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024 7 _ |a 10.1016/j.neurobiolaging.2012.10.024
|2 doi
024 7 _ |a pmid:23158765
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024 7 _ |a pmc:PMC4984976
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024 7 _ |a 0197-4580
|2 ISSN
024 7 _ |a 1558-1497
|2 ISSN
037 _ _ |a DZNE-2020-03149
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Messing, Lars
|0 P:(DE-2719)2810335
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|e First author
|u dzne
245 _ _ |a Cascade of tau toxicity in inducible hippocampal brain slices and prevention by aggregation inhibitors.
260 _ _ |a Amsterdam [u.a.]
|c 2013
|b Elsevier Science
264 _ 1 |3 print
|2 Crossref
|b Elsevier BV
|c 2013-05-01
336 7 _ |a article
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
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520 _ _ |a Mislocalization and aggregation of the axonal protein tau are hallmarks of Alzheimer's disease and other tauopathies. Here, we studied the relationship between tau aggregation, loss of spines and neurons, and reversibility by aggregation inhibitors. To this end we established an in vitro model of tauopathy based on regulatable transgenic hippocampal organotypic slice cultures prepared from mice expressing proaggregant Tau repeat domain with mutation ΔK280 (Tau(RD)ΔK). Transgene expression was monitored by a bioluminescence reporter assay. We observed abnormal tau phosphorylation and mislocalization of exogenous and endogenous tau into the somatodendritic compartment. This was paralleled by a reduction of dendritic spines, altered dendritic spine morphology, dysregulation of Ca(++) dynamics and elevated activation of microglia. Neurotoxicity was mediated by Caspase-3 activation and correlated with the expression level of proaggregant Tau(RD)ΔK. Finally, tau aggregates appeared in areas CA1 and CA3 after three weeks in vitro. Neurodegeneration was relieved by aggregation inhibitors or by switching off transgene expression. Thus the slice culture model is suitable for monitoring the development of tauopathy and the therapeutic benefit of antiaggregation drugs.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
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542 _ _ |i 2013-05-01
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650 _ 7 |a Mapt protein, mouse
|2 NLM Chemicals
650 _ 7 |a tau Proteins
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Calcium Signaling
|2 MeSH
650 _ 2 |a Cells, Cultured
|2 MeSH
650 _ 2 |a Dimerization
|2 MeSH
650 _ 2 |a Hippocampus: pathology
|2 MeSH
650 _ 2 |a Hippocampus: physiopathology
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Mice, Transgenic
|2 MeSH
650 _ 2 |a Neurons: pathology
|2 MeSH
650 _ 2 |a Tauopathies: physiopathology
|2 MeSH
650 _ 2 |a tau Proteins: metabolism
|2 MeSH
700 1 _ |a Decker, Jochen Martin
|0 P:(DE-2719)2810343
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700 1 _ |a Joseph, Maria
|0 P:(DE-2719)2813357
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700 1 _ |a Mandelkow, Eckhard
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700 1 _ |a Mandelkow, Eva-Maria
|0 P:(DE-2719)2541658
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773 1 8 |a 10.1016/j.neurobiolaging.2012.10.024
|b : Elsevier BV, 2013-05-01
|n 5
|p 1343-1354
|3 journal-article
|2 Crossref
|t Neurobiology of Aging
|v 34
|y 2013
|x 0197-4580
773 _ _ |a 10.1016/j.neurobiolaging.2012.10.024
|g Vol. 34, no. 5, p. 1343 - 1354
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856 7 _ |2 Pubmed Central
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856 4 _ |u https://pub.dzne.de/record/136827/files/DZNE-2020-03149_Restricted.pdf
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