Evidence map›Paper›PMID 28637511›Full record

ArticleNeural development2017

The emergence of mesencephalic trigeminal neurons.

Marcela Lipovsek, Julia Ledderose, Thomas Butts, Tanguy Lafont, Clemens Kiecker, Andrea Wizenmann, Anthony Graham

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

9 citing papers in PubMed, 15 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

7 authors at 4 institutions in 2 countries.

Marcela LipovsekCentre for Developmental Neurobiology, Kings College London, London, SE1 1UL, UK.
Julia LedderoseInstitute of Clinical Anatomy and Cell Analysis, Department of Anatomy, University of Tübingen, Oesterbergstrasse 3, 72074, Tuebingen, Germany.
Thomas ButtsCentre for Developmental Neurobiology, Kings College London, London, SE1 1UL, UK.
Tanguy LafontCentre for Developmental Neurobiology, Kings College London, London, SE1 1UL, UK.
Clemens KieckerCentre for Developmental Neurobiology, Kings College London, London, SE1 1UL, UK.
Andrea WizenmannInstitute of Clinical Anatomy and Cell Analysis, Department of Anatomy, University of Tübingen, Oesterbergstrasse 3, 72074, Tuebingen, Germany.
Anthony GrahamCentre for Developmental Neurobiology, Kings College London, London, SE1 1UL, UK. anthony.graham@kcl.ac.uk.ORCID http://orcid.org/0000-0003-2011-7188
King's College London · GBCharité - Universitätsmedizin Berlin · DEUniversity of Liverpool · GBUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe cells of the mesencephalic trigeminal nucleus (MTN) are the proprioceptive sensory neurons that innervate the jaw closing muscles. These cells differentiate close to the two key signalling centres that influence the dorsal midbrain, the isthmus, which mediates its effects via FGF and WNT signalling and the roof plate, which is a major source of BMP signalling as well as WNT signalling.

methodsIn this study, we have set out to analyse the importance of FGF, WNT and BMP signalling for the development of the MTN. We have employed pharmacological inhibitors of these pathways in explant cultures as well as utilising the electroporation of inhibitory constructs in vivo in the chick embryo.

resultsWe find that interfering with either FGF or WNT signalling has pronounced effects on MTN development whilst abrogation of BMP signalling has no effect. We show that treatment of explants with either FGF or WNT antagonists results in the generation of fewer MTN neurons and affects MTN axon extension and that inhibition of both these pathways has an additive effect. To complement these studies, we have used in vivo electroporation to inhibit BMP, FGF and WNT signalling within dorsal midbrain cells prior to, and during, their differentiation as MTN neurons. Again, we find that inhibition of BMP signalling has no effect on the development of MTN neurons. We additionally find that cells electroporated with inhibitory constructs for either FGF or WNT signalling can differentiate as MTN neurons suggesting that these pathways are not required cell intrinsically for the emergence of these neurons. Indeed, we also show that explants of dorsal mesencephalon lacking both the isthmus and roof plate can generate MTN neurons. However, we did find that inhibiting FGF or WNT signalling had consequences for MTN differentiation.

conclusionsOur results suggest that the emergence of MTN neurons is an intrinsic property of the dorsal mesencephalon of gnathostomes, and that this population undergoes expansion, and maturation, along with the rest of the dorsal midbrain under the influence of FGF and WNT signalling.

Indexed as

AnimalsCell DifferentiationChick EmbryoNeurogenesisNeuronsTegmentum MesencephaliFGFJaw proprioceptionMesencephalic trigeminal nucleusMesVMidbrainMTNWNT BMP

Identifiers

PMID28637511
PMCPMC5480199
OpenAlexW2681024925

What OpenQuestion holds

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LicenceCC BY
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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.