Cargando…
Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells
Syncytial skeletal muscle cells contain hundreds of nuclei in a shared cytoplasm. We investigated nuclear heterogeneity and transcriptional dynamics in the uninjured and regenerating muscle using single-nucleus RNA-sequencing (snRNAseq) of isolated nuclei from muscle fibers. This revealed distinct n...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732842/ https://www.ncbi.nlm.nih.gov/pubmed/33311457 http://dx.doi.org/10.1038/s41467-020-20064-9 |
_version_ | 1783622175975014400 |
---|---|
author | Kim, Minchul Franke, Vedran Brandt, Bettina Lowenstein, Elijah D. Schöwel, Verena Spuler, Simone Akalin, Altuna Birchmeier, Carmen |
author_facet | Kim, Minchul Franke, Vedran Brandt, Bettina Lowenstein, Elijah D. Schöwel, Verena Spuler, Simone Akalin, Altuna Birchmeier, Carmen |
author_sort | Kim, Minchul |
collection | PubMed |
description | Syncytial skeletal muscle cells contain hundreds of nuclei in a shared cytoplasm. We investigated nuclear heterogeneity and transcriptional dynamics in the uninjured and regenerating muscle using single-nucleus RNA-sequencing (snRNAseq) of isolated nuclei from muscle fibers. This revealed distinct nuclear subtypes unrelated to fiber type diversity, previously unknown subtypes as well as the expected ones at the neuromuscular and myotendinous junctions. In fibers of the Mdx dystrophy mouse model, distinct subtypes emerged, among them nuclei expressing a repair signature that were also abundant in the muscle of dystrophy patients, and a nuclear population associated with necrotic fibers. Finally, modifications of our approach revealed the compartmentalization in the rare and specialized muscle spindle. Our data identifies nuclear compartments of the myofiber and defines a molecular roadmap for their functional analyses; the data can be freely explored on the MyoExplorer server (https://shiny.mdc-berlin.de/MyoExplorer/). |
format | Online Article Text |
id | pubmed-7732842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77328422020-12-17 Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells Kim, Minchul Franke, Vedran Brandt, Bettina Lowenstein, Elijah D. Schöwel, Verena Spuler, Simone Akalin, Altuna Birchmeier, Carmen Nat Commun Article Syncytial skeletal muscle cells contain hundreds of nuclei in a shared cytoplasm. We investigated nuclear heterogeneity and transcriptional dynamics in the uninjured and regenerating muscle using single-nucleus RNA-sequencing (snRNAseq) of isolated nuclei from muscle fibers. This revealed distinct nuclear subtypes unrelated to fiber type diversity, previously unknown subtypes as well as the expected ones at the neuromuscular and myotendinous junctions. In fibers of the Mdx dystrophy mouse model, distinct subtypes emerged, among them nuclei expressing a repair signature that were also abundant in the muscle of dystrophy patients, and a nuclear population associated with necrotic fibers. Finally, modifications of our approach revealed the compartmentalization in the rare and specialized muscle spindle. Our data identifies nuclear compartments of the myofiber and defines a molecular roadmap for their functional analyses; the data can be freely explored on the MyoExplorer server (https://shiny.mdc-berlin.de/MyoExplorer/). Nature Publishing Group UK 2020-12-11 /pmc/articles/PMC7732842/ /pubmed/33311457 http://dx.doi.org/10.1038/s41467-020-20064-9 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Kim, Minchul Franke, Vedran Brandt, Bettina Lowenstein, Elijah D. Schöwel, Verena Spuler, Simone Akalin, Altuna Birchmeier, Carmen Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells |
title | Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells |
title_full | Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells |
title_fullStr | Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells |
title_full_unstemmed | Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells |
title_short | Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells |
title_sort | single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732842/ https://www.ncbi.nlm.nih.gov/pubmed/33311457 http://dx.doi.org/10.1038/s41467-020-20064-9 |
work_keys_str_mv | AT kimminchul singlenucleustranscriptomicsrevealsfunctionalcompartmentalizationinsyncytialskeletalmusclecells AT frankevedran singlenucleustranscriptomicsrevealsfunctionalcompartmentalizationinsyncytialskeletalmusclecells AT brandtbettina singlenucleustranscriptomicsrevealsfunctionalcompartmentalizationinsyncytialskeletalmusclecells AT lowensteinelijahd singlenucleustranscriptomicsrevealsfunctionalcompartmentalizationinsyncytialskeletalmusclecells AT schowelverena singlenucleustranscriptomicsrevealsfunctionalcompartmentalizationinsyncytialskeletalmusclecells AT spulersimone singlenucleustranscriptomicsrevealsfunctionalcompartmentalizationinsyncytialskeletalmusclecells AT akalinaltuna singlenucleustranscriptomicsrevealsfunctionalcompartmentalizationinsyncytialskeletalmusclecells AT birchmeiercarmen singlenucleustranscriptomicsrevealsfunctionalcompartmentalizationinsyncytialskeletalmusclecells |