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

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 transcriptom...

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Detalles Bibliográficos
Autores principales: Zhao, Wei, Johnston, Kevin G., Ren, Honglei, Xu, Xiangmin, Nie, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974942/
https://www.ncbi.nlm.nih.gov/pubmed/36854676
http://dx.doi.org/10.1038/s41467-023-36800-w
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author Zhao, Wei
Johnston, Kevin G.
Ren, Honglei
Xu, Xiangmin
Nie, Qing
author_facet Zhao, Wei
Johnston, Kevin G.
Ren, Honglei
Xu, Xiangmin
Nie, Qing
author_sort Zhao, Wei
collection PubMed
description 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.
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spelling pubmed-99749422023-03-02 Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat Zhao, Wei Johnston, Kevin G. Ren, Honglei Xu, Xiangmin Nie, Qing Nat Commun Article 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. Nature Publishing Group UK 2023-02-28 /pmc/articles/PMC9974942/ /pubmed/36854676 http://dx.doi.org/10.1038/s41467-023-36800-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhao, Wei
Johnston, Kevin G.
Ren, Honglei
Xu, Xiangmin
Nie, Qing
Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat
title Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat
title_full Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat
title_fullStr Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat
title_full_unstemmed Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat
title_short Inferring neuron-neuron communications from single-cell transcriptomics through NeuronChat
title_sort inferring neuron-neuron communications from single-cell transcriptomics through neuronchat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974942/
https://www.ncbi.nlm.nih.gov/pubmed/36854676
http://dx.doi.org/10.1038/s41467-023-36800-w
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