Evidence map›Paper›PMID 27147977›Full record

ArticleFrontiers in neural circuits2016

Feed-Forward Propagation of Temporal and Rate Information between Cortical Populations during Coherent Activation in Engineered In Vitro Networks.

Thomas B DeMarse, Liangbin Pan, Sankaraleengam Alagapan, Gregory J Brewer, Bruce C Wheeler

Abstract read
In one paragraph

Article in Frontiers in neural circuits, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Coupling ofFrontiers in neuroscience · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Neural Circuits on a Chip.Micromachines · 2016
    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.

Thomas B DeMarseJ. Crayton Pruitt Family Department of Biomedical Engineering, University of FloridaGainesville, FL, USA; Department of Pediatric Neurology, University of FloridaGainesville, FL, USA.
Liangbin PanJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida Gainesville, FL, USA.
Sankaraleengam AlagapanJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida Gainesville, FL, USA.
Gregory J BrewerDepartment of Bioengineering, University of California Irvine, CA, USA.
Bruce C WheelerJ. Crayton Pruitt Family Department of Biomedical Engineering, University of FloridaGainesville, FL, USA; Department of Bioengineering, University of CaliforniaSan Diego, CA, USA.

Funding

ENGINEERING FORM AND FUNCTION IN NEURONAL NETWORKSR01NS052233 · NINDS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI WHEELER, BRUCE C. · 2006 to 2016
$4.1M
NINDS NIH HHS NS052233NINDS NIH HHS R01 NS052233
6 · The paper itself

Abstract

Transient propagation of information across neuronal assembles is thought to underlie many cognitive processes. However, the nature of the neural code that is embedded within these transmissions remains uncertain. Much of our understanding of how information is transmitted among these assemblies has been derived from computational models. While these models have been instrumental in understanding these processes they often make simplifying assumptions about the biophysical properties of neurons that may influence the nature and properties expressed. To address this issue we created an in vitro analog of a feed-forward network composed of two small populations (also referred to as assemblies or layers) of living dissociated rat cortical neurons. The populations were separated by, and communicated through, a microelectromechanical systems (MEMS) device containing a strip of microscale tunnels. Delayed culturing of one population in the first layer followed by the second a few days later induced the unidirectional growth of axons through the microtunnels resulting in a primarily feed-forward communication between these two small neural populations. In this study we systematically manipulated the number of tunnels that connected each layer and hence, the number of axons providing communication between those populations. We then assess the effect of reducing the number of tunnels has upon the properties of between-layer communication capacity and fidelity of neural transmission among spike trains transmitted across and within layers. We show evidence based on Victor-Purpura's and van Rossum's spike train similarity metrics supporting the presence of both rate and temporal information embedded within these transmissions whose fidelity increased during communication both between and within layers when the number of tunnels are increased. We also provide evidence reinforcing the role of synchronized activity upon transmission fidelity during the spontaneous synchronized network burst events that propagated between layers and highlight the potential applications of these MEMs devices as a tool for further investigation of structure and functional dynamics among neural populations.

Indexed as

Models, NeurologicalAction PotentialsAnalysis of VarianceAnimalsBiophysical PhenomenaBiophysicsCells, CulturedCerebral CortexElectric StimulationEmbryo, MammalianIn Vitro TechniquesNerve NetNeuronsPatch-Clamp TechniquesPrincipal Component AnalysisRatscortical networksfeed-forward networksinformation transmissionmultielectrode arrayneural populationsneural transmissionneuronal assemblysynchrony

Identifiers

PMID27147977
PMCPMC4840215

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.