S tau transgenic mice. CSF obtained from AD or MCI patients increased hippocampal tau hyperphosphorylation and tau tangle formation in these mice at 4months post-seeding. Tau pathology was also accentuated in the contralateral hippocampus, and in anterior and posterior directions, indicative of spreading.We provide first evidence for in vivo prion-like properties of AD patients' CSF, accelerating tau pathology in susceptible tau transgenic mice. This demonstrates that biologically active tau seeds reach the CSF compartment in AD. Further studies may help to evaluate strain specific properties of CSF derived tau bioseeds, and to assess their diagnostic potential.
引用
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页数:9
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