Evidence map›Paper›PMID 29142321›Full record

ArticleScientific reports2017

Design of Cultured Neuron Networks in vitro with Predefined Connectivity Using Asymmetric Microfluidic Channels.

Arseniy Gladkov, Yana Pigareva, Daria Kutyina, Vladimir Kolpakov, Anton Bukatin, Irina Mukhina, Victor Kazantsev, Alexey Pimashkin

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

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  13. Beyond a Transmission Cable-New Technologies to Reveal the Richness in Axonal Electrophysiology.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
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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

8 authors.

Arseniy GladkovLobachevsky State University of Nizhny Novgorod, Laboratory of Neuroengineering, Nizhny Novgorod, 603950, Russia. gladkov@neuro.nnov.ru.ORCID 0000-0002-1831-808X
Yana PigarevaLobachevsky State University of Nizhny Novgorod, Laboratory of Neuroengineering, Nizhny Novgorod, 603950, Russia.
Daria KutyinaLobachevsky State University of Nizhny Novgorod, Laboratory of Neuroengineering, Nizhny Novgorod, 603950, Russia.
Vladimir KolpakovLobachevsky State University of Nizhny Novgorod, Laboratory of Neuroengineering, Nizhny Novgorod, 603950, Russia.
Anton BukatinSaint-Petersburg National Research Academic University of the RAS, Laboratory of Nanobiotechnology, Saint-Petersburg, 194021, Russia.
Irina MukhinaLobachevsky State University of Nizhny Novgorod, Laboratory of Neuroengineering, Nizhny Novgorod, 603950, Russia.
Victor KazantsevLobachevsky State University of Nizhny Novgorod, Laboratory of Neuroengineering, Nizhny Novgorod, 603950, Russia.
Alexey PimashkinLobachevsky State University of Nizhny Novgorod, Laboratory of Neuroengineering, Nizhny Novgorod, 603950, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The architecture of neuron connectivity in brain networks is one of the basic mechanisms by which to organize and sustain a particular function of the brain circuitry. There are areas of the brain composed of well-organized layers of neurons connected by unidirectional synaptic connections (e.g., cortex, hippocampus). Re-engineering of the neural circuits with such a heterogeneous network structure in culture may uncover basic mechanisms of emergent information functions of these circuits. In this study, we present such a model designed with two subpopulations of primary hippocampal neurons (E18) with directed connectivity grown in a microfluidic device with asymmetric channels. We analysed and compared neurite growth in the microchannels with various shapes that promoted growth dominantly in one direction. We found an optimal geometric shape features of the microchannels in which the axons coupled two chambers with the neurons. The axons grew in the promoted direction and formed predefined connections during the first 6 days in vitro (DIV). The microfluidic devices were coupled with microelectrode arrays (MEAs) to confirm unidirectional spiking pattern propagation through the microchannels between two compartments. We found that, during culture development, the defined morphological and functional connectivity formed and was maintained for up to 25 DIV.

Identifiers

PMID29142321
PMCPMC5688062

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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.