Evidence map›Paper›PMID 33050427›Full record

ArticleJournal of clinical medicine2020

A Novel Bioengineered Functional Motor Unit Platform to Study Neuromuscular Interaction.

Jasdeep Saini, Alessandro Faroni, Adam J Reid, Kamel Mamchaoui, Vincent Mouly, Gillian Butler-Browne, Adam P Lightfoot, Jamie S McPhee, Hans Degens, Nasser Al-Shanti

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  5. Organ on a Chip: A NovelFrontiers in neurology · 2021
    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

10 authors at 3 institutions in 3 countries.

Jasdeep SainiMusculoskeletal Science & Sports Medicine Research Centre, Department of Life Sciences, Manchester Metropolitan University, Manchester M1 5GD, UK.
Alessandro FaroniManchester Academic Health Science Centre, Blond McIndoe Laboratories, Division of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology Medicine and Health, School of Biological Sciences, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0003-4435-6423
Adam J ReidManchester Academic Health Science Centre, Blond McIndoe Laboratories, Division of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology Medicine and Health, School of Biological Sciences, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0003-1752-3302
Kamel MamchaouiCenter for Research in Myology, Sorbonne Université-INSERM, 75013 Paris, France.
Vincent MoulyCenter for Research in Myology, Sorbonne Université-INSERM, 75013 Paris, France.ORCID 0000-0003-3809-4033
Gillian Butler-BrowneCenter for Research in Myology, Sorbonne Université-INSERM, 75013 Paris, France.
Adam P LightfootMusculoskeletal Science & Sports Medicine Research Centre, Department of Life Sciences, Manchester Metropolitan University, Manchester M1 5GD, UK.ORCID 0000-0003-1501-7879
Jamie S McPheeDepartment of Sport and Exercise Sciences, Manchester Metropolitan University, Manchester M1 5GD, UK.ORCID 0000-0002-3659-0773
Hans DegensMusculoskeletal Science & Sports Medicine Research Centre, Department of Life Sciences, Manchester Metropolitan University, Manchester M1 5GD, UK.ORCID 0000-0001-7399-4841
Nasser Al-ShantiMusculoskeletal Science & Sports Medicine Research Centre, Department of Life Sciences, Manchester Metropolitan University, Manchester M1 5GD, UK.
Manchester Metropolitan University · GBInserm · FRManchester Academic Health Science Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn many neurodegenerative and muscular disorders, and loss of innervation in sarcopenia, improper reinnervation of muscle and dysfunction of the motor unit (MU) are key pathogenic features.

objectiveto develop and characterise a functional MU model

methodsan immortalised human myoblast cell line was co-cultured with rat embryo spinal cord explants in a serum-free/growth fact media. MUs developed and the morphology of their components (neuromuscular junction (NMJ), myotubes and motor neurons) were characterised using immunocytochemistry, phase contrast and confocal microscopy. The function of the MU was evaluated through live observations and videography of spontaneous myotube contractions after challenge with cholinergic antagonists and glutamatergic agonists.

resultsblocking acetylcholine receptors with α-bungarotoxin resulted in complete, cessation of myotube contractions, which was reversible with tubocurarine. Furthermore, myotube activity was significantly higher with the application of L-glutamic acid. All these observations indicate the formed MU are functional.

conclusiona functional nerve-muscle co-culture model was established that has potential for drug screening and pathophysiological studies of neuromuscular interactions.

Indexed as

human myoblastmotor neuron (MN) co-culturemotor unit (MU)myotubeneuromuscular junction (NMJ)

Identifiers

PMID33050427
PMCPMC7599749
OpenAlexW3092072927

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.