Evidence map›Paper›PMID 30341335›Full record

ArticleScientific reports2018

A closer look at neuron interaction with track-etched microporous membranes.

Julian H George, David Nagel, Sharlayne Waller, Eric Hill, H Rhein Parri, Michael D Coleman, Zhanfeng Cui, Hua Ye

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
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

8 citing papers in PubMed, 27 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Julian H GeorgeInstitute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, OX3 7DQ, UK.ORCID http://orcid.org/0000-0002-0701-5040
David NagelAston Research Centre for Healthy Ageing, Life and Health Sciences, Aston University, Birmingham, B4 7ET, UK.ORCID http://orcid.org/0000-0002-9055-1775
Sharlayne WallerInstitute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, OX3 7DQ, UK.ORCID http://orcid.org/0000-0001-8581-6022
Eric HillAston Research Centre for Healthy Ageing, Life and Health Sciences, Aston University, Birmingham, B4 7ET, UK.ORCID http://orcid.org/0000-0002-9419-1500
H Rhein ParriAston Research Centre for Healthy Ageing, Life and Health Sciences, Aston University, Birmingham, B4 7ET, UK.ORCID http://orcid.org/0000-0002-1412-2688
Michael D ColemanAston Research Centre for Healthy Ageing, Life and Health Sciences, Aston University, Birmingham, B4 7ET, UK.ORCID http://orcid.org/0000-0002-5510-6852
Zhanfeng CuiInstitute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, OX3 7DQ, UK.ORCID http://orcid.org/0000-0002-9251-9752
Hua YeInstitute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, OX3 7DQ, UK. hua.ye@eng.ox.ac.uk.ORCID http://orcid.org/0000-0001-7613-6041
Aston University · GBUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H008527/1Biotechnology and Biological Sciences Research Council BB/H008608/1Biotechnology and Biological Sciences Research Council (BBSRC) BB/H008527/1
6 · The paper itself

Abstract

Microporous membranes support the growth of neurites into and through micro-channels, providing a different type of neural growth platform to conventional dish cultures. Microporous membranes are used to support various types of culture, however, the role of pore diameter in relation to neurite growth through the membrane has not been well characterised. In this study, the human cell line (SH-SY5Y) was differentiated into neuron-like cells and cultured on track-etched microporous membranes with pore and channel diameters selected to accommodate neurite width (0.8 µm to 5 µm). Whilst neurites extended through all pore diameters, the extent of neurite coverage on the non-seeded side of the membranes after 5 days in culture was found to be directly proportional to channel diameter. Neurite growth through membrane pores reduced significantly when neural cultures were non-confluent. Scanning electron microscopy revealed that neurites bridged pores and circumnavigated pore edges - such that the overall likelihood of a neurite entering a pore channel was decreased. These findings highlight the role of pore diameter, cell sheet confluence and contact guidance in directing neurite growth through pores and may be useful in applications that seek to use physical substrates to maintain separate neural populations whilst permitting neurite contact between cultures.

Indexed as

Cell ProliferationMembranesCell Culture TechniquesCell LineHumansMicroscopy, Electron, ScanningNeurites

Identifiers

PMID30341335
PMCPMC6195627
OpenAlexW2896267180

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.