Evidence map›Paper›PMID 24763087›Full record

ArticlePLoS computational biology2014

Glutamate-bound NMDARs arising from in vivo-like network activity extend spatio-temporal integration in a L5 cortical pyramidal cell model.

Matteo Farinella, Daniel T Ruedt, Padraig Gleeson, Frederic Lanore, R Angus Silver

Abstract read
In one paragraph

Article in PLoS computational biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Article
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  9. Review
  10. Active dendrites enable strong but sparse inputs to determine orientation selectivity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Article
  12. Review
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  18. Cell-type-specific inhibition of the dendritic plateau potential in striatal spiny projection neurons.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  19. Article
  20. Dendritic Spikes in Sensory Perception.Frontiers in cellular neuroscience · 2017
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Matteo FarinellaDepartment of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom.
Daniel T RuedtDepartment of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom.
Padraig GleesonDepartment of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom.
Frederic LanoreDepartment of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom.
R Angus SilverDepartment of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom.

Funding

Wellcome TrustWellcome Trust 086699Wellcome Trust 095667Wellcome Trust 101445
6 · The paper itself

Abstract

In vivo, cortical pyramidal cells are bombarded by asynchronous synaptic input arising from ongoing network activity. However, little is known about how such 'background' synaptic input interacts with nonlinear dendritic mechanisms. We have modified an existing model of a layer 5 (L5) pyramidal cell to explore how dendritic integration in the apical dendritic tuft could be altered by the levels of network activity observed in vivo. Here we show that asynchronous background excitatory input increases neuronal gain and extends both temporal and spatial integration of stimulus-evoked synaptic input onto the dendritic tuft. Addition of fast and slow inhibitory synaptic conductances, with properties similar to those from dendritic targeting interneurons, that provided a 'balanced' background configuration, partially counteracted these effects, suggesting that inhibition can tune spatio-temporal integration in the tuft. Excitatory background input lowered the threshold for NMDA receptor-mediated dendritic spikes, extended their duration and increased the probability of additional regenerative events occurring in neighbouring branches. These effects were also observed in a passive model where all the non-synaptic voltage-gated conductances were removed. Our results show that glutamate-bound NMDA receptors arising from ongoing network activity can provide a powerful spatially distributed nonlinear dendritic conductance. This may enable L5 pyramidal cells to change their integrative properties as a function of local network activity, potentially allowing both clustered and spatially distributed synaptic inputs to be integrated over extended timescales.

Indexed as

Models, BiologicalCerebral CortexDendritesGlutamic AcidPyramidal CellsReceptors, N-Methyl-D-AspartateSynapsesGlutamic AcidReceptors, N-Methyl-D-Aspartate

Identifiers

PMID24763087
PMCPMC3998913

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.