Evidence map›Paper›PMID 40161840›Full record

ArticlebioRxiv : the preprint server for biology2025

Ontogeny of the spinal cord dorsal horn.

Robert Brian Roome, Archana Yadav, Lydia Flores, Amrit Puarr, Diana Nardini, Alexander Richardson, Ronald R Waclaw, Ruth M Arkell, Vilas Menon, Jane E Johnson and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Robert Brian RoomeSpinal Circuits and Plasticity Unit, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID 0009-0009-6050-7368
Archana YadavCenter for Translational and Computational Neuroimmunology, Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.
Lydia FloresDepartment of Neuroscience, UT Southwestern Medical Center, Dallas, TX, USA.
Amrit PuarrMaternal-foetal Precision Health Laboratory, John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.ORCID 0009-0001-0359-8832
Diana NardiniExperimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.ORCID 0000-0002-7121-4343
Alexander RichardsonSpinal Circuits and Plasticity Unit, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Ronald R WaclawExperimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.ORCID 0000-0003-4204-4370
Ruth M ArkellMaternal-foetal Precision Health Laboratory, John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.ORCID 0000-0002-6213-7323
Vilas MenonCenter for Translational and Computational Neuroimmunology, Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0002-4096-8601
Jane E JohnsonDepartment of Neuroscience, UT Southwestern Medical Center, Dallas, TX, USA.
Ariel J LevineSpinal Circuits and Plasticity Unit, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID 0000-0002-0335-0730

Funding

Mechanisms of Plasticity in the Spinal CordZIANS003153 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI LEVINE, ARIEL · 2016 to 2025
$20.9M
Data Analysis CoreU54AG076040 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PHATNANI, HEMALI · 2021 to 2025
$13.1M
Transcription Factor Control of Neuronal DiversityR37HD091856 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI Jane E Johnson · 2017 to 2026
$4.7M
Intramural NIH HHS ZIA NS003153NIA NIH HHS U54 AG076040NICHD NIH HHS R37 HD091856
6 · The paper itself

Abstract

The dorsal horn of the mammalian spinal cord is an exquisite example of form serving function. It is comprised of diverse neuronal populations stacked into laminae, each of which receives different circuit connections and plays specialized roles in behavior. An outstanding question is how this organization emerges during development from an apparently homogeneous pool of neural progenitors. Here, we found that dorsal neurons are diversified by time, with families of related cell types born as temporal cohorts, and by a spatial-molecular gradient that specifies the full array of individual cell types. Excitatory dorsal neurons then settle in a chronotopic arrangement that transforms their progressive birthdates into anatomical order. This establishes the dorsal horn laminae, as these neurons are also required for spatial organization of inhibitory neurons and sensory axons. This work reveals essential ontogenetic principles that shape dorsal progenitors into the diverse cell types and architecture that subserve sensorimotor behavior.

Indexed as

cell typesdevelopmentdorsal horninterneuronslaminaontogenySpinal cordstructuretemporal specificationZic

Identifiers

PMID40161840
PMCPMC11952496

What OpenQuestion holds

Textmetadata
LicenceCC0
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.