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Inferring a spatial code of cell-cell interactions across a whole animal body

Cell-cell interactions shape cellular function and ultimately organismal phenotype. Interacting cells can sense their mutual distance using combinations of ligand-receptor pairs, suggesting the existence of a spatial code, i.e., signals encoding spatial properties of cellular organization. However,...

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Autores principales: Armingol, Erick, Ghaddar, Abbas, Joshi, Chintan J., Baghdassarian, Hratch, Shamie, Isaac, Chan, Jason, Her, Hsuan-Lin, Berhanu, Samuel, Dar, Anushka, Rodriguez-Armstrong, Fabiola, Yang, Olivia, O’Rourke, Eyleen J., Lewis, Nathan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714814/
https://www.ncbi.nlm.nih.gov/pubmed/36395331
http://dx.doi.org/10.1371/journal.pcbi.1010715
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author Armingol, Erick
Ghaddar, Abbas
Joshi, Chintan J.
Baghdassarian, Hratch
Shamie, Isaac
Chan, Jason
Her, Hsuan-Lin
Berhanu, Samuel
Dar, Anushka
Rodriguez-Armstrong, Fabiola
Yang, Olivia
O’Rourke, Eyleen J.
Lewis, Nathan E.
author_facet Armingol, Erick
Ghaddar, Abbas
Joshi, Chintan J.
Baghdassarian, Hratch
Shamie, Isaac
Chan, Jason
Her, Hsuan-Lin
Berhanu, Samuel
Dar, Anushka
Rodriguez-Armstrong, Fabiola
Yang, Olivia
O’Rourke, Eyleen J.
Lewis, Nathan E.
author_sort Armingol, Erick
collection PubMed
description Cell-cell interactions shape cellular function and ultimately organismal phenotype. Interacting cells can sense their mutual distance using combinations of ligand-receptor pairs, suggesting the existence of a spatial code, i.e., signals encoding spatial properties of cellular organization. However, this code driving and sustaining the spatial organization of cells remains to be elucidated. Here we present a computational framework to infer the spatial code underlying cell-cell interactions from the transcriptomes of the cell types across the whole body of a multicellular organism. As core of this framework, we introduce our tool cell2cell, which uses the coexpression of ligand-receptor pairs to compute the potential for intercellular interactions, and we test it across the Caenorhabditis elegans’ body. Leveraging a 3D atlas of C. elegans’ cells, we also implement a genetic algorithm to identify the ligand-receptor pairs most informative of the spatial organization of cells across the whole body. Validating the spatial code extracted with this strategy, the resulting intercellular distances are negatively correlated with the inferred cell-cell interactions. Furthermore, for selected cell-cell and ligand-receptor pairs, we experimentally confirm the communicatory behavior inferred with cell2cell and the genetic algorithm. Thus, our framework helps identify a code that predicts the spatial organization of cells across a whole-animal body.
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spelling pubmed-97148142022-12-02 Inferring a spatial code of cell-cell interactions across a whole animal body Armingol, Erick Ghaddar, Abbas Joshi, Chintan J. Baghdassarian, Hratch Shamie, Isaac Chan, Jason Her, Hsuan-Lin Berhanu, Samuel Dar, Anushka Rodriguez-Armstrong, Fabiola Yang, Olivia O’Rourke, Eyleen J. Lewis, Nathan E. PLoS Comput Biol Research Article Cell-cell interactions shape cellular function and ultimately organismal phenotype. Interacting cells can sense their mutual distance using combinations of ligand-receptor pairs, suggesting the existence of a spatial code, i.e., signals encoding spatial properties of cellular organization. However, this code driving and sustaining the spatial organization of cells remains to be elucidated. Here we present a computational framework to infer the spatial code underlying cell-cell interactions from the transcriptomes of the cell types across the whole body of a multicellular organism. As core of this framework, we introduce our tool cell2cell, which uses the coexpression of ligand-receptor pairs to compute the potential for intercellular interactions, and we test it across the Caenorhabditis elegans’ body. Leveraging a 3D atlas of C. elegans’ cells, we also implement a genetic algorithm to identify the ligand-receptor pairs most informative of the spatial organization of cells across the whole body. Validating the spatial code extracted with this strategy, the resulting intercellular distances are negatively correlated with the inferred cell-cell interactions. Furthermore, for selected cell-cell and ligand-receptor pairs, we experimentally confirm the communicatory behavior inferred with cell2cell and the genetic algorithm. Thus, our framework helps identify a code that predicts the spatial organization of cells across a whole-animal body. Public Library of Science 2022-11-17 /pmc/articles/PMC9714814/ /pubmed/36395331 http://dx.doi.org/10.1371/journal.pcbi.1010715 Text en © 2022 Armingol et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Armingol, Erick
Ghaddar, Abbas
Joshi, Chintan J.
Baghdassarian, Hratch
Shamie, Isaac
Chan, Jason
Her, Hsuan-Lin
Berhanu, Samuel
Dar, Anushka
Rodriguez-Armstrong, Fabiola
Yang, Olivia
O’Rourke, Eyleen J.
Lewis, Nathan E.
Inferring a spatial code of cell-cell interactions across a whole animal body
title Inferring a spatial code of cell-cell interactions across a whole animal body
title_full Inferring a spatial code of cell-cell interactions across a whole animal body
title_fullStr Inferring a spatial code of cell-cell interactions across a whole animal body
title_full_unstemmed Inferring a spatial code of cell-cell interactions across a whole animal body
title_short Inferring a spatial code of cell-cell interactions across a whole animal body
title_sort inferring a spatial code of cell-cell interactions across a whole animal body
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714814/
https://www.ncbi.nlm.nih.gov/pubmed/36395331
http://dx.doi.org/10.1371/journal.pcbi.1010715
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