Evidence map›Paper›PMID 36854676›Full record

ArticleNature communications2023

Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat.

Wei Zhao, Kevin G Johnston, Honglei Ren, Xiangmin Xu, Qing Nie

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
10.9field-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

58 citing papers in PubMed, 71 citations in OpenAlex.

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  14. Aberrant Splicing Signatures Underpin Oligodendrocyte Damage in ALS and Neuron Loss in FTD.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

5 authors at 1 institution in 1 country.

Wei ZhaoDepartment of Mathematics and the NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, CA, 92697, USA.ORCID 0000-0003-1241-5652
Kevin G JohnstonDepartment of Mathematics and the NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, CA, 92697, USA.
Honglei RenDepartment of Mathematics and the NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, CA, 92697, USA.
Xiangmin XuDepartment of Anatomy and Neurobiology, School of Medicine, University of California, Irvine, CA, 92697, USA.ORCID 0000-0002-5828-1533
Qing NieDepartment of Mathematics and the NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, CA, 92697, USA. qnie@uci.edu.ORCID 0000-0002-8804-3368
University of California, Irvine · US

Funding

Cell-type-specific neural circuit connectomes in the mouse models of aging and Alzheimer's diseaseU01AG076791 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI Kim Green, ERAN A MUKAMEL · 2022 to 2026
$13.6M
Subiculm circuits for cortical feedback regulation of spatial mapping and learningR01NS104897 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI NITZ, DOUGLAS ARTHUR, XU, XIANGMIN · 2018 to 2022
$2.6M
NIA NIH HHS U01 AG076791NINDS NIH HHS R01 NS104897Wellcome Trust
6 · The paper itself

Abstract

Neural communication networks form the fundamental basis for brain function. These communication networks are enabled by emitted ligands such as neurotransmitters, which activate receptor complexes to facilitate communication. Thus, neural communication is fundamentally dependent on the transcriptome. Here we develop NeuronChat, a method and package for the inference, visualization and analysis of neural-specific communication networks among pre-defined cell groups using single-cell expression data. We incorporate a manually curated molecular interaction database of neural signaling for both human and mouse, and benchmark NeuronChat on several published datasets to validate its ability in predicting neural connectivity. Then, we apply NeuronChat to three different neural tissue datasets to illustrate its functionalities in identifying interneural communication networks, revealing conserved or context-specific interactions across different biological contexts, and predicting communication pattern changes in diseased brains with autism spectrum disorder. Finally, we demonstrate NeuronChat can utilize spatial transcriptomics data to infer and visualize neural-specific cell-cell communication.

Indexed as

Autism Spectrum DisorderNerve TissueAnimalsGene Expression ProfilingHumansMiceNeuronsTranscriptome

Identifiers

PMID36854676
PMCPMC9974942
OpenAlexW4322720350

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.