Evidence map›Paper›PMID 29686262›Full record

ArticleNature neuroscience2018

Neuronal atlas of the dorsal horn defines its architecture and links sensory input to transcriptional cell types.

Martin Häring, Amit Zeisel, Hannah Hochgerner, Puneet Rinwa, Jon E T Jakobsson, Peter Lönnerberg, Gioele La Manno, Nilesh Sharma, Lotta Borgius, Ole Kiehn and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 257 papers.

0numbers the graph read from it
0cells of the map it votes in
257citing papers in PubMed
24.0field-weighted citation impact, top 1% 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

257 citing papers in PubMed, 486 citations in OpenAlex.

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  12. A Tac1-Expressing Brainstem Pathway Underlies the Pathogenesis of Trigeminal Neuralgia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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197 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 2 countries.

Martin HäringDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
Amit ZeiselDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
Hannah HochgernerDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-7739-666X
Puneet RinwaDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
Jon E T JakobssonDepartment of Neuroscience, Uppsala University, Uppsala, Sweden.
Peter LönnerbergDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
Gioele La MannoDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
Nilesh SharmaDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
Lotta BorgiusMammalian Locomotor Laboratory, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Ole KiehnMammalian Locomotor Laboratory, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Malin C LagerströmDepartment of Neuroscience, Uppsala University, Uppsala, Sweden.
Sten LinnarssonDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden. sten.linnarsson@ki.se.ORCID http://orcid.org/0000-0002-3491-3444
Patrik ErnforsDivision of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden. patrik.ernfors@ki.se.ORCID http://orcid.org/0000-0002-1140-3986
Karolinska Institutet · SEUppsala University · SEUniversity of Copenhagen · DK

Funding

Wellcome Trust 200183/Z/15/Z
6 · The paper itself

Abstract

The dorsal horn of the spinal cord is critical to processing distinct modalities of noxious and innocuous sensation, but little is known of the neuronal subtypes involved, hampering efforts to deduce principles governing somatic sensation. Here we used single-cell RNA sequencing to classify sensory neurons in the mouse dorsal horn. We identified 15 inhibitory and 15 excitatory molecular subtypes of neurons, equaling the complexity in cerebral cortex. Validating our classification scheme in vivo and matching cell types to anatomy of the dorsal horn by spatial transcriptomics reveals laminar enrichment for each of the cell types. Neuron types, when combined, define a multilayered organization with like neurons layered together. Employing our scheme, we find that heat and cold stimuli activate discrete sets of both excitatory and inhibitory neuron types. This work provides a systematic and comprehensive molecular classification of spinal cord sensory neurons, enabling functional interrogation of sensory processing.

Indexed as

Atlases as TopicAnimalsCold TemperatureFemaleGlutamatesHot TemperatureMaleMiceMice, Inbred C57BLNeural PathwaysNeuronsPosterior Horn CellsRNASensationSensory Receptor CellsSpinal CordGlutamatesRNA

Identifiers

PMID29686262
OpenAlexW2800339537

What OpenQuestion holds

Textmetadata
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.