Literature DB >> 26758825

Electrical and Network Neuronal Properties Are Preferentially Disrupted in Dorsal, But Not Ventral, Medial Entorhinal Cortex in a Mouse Model of Tauopathy.

Clair A Booth1, Thomas Ridler2, Tracey K Murray3, Mark A Ward3, Emily de Groot2, Marc Goodfellow4, Keith G Phillips3, Andrew D Randall5, Jonathan T Brown6.   

Abstract

The entorhinal cortex (EC) is one of the first areas to be disrupted in neurodegenerative diseases such as Alzheimer's disease and frontotemporal dementia. The responsiveness of individual neurons to electrical and environmental stimuli varies along the dorsal-ventral axis of the medial EC (mEC) in a manner that suggests this topographical organization plays a key role in neural encoding of geometric space. We examined the cellular properties of layer II mEC stellate neurons (mEC-SCs) in rTg4510 mice, a rodent model of neurodegeneration. Dorsoventral gradients in certain intrinsic membrane properties, such as membrane capacitance and afterhyperpolarizations, were flattened in rTg4510 mEC-SCs, while other cellular gradients [e.g., input resistance (Ri), action potential properties] remained intact. Specifically, the intrinsic properties of rTg4510 mEC-SCs in dorsal aspects of the mEC were preferentially affected, such that action potential firing patterns in dorsal mEC-SCs were altered, while those in ventral mEC-SCs were unaffected. We also found that neuronal oscillations in the gamma frequency band (30-80 Hz) were preferentially disrupted in the dorsal mEC of rTg4510 slices, while those in ventral regions were comparatively preserved. These alterations corresponded to a flattened dorsoventral gradient in theta-gamma cross-frequency coupling of local field potentials recorded from the mEC of freely moving rTg4510 mice. These differences were not paralleled by changes to the dorsoventral gradient in parvalbumin staining or neurodegeneration. We propose that the selective disruption to dorsal mECs, and the resultant flattening of certain dorsoventral gradients, may contribute to disturbances in spatial information processing observed in this model of dementia. SIGNIFICANCE STATEMENT: The medial entorhinal cortex (mEC) plays a key role in spatial memory and is one of the first areas to express the pathological features of dementia. Neurons of the mEC are anatomically arranged to express functional dorsoventral gradients in a variety of neuronal properties, including grid cell firing field spacing, which is thought to encode geometric scale. We have investigated the effects of tau pathology on functional dorsoventral gradients in the mEC. Using electrophysiological approaches, we have shown that, in a transgenic mouse model of dementia, the functional properties of the dorsal mEC are preferentially disrupted, resulting in a flattening of some dorsoventral gradients. Our data suggest that neural signals arising in the mEC will have a reduced spatial content in dementia.
Copyright © 2016 Booth, Ridler et al.

Entities:  

Keywords:  Tau; dementia; gamma oscillations; grid cells; medial entorhinal cortex

Mesh:

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Year:  2016        PMID: 26758825      PMCID: PMC4710763          DOI: 10.1523/JNEUROSCI.2845-14.2016

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  58 in total

1.  Gamma oscillations induced by kainate receptor activation in the entorhinal cortex in vitro.

Authors:  Mark O Cunningham; Ceri H Davies; Eberhard H Buhl; Nancy Kopell; Miles A Whittington
Journal:  J Neurosci       Date:  2003-10-29       Impact factor: 6.167

2.  Ionic mechanisms in the generation of subthreshold oscillations and action potential clustering in entorhinal layer II stellate neurons.

Authors:  Erik Fransén; Angel A Alonso; Clayton T Dickson; Jacopo Magistretti; Michael E Hasselmo
Journal:  Hippocampus       Date:  2004       Impact factor: 3.899

3.  Spatial representation in the entorhinal cortex.

Authors:  Marianne Fyhn; Sturla Molden; Menno P Witter; Edvard I Moser; May-Britt Moser
Journal:  Science       Date:  2004-08-27       Impact factor: 47.728

4.  A behavioral role for dendritic integration: HCN1 channels constrain spatial memory and plasticity at inputs to distal dendrites of CA1 pyramidal neurons.

Authors:  Matthew F Nolan; Gaël Malleret; Josh T Dudman; Derek L Buhl; Bina Santoro; Emma Gibbs; Svetlana Vronskaya; György Buzsáki; Steven A Siegelbaum; Eric R Kandel; Alexei Morozov
Journal:  Cell       Date:  2004-11-24       Impact factor: 41.582

5.  Activity-dependent decrease of excitability in rat hippocampal neurons through increases in I(h).

Authors:  Yuan Fan; Desdemona Fricker; Darrin H Brager; Xixi Chen; Hui-Chen Lu; Raymond A Chitwood; Daniel Johnston
Journal:  Nat Neurosci       Date:  2005-10-23       Impact factor: 24.884

6.  Microstructure of a spatial map in the entorhinal cortex.

Authors:  Torkel Hafting; Marianne Fyhn; Sturla Molden; May-Britt Moser; Edvard I Moser
Journal:  Nature       Date:  2005-06-19       Impact factor: 49.962

Review 7.  Path integration and the neural basis of the 'cognitive map'.

Authors:  Bruce L McNaughton; Francesco P Battaglia; Ole Jensen; Edvard I Moser; May-Britt Moser
Journal:  Nat Rev Neurosci       Date:  2006-08       Impact factor: 34.870

8.  Age-dependent neurofibrillary tangle formation, neuron loss, and memory impairment in a mouse model of human tauopathy (P301L).

Authors:  Martin Ramsden; Linda Kotilinek; Colleen Forster; Jennifer Paulson; Eileen McGowan; Karen SantaCruz; Aaron Guimaraes; Mei Yue; Jada Lewis; George Carlson; Michael Hutton; Karen H Ashe
Journal:  J Neurosci       Date:  2005-11-16       Impact factor: 6.167

9.  Tau suppression in a neurodegenerative mouse model improves memory function.

Authors:  K Santacruz; J Lewis; T Spires; J Paulson; L Kotilinek; M Ingelsson; A Guimaraes; M DeTure; M Ramsden; E McGowan; C Forster; M Yue; J Orne; C Janus; A Mariash; M Kuskowski; B Hyman; M Hutton; K H Ashe
Journal:  Science       Date:  2005-07-15       Impact factor: 47.728

10.  Region-specific dissociation of neuronal loss and neurofibrillary pathology in a mouse model of tauopathy.

Authors:  Tara L Spires; Jennifer D Orne; Karen SantaCruz; Rose Pitstick; George A Carlson; Karen H Ashe; Bradley T Hyman
Journal:  Am J Pathol       Date:  2006-05       Impact factor: 4.307

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  17 in total

1.  In vitro characterization of cell-level neurophysiological diversity in the rostral nucleus reuniens of adult mice.

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2.  Physiological roles of Kv2 channels in entorhinal cortex layer II stellate cells revealed by Guangxitoxin-1E.

Authors:  Christoph Hönigsperger; Maximiliano J Nigro; Johan F Storm
Journal:  J Physiol       Date:  2016-11-13       Impact factor: 5.182

Review 3.  Gamma oscillations in the entorhinal-hippocampal circuit underlying memory and dementia.

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Journal:  Neurosci Res       Date:  2018-02-10       Impact factor: 3.304

4.  Tau Pathology Induces Excitatory Neuron Loss, Grid Cell Dysfunction, and Spatial Memory Deficits Reminiscent of Early Alzheimer's Disease.

Authors:  Hongjun Fu; Gustavo A Rodriguez; Mathieu Herman; Sheina Emrani; Eden Nahmani; Geoffrey Barrett; Helen Y Figueroa; Eliana Goldberg; S Abid Hussaini; Karen E Duff
Journal:  Neuron       Date:  2017-01-19       Impact factor: 17.173

5.  β Bursting in the Retrosplenial Cortex Is a Neurophysiological Correlate of Environmental Novelty Which Is Disrupted in a Mouse Model of Alzheimer's Disease.

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Journal:  J Neurosci       Date:  2022-08-04       Impact factor: 6.709

6.  Initiation and slow propagation of epileptiform activity from ventral to dorsal medial entorhinal cortex is constrained by an inhibitory gradient.

Authors:  Thomas Ridler; Peter Matthews; Keith G Phillips; Andrew D Randall; Jonathan T Brown
Journal:  J Physiol       Date:  2018-04-25       Impact factor: 5.182

7.  Early Cortical Changes in Gamma Oscillations in Alzheimer's Disease.

Authors:  Alexandra S Klein; José R Donoso; Richard Kempter; Dietmar Schmitz; Prateep Beed
Journal:  Front Syst Neurosci       Date:  2016-10-26

8.  Control of clustered action potential firing in a mathematical model of entorhinal cortex stellate cells.

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9.  Early Electrophysiological Disintegration of Hippocampal Neural Networks in a Novel Locus Coeruleus Tau-Seeding Mouse Model of Alzheimer's Disease.

Authors:  A Ahnaou; C Walsh; N V Manyakov; S A Youssef; W H Drinkenburg
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10.  Hippocampal neurophysiology is modified by a disease-associated C-terminal fragment of tau protein.

Authors:  Francesco Tamagnini; Darren A Walsh; Jon T Brown; Marie K Bondulich; Diane P Hanger; Andrew D Randall
Journal:  Neurobiol Aging       Date:  2017-07-20       Impact factor: 4.673

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