Evidence map›Paper›PMID 36000342›Full record

ArticleMolecular pain2022

Characterisation of deep dorsal horn projection neurons in the spinal cord of the Phox2a::Cre mouse line.

Éva Kókai, Wafa Aa Alsulaiman, Allen C Dickie, Andrew M Bell, Luca Goffin, Masahiko Watanabe, Maria Gutierrez-Mecinas, Andrew J Todd

Open access · goldAbstract read
In one paragraph

Article in Molecular pain, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  9. Deep sequencing of Phox2a nuclei reveals five classes of anterolateral system neurons.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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 2 countries.

Éva KókaiSchool of Psychology and Neuroscience, College of Medical, Veterinary and Life Sciences, 3526University of Glasgow, Glasgow, UK.
Wafa Aa AlsulaimanSchool of Psychology and Neuroscience, College of Medical, Veterinary and Life Sciences, 3526University of Glasgow, Glasgow, UK.
Allen C DickieSchool of Psychology and Neuroscience, College of Medical, Veterinary and Life Sciences, 3526University of Glasgow, Glasgow, UK.ORCID 0000-0002-6339-2801
Andrew M BellSchool of Psychology and Neuroscience, College of Medical, Veterinary and Life Sciences, 3526University of Glasgow, Glasgow, UK.
Luca GoffinSchool of Psychology and Neuroscience, College of Medical, Veterinary and Life Sciences, 3526University of Glasgow, Glasgow, UK.
Masahiko WatanabeDepartment of Anatomy, Hokkaido University School of Medicine, Sapporo, Japan.
Maria Gutierrez-MecinasSchool of Psychology and Neuroscience, College of Medical, Veterinary and Life Sciences, 3526University of Glasgow, Glasgow, UK.
Andrew J ToddSchool of Psychology and Neuroscience, College of Medical, Veterinary and Life Sciences, 3526University of Glasgow, Glasgow, UK.ORCID 0000-0002-3007-6749
University of Glasgow · GBHokkaido University · JP

Funding

Medical Research Council MR/S002987/1Wellcome TrustWellcome Trust 219433/Z/19/Z
6 · The paper itself

Abstract

Projection neurons belonging to the anterolateral system (ALS) underlie the perception of pain, skin temperature and itch. Many ALS cells are located in laminae III-V of the dorsal horn and the adjacent lateral white matter. However, relatively little is known about the excitatory synaptic input to these deep ALS cells, and therefore about their engagement with the neuronal circuitry of the region. We have used a recently developed mouse line, Phox2a::Cre, to investigate a population of deep dorsal horn ALS neurons known as "antenna cells", which are characterised by dense innervation from peptidergic nociceptors, and to compare these with other ALS cells in the deep dorsal horn and lateral white matter. We show that these two classes differ, both in the density of excitatory synapses, and in the source of input at these synapses. Peptidergic nociceptors account for around two-thirds of the excitatory synapses on the antenna cells, but for only a small proportion of the input to the non-antenna cells. Conversely, boutons with high levels of VGLUT2, which are likely to originate mainly from glutamatergic spinal neurons, account for only ∼5% of the excitatory synapses on antenna cells, but for a much larger proportion of the input to the non-antenna cells. VGLUT1 is expressed by myelinated low-threshold mechanoreceptors and corticospinal axons, and these innervate both antenna and non-antenna cells. However, the density of VGLUT1 input to the non-antenna cells is highly variable, consistent with the view that these neurons are functionally heterogeneous.

Indexed as

Posterior Horn CellsSpinal Cord Dorsal HornAnimalsHomeodomain ProteinsIntegrasesMiceCre recombinaseHomeodomain ProteinsIntegrasesPhox2a protein, mouseantenna cellAnterolateral systemlow-threshold mechanoreceptorpeptidergic nociceptorsubstance PTac1

Identifiers

PMID36000342
PMCPMC9445510
OpenAlexW4293169063

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.