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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
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.
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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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