Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2016Altered intrinsic pyramidal neuron properties and pathway- specific synaptic dysfunction underlie aberrant hippocampal network function in a mouse model of tauopathy92citations

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Chart of shared publication
Jones, Matthew
1 / 1 shared
Brown, Jon T.
1 / 1 shared
Randall, Andy D.
1 / 1 shared
Tsaneva-Atanasova, Krasimira
1 / 2 shared
Booth, Clair A.
1 / 1 shared
Witton, Jonathan
1 / 1 shared
Chart of publication period
2016

Co-Authors (by relevance)

  • Jones, Matthew
  • Brown, Jon T.
  • Randall, Andy D.
  • Tsaneva-Atanasova, Krasimira
  • Booth, Clair A.
  • Witton, Jonathan
OrganizationsLocationPeople

article

Altered intrinsic pyramidal neuron properties and pathway- specific synaptic dysfunction underlie aberrant hippocampal network function in a mouse model of tauopathy

  • Jones, Matthew
  • Brown, Jon T.
  • Randall, Andy D.
  • Nowacki, Jakub
  • Tsaneva-Atanasova, Krasimira
  • Booth, Clair A.
  • Witton, Jonathan
Abstract

<p>The formation and deposition of tau protein aggregates is proposed to contribute to cognitive impairments in dementia by disrupting neuronal function in brain regions, including the hippocampus. We used a battery of <em>in vivo</em> and <em>in vitro</em> electrophysiological recordings in the rTg4510 transgenic mouse model, which overexpresses a mutant form of human tau protein, to investigate the effects of tau pathology on hippocampal neuronal function in area CA1 of 7- to 8-month-old mice, an age point at which rTg4510 animals exhibit advanced tau pathology and progressive neurodegeneration. <em>In vitro</em> recordings revealed shifted theta-frequency resonance properties of CA1 pyramidal neurons, deficits in synaptic transmission at Schaffer collateral synapses, and blunted plasticity and imbalanced inhibition at temporoammonic synapses. These changes were associated with aberrant CA1 network oscillations, pyramidal neuron bursting, and spatial information coding <em>in vivo</em>. Our findings relate tauopathy-associated changes in cellular neurophysiology to altered behavior-dependent network function.</p><p><strong>SIGNIFICANCE STATEMENT</strong> Dementia is characterized by the loss of learning and memory ability. The deposition of tau protein aggregates in the brain is a pathological hallmark of dementia; and the hippocampus, a brain structure known to be critical in processing learning and memory, is one of the first and most heavily affected regions. Our results show that, in area CA1 of hippocampus, a region involved in spatial learning and memory, tau pathology is associated with specific disturbances in synaptic, cellular, and network-level function, culminating in the aberrant encoding of spatial information and spatial memory impairment. These studies identify several novel ways in which hippocampal information processing may be disrupted in dementia, which may provide targets for future therapeutic intervention.</p>

Topics
  • Deposition
  • impedance spectroscopy
  • plasticity