Evidence map›Paper›PMID 37845544›Full record

ArticleNature neuroscience2023

Spatial transcriptomics reveals the distinct organization of mouse prefrontal cortex and neuronal subtypes regulating chronic pain.

Aritra Bhattacherjee, Chao Zhang, Brianna R Watson, Mohamed Nadhir Djekidel, Jeffrey R Moffitt, Yi Zhang

Erratum issuedAbstract read
In one paragraph

Article in Nature neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
–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

52 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. A pathway from the anterior cingulate cortex to the lateral habenula controls chronic pain-induced depression in male mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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  20. Artificial Intelligence Revolution in Transcriptomics: From Single Cells to Spatial Atlases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Aritra Bhattacherjee *Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.
Chao Zhang *Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0003-4167-4872
Brianna R WatsonProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0001-6540-5330
Mohamed Nadhir DjekidelHoward Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0001-5361-1858
Jeffrey R MoffittProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA. jeffrey.moffitt@childrens.harvard.edu.ORCID 0000-0002-3836-3101
Yi ZhangHoward Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA. yzhang@genetics.med.harvard.edu.ORCID 0000-0002-2789-0811

Funding

Understanding neuronal subtype-specific function of NAc in cocaine addictionR01DA050589 · NIDA · BOSTON CHILDREN'S HOSPITAL · PI ZHANG, YI · 2021 to 2025
$3.7M
Role of DNA Methylation in Cocaine AddictionR01DA042283 · NIDA · BOSTON CHILDREN'S HOSPITAL · PI ZHANG, YI · 2017 to 2021
$2.8M
NIDA NIH HHS R01 DA042283NIDA NIH HHS R01 DA050589
6 · The paper itself

Abstract

The prefrontal cortex (PFC) is a complex brain region that regulates diverse functions ranging from cognition, emotion and executive action to even pain processing. To decode the cellular and circuit organization of such diverse functions, we employed spatially resolved single-cell transcriptome profiling of the adult mouse PFC. Results revealed that PFC has distinct cell-type composition and gene-expression patterns relative to neighboring cortical areas-with neuronal excitability-regulating genes differently expressed. These cellular and molecular features are further segregated within PFC subregions, alluding to the subregion-specificity of several PFC functions. PFC projects to major subcortical targets through combinations of neuronal subtypes, which emerge in a target-intrinsic fashion. Finally, based on these features, we identified distinct cell types and circuits in PFC underlying chronic pain, an escalating healthcare challenge with limited molecular understanding. Collectively, this comprehensive map will facilitate decoding of discrete molecular, cellular and circuit mechanisms underlying specific PFC functions in health and disease.

Indexed as

Chronic PainTranscriptomeAnimalsCognitionGene Expression ProfilingMicePrefrontal Cortex

Identifiers

PMID37845544
PMCPMC10620082

What OpenQuestion holds

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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.