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A draft network of ligand–receptor-mediated multicellular signalling in human
Cell-to-cell communication across multiple cell types and tissues strictly governs proper functioning of metazoans and extensively relies on interactions between secreted ligands and cell-surface receptors. Herein, we present the first large-scale map of cell-to-cell communication between 144 human...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525178/ https://www.ncbi.nlm.nih.gov/pubmed/26198319 http://dx.doi.org/10.1038/ncomms8866 |
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author | Ramilowski, Jordan A. Goldberg, Tatyana Harshbarger, Jayson Kloppman, Edda Lizio, Marina Satagopam, Venkata P. Itoh, Masayoshi Kawaji, Hideya Carninci, Piero Rost, Burkhard Forrest, Alistair R. R. |
author_facet | Ramilowski, Jordan A. Goldberg, Tatyana Harshbarger, Jayson Kloppman, Edda Lizio, Marina Satagopam, Venkata P. Itoh, Masayoshi Kawaji, Hideya Carninci, Piero Rost, Burkhard Forrest, Alistair R. R. |
author_sort | Ramilowski, Jordan A. |
collection | PubMed |
description | Cell-to-cell communication across multiple cell types and tissues strictly governs proper functioning of metazoans and extensively relies on interactions between secreted ligands and cell-surface receptors. Herein, we present the first large-scale map of cell-to-cell communication between 144 human primary cell types. We reveal that most cells express tens to hundreds of ligands and receptors to create a highly connected signalling network through multiple ligand–receptor paths. We also observe extensive autocrine signalling with approximately two-thirds of partners possibly interacting on the same cell type. We find that plasma membrane and secreted proteins have the highest cell-type specificity, they are evolutionarily younger than intracellular proteins, and that most receptors had evolved before their ligands. We provide an online tool to interactively query and visualize our networks and demonstrate how this tool can reveal novel cell-to-cell interactions with the prediction that mast cells signal to monoblastic lineages via the CSF1–CSF1R interacting pair. |
format | Online Article Text |
id | pubmed-4525178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45251782015-09-04 A draft network of ligand–receptor-mediated multicellular signalling in human Ramilowski, Jordan A. Goldberg, Tatyana Harshbarger, Jayson Kloppman, Edda Lizio, Marina Satagopam, Venkata P. Itoh, Masayoshi Kawaji, Hideya Carninci, Piero Rost, Burkhard Forrest, Alistair R. R. Nat Commun Article Cell-to-cell communication across multiple cell types and tissues strictly governs proper functioning of metazoans and extensively relies on interactions between secreted ligands and cell-surface receptors. Herein, we present the first large-scale map of cell-to-cell communication between 144 human primary cell types. We reveal that most cells express tens to hundreds of ligands and receptors to create a highly connected signalling network through multiple ligand–receptor paths. We also observe extensive autocrine signalling with approximately two-thirds of partners possibly interacting on the same cell type. We find that plasma membrane and secreted proteins have the highest cell-type specificity, they are evolutionarily younger than intracellular proteins, and that most receptors had evolved before their ligands. We provide an online tool to interactively query and visualize our networks and demonstrate how this tool can reveal novel cell-to-cell interactions with the prediction that mast cells signal to monoblastic lineages via the CSF1–CSF1R interacting pair. Nature Pub. Group 2015-07-22 /pmc/articles/PMC4525178/ /pubmed/26198319 http://dx.doi.org/10.1038/ncomms8866 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ramilowski, Jordan A. Goldberg, Tatyana Harshbarger, Jayson Kloppman, Edda Lizio, Marina Satagopam, Venkata P. Itoh, Masayoshi Kawaji, Hideya Carninci, Piero Rost, Burkhard Forrest, Alistair R. R. A draft network of ligand–receptor-mediated multicellular signalling in human |
title | A draft network of ligand–receptor-mediated multicellular signalling in human |
title_full | A draft network of ligand–receptor-mediated multicellular signalling in human |
title_fullStr | A draft network of ligand–receptor-mediated multicellular signalling in human |
title_full_unstemmed | A draft network of ligand–receptor-mediated multicellular signalling in human |
title_short | A draft network of ligand–receptor-mediated multicellular signalling in human |
title_sort | draft network of ligand–receptor-mediated multicellular signalling in human |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525178/ https://www.ncbi.nlm.nih.gov/pubmed/26198319 http://dx.doi.org/10.1038/ncomms8866 |
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