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Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear
In contrast to other mammals, the spiny mouse (Acomys) regenerates skin and ear tissue, which includes hair follicles, glands, and cartilage, in a scar-free manner. Ear punch regeneration is asymmetric with only the proximal wound side participating in regeneration. Here, we show that cues originati...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547259/ https://www.ncbi.nlm.nih.gov/pubmed/37726147 http://dx.doi.org/10.1101/gr.277538.122 |
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author | van Beijnum, Henriëtte Koopmans, Tim Tomasso, Antonio Disela, Vanessa te Lindert, Severin Bakkers, Jeroen Alemany, Anna Berezikov, Eugene Bartscherer, Kerstin |
author_facet | van Beijnum, Henriëtte Koopmans, Tim Tomasso, Antonio Disela, Vanessa te Lindert, Severin Bakkers, Jeroen Alemany, Anna Berezikov, Eugene Bartscherer, Kerstin |
author_sort | van Beijnum, Henriëtte |
collection | PubMed |
description | In contrast to other mammals, the spiny mouse (Acomys) regenerates skin and ear tissue, which includes hair follicles, glands, and cartilage, in a scar-free manner. Ear punch regeneration is asymmetric with only the proximal wound side participating in regeneration. Here, we show that cues originating from the proximal side are required for normal regeneration and use spatially resolved transcriptomics (tomo-seq) to understand the molecular and cellular events underlying this process. Analyzing gene expression across the ear and comparing expression modules between proximal and distal wound sides, we identify asymmetric gene expression patterns and pinpoint regenerative processes in space and time. Moreover, using a comparative approach with nonregenerative rodents (Mus, Meriones), we strengthen a hypothesis in which particularities in the injury-induced immune response may be one of the crucial determinants for why spiny mice regenerate whereas their relatives do not. Our data are available in SpinyMine, an easy-to-use and expandable web-based tool for exploring Acomys regeneration-associated gene expression. |
format | Online Article Text |
id | pubmed-10547259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105472592023-10-04 Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear van Beijnum, Henriëtte Koopmans, Tim Tomasso, Antonio Disela, Vanessa te Lindert, Severin Bakkers, Jeroen Alemany, Anna Berezikov, Eugene Bartscherer, Kerstin Genome Res Resources In contrast to other mammals, the spiny mouse (Acomys) regenerates skin and ear tissue, which includes hair follicles, glands, and cartilage, in a scar-free manner. Ear punch regeneration is asymmetric with only the proximal wound side participating in regeneration. Here, we show that cues originating from the proximal side are required for normal regeneration and use spatially resolved transcriptomics (tomo-seq) to understand the molecular and cellular events underlying this process. Analyzing gene expression across the ear and comparing expression modules between proximal and distal wound sides, we identify asymmetric gene expression patterns and pinpoint regenerative processes in space and time. Moreover, using a comparative approach with nonregenerative rodents (Mus, Meriones), we strengthen a hypothesis in which particularities in the injury-induced immune response may be one of the crucial determinants for why spiny mice regenerate whereas their relatives do not. Our data are available in SpinyMine, an easy-to-use and expandable web-based tool for exploring Acomys regeneration-associated gene expression. Cold Spring Harbor Laboratory Press 2023-08 /pmc/articles/PMC10547259/ /pubmed/37726147 http://dx.doi.org/10.1101/gr.277538.122 Text en © 2023 van Beijnum et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Resources van Beijnum, Henriëtte Koopmans, Tim Tomasso, Antonio Disela, Vanessa te Lindert, Severin Bakkers, Jeroen Alemany, Anna Berezikov, Eugene Bartscherer, Kerstin Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear |
title | Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear |
title_full | Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear |
title_fullStr | Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear |
title_full_unstemmed | Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear |
title_short | Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear |
title_sort | spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (acomys) ear |
topic | Resources |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547259/ https://www.ncbi.nlm.nih.gov/pubmed/37726147 http://dx.doi.org/10.1101/gr.277538.122 |
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