Mutant Tau knock-in mice display frontotemporal dementia relevant behaviour and histopathology

David J. Koss, Lianne Robinson, Benjamin D. Drever, Kaja Plucinska, Sandra Stoppelkamp, Peter Veselcic, Gernot Riedel, Bettina Platt (Corresponding Author)

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Abstract

Models of Tau pathology related to frontotemporal dementia (FTD) are essential to determine underlying neurodegenerative pathologies and resulting tauopathy relevant behavioural changes. However, existing models are often limited in their translational value due to Tau overexpression, and the frequent occurrence of motor deficits which prevent comprehensive behavioural assessments. In order to address these limitations, a forebrain-specific (CaMKIIα promoter), human mutated Tau (hTauP301L + R406W) knock-in mouse was generated out of the previously characterised PLB1Triple mouse, and named PLB2Tau. After confirmation of an additional hTau species (~ 60 kDa) in forebrain samples, we identified age-dependent progressive Tau phosphorylation which coincided with the emergence of FTD relevant behavioural traits. In line with the non-cognitive symptomatology of FTD, PLB2Tau mice demonstrated early emerging (~ 6 months) phenotypes of heightened anxiety in the elevated plus maze, depressive/apathetic behaviour in a sucrose preference test and generally reduced exploratory activity in the absence of motor impairments. Investigations of cognitive performance indicated prominent dysfunctions in semantic memory, as assessed by social transmission of food preference, and in behavioural flexibility during spatial reversal learning in a home cage corner-learning task. Spatial learning was only mildly affected and task-specific, with impairments at 12 months of age in the corner learning but not in the water maze task. Electroencephalographic (EEG) investigations indicated a vigilance-stage specific loss of alpha power during wakefulness at both parietal and prefrontal recording sites, and site-specific EEG changes during non-rapid eye movement sleep (prefrontal) and rapid eye movement sleep (parietal). Further investigation of hippocampal electrophysiology conducted in slice preparations indicated a modest reduction in efficacy of synaptic transmission in the absence of altered synaptic plasticity.

Together, our data demonstrate that the transgenic PLB2Tau mouse model presents with a striking behavioural and physiological face validity relevant for FTD, driven by the low level expression of mutant FTD hTau.
Original languageEnglish
Pages (from-to)105-123
Number of pages19
JournalNeurobiology of Disease
Volume91
Early online date4 Mar 2016
DOIs
Publication statusPublished - Jul 2016

Fingerprint

Frontotemporal Dementia
Prosencephalon
Sleep
Learning
Reversal Learning
Tauopathies
Pathology
Food Preferences
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Neuronal Plasticity
Wakefulness
Electrophysiology
REM Sleep
Eye Movements
Semantics
Reproducibility of Results
Synaptic Transmission
Transgenic Mice
Sucrose
Anxiety

Keywords

  • frontotemporal dementia
  • tauopathies
  • tau
  • phosphorylation
  • cognition
  • apathy
  • anhedonia
  • semantic memory
  • spatial memory
  • EEG

Cite this

Mutant Tau knock-in mice display frontotemporal dementia relevant behaviour and histopathology. / Koss, David J.; Robinson, Lianne; Drever, Benjamin D.; Plucinska, Kaja; Stoppelkamp, Sandra; Veselcic, Peter; Riedel, Gernot; Platt, Bettina (Corresponding Author).

In: Neurobiology of Disease, Vol. 91, 07.2016, p. 105-123.

Research output: Contribution to journalArticle

Koss, David J. ; Robinson, Lianne ; Drever, Benjamin D. ; Plucinska, Kaja ; Stoppelkamp, Sandra ; Veselcic, Peter ; Riedel, Gernot ; Platt, Bettina. / Mutant Tau knock-in mice display frontotemporal dementia relevant behaviour and histopathology. In: Neurobiology of Disease. 2016 ; Vol. 91. pp. 105-123.
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AB - Models of Tau pathology related to frontotemporal dementia (FTD) are essential to determine underlying neurodegenerative pathologies and resulting tauopathy relevant behavioural changes. However, existing models are often limited in their translational value due to Tau overexpression, and the frequent occurrence of motor deficits which prevent comprehensive behavioural assessments. In order to address these limitations, a forebrain-specific (CaMKIIα promoter), human mutated Tau (hTauP301L + R406W) knock-in mouse was generated out of the previously characterised PLB1Triple mouse, and named PLB2Tau. After confirmation of an additional hTau species (~ 60 kDa) in forebrain samples, we identified age-dependent progressive Tau phosphorylation which coincided with the emergence of FTD relevant behavioural traits. In line with the non-cognitive symptomatology of FTD, PLB2Tau mice demonstrated early emerging (~ 6 months) phenotypes of heightened anxiety in the elevated plus maze, depressive/apathetic behaviour in a sucrose preference test and generally reduced exploratory activity in the absence of motor impairments. Investigations of cognitive performance indicated prominent dysfunctions in semantic memory, as assessed by social transmission of food preference, and in behavioural flexibility during spatial reversal learning in a home cage corner-learning task. Spatial learning was only mildly affected and task-specific, with impairments at 12 months of age in the corner learning but not in the water maze task. Electroencephalographic (EEG) investigations indicated a vigilance-stage specific loss of alpha power during wakefulness at both parietal and prefrontal recording sites, and site-specific EEG changes during non-rapid eye movement sleep (prefrontal) and rapid eye movement sleep (parietal). Further investigation of hippocampal electrophysiology conducted in slice preparations indicated a modest reduction in efficacy of synaptic transmission in the absence of altered synaptic plasticity.Together, our data demonstrate that the transgenic PLB2Tau mouse model presents with a striking behavioural and physiological face validity relevant for FTD, driven by the low level expression of mutant FTD hTau.

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