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Single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments
Ligaments are collagenous connective tissues that connect bones. Injury of knee ligaments, namely anterior cruciate ligament (ACL) and medial collateral ligament (MCL), is common in athletes. Both ligaments have important functions, but distinct regeneration capacities. The capacity for recovery aft...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653455/ https://www.ncbi.nlm.nih.gov/pubmed/36371589 http://dx.doi.org/10.1038/s42003-022-04196-w |
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author | Ishibashi, Kyota Ikegami, Kentaro Shimbo, Takashi Sasaki, Eiji Kitayama, Tomomi Nakamura, Yuzuru Tsushima, Takahiro Ishibashi, Yasuyuki Tamai, Katsuto |
author_facet | Ishibashi, Kyota Ikegami, Kentaro Shimbo, Takashi Sasaki, Eiji Kitayama, Tomomi Nakamura, Yuzuru Tsushima, Takahiro Ishibashi, Yasuyuki Tamai, Katsuto |
author_sort | Ishibashi, Kyota |
collection | PubMed |
description | Ligaments are collagenous connective tissues that connect bones. Injury of knee ligaments, namely anterior cruciate ligament (ACL) and medial collateral ligament (MCL), is common in athletes. Both ligaments have important functions, but distinct regeneration capacities. The capacity for recovery after injury also diminishes with age. However, cellular heterogeneity in the ligaments remains unclear. Here, we profiled the transcriptional signatures of ACL and MCL cells in mice using single-cell RNA sequencing. These ligaments comprise three fibroblast types expressing Col22a1, Col12a1, or Col14a1, but have distinct localizations in the tissue. We found substantial heterogeneity in Col12a1- and Col14a1-positive cells between ACL and MCL. Gene Ontology analysis revealed that angiogenesis- and collagen regulation-related genes were specifically enriched in MCL cells. Furthermore, we identified age-related changes in cell composition and gene expression in the ligaments. This study delineates cellular heterogeneity in ligaments, serving as a foundation for identifying potential therapeutic targets for ligament injuries. |
format | Online Article Text |
id | pubmed-9653455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96534552022-11-15 Single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments Ishibashi, Kyota Ikegami, Kentaro Shimbo, Takashi Sasaki, Eiji Kitayama, Tomomi Nakamura, Yuzuru Tsushima, Takahiro Ishibashi, Yasuyuki Tamai, Katsuto Commun Biol Article Ligaments are collagenous connective tissues that connect bones. Injury of knee ligaments, namely anterior cruciate ligament (ACL) and medial collateral ligament (MCL), is common in athletes. Both ligaments have important functions, but distinct regeneration capacities. The capacity for recovery after injury also diminishes with age. However, cellular heterogeneity in the ligaments remains unclear. Here, we profiled the transcriptional signatures of ACL and MCL cells in mice using single-cell RNA sequencing. These ligaments comprise three fibroblast types expressing Col22a1, Col12a1, or Col14a1, but have distinct localizations in the tissue. We found substantial heterogeneity in Col12a1- and Col14a1-positive cells between ACL and MCL. Gene Ontology analysis revealed that angiogenesis- and collagen regulation-related genes were specifically enriched in MCL cells. Furthermore, we identified age-related changes in cell composition and gene expression in the ligaments. This study delineates cellular heterogeneity in ligaments, serving as a foundation for identifying potential therapeutic targets for ligament injuries. Nature Publishing Group UK 2022-11-12 /pmc/articles/PMC9653455/ /pubmed/36371589 http://dx.doi.org/10.1038/s42003-022-04196-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ishibashi, Kyota Ikegami, Kentaro Shimbo, Takashi Sasaki, Eiji Kitayama, Tomomi Nakamura, Yuzuru Tsushima, Takahiro Ishibashi, Yasuyuki Tamai, Katsuto Single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments |
title | Single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments |
title_full | Single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments |
title_fullStr | Single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments |
title_full_unstemmed | Single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments |
title_short | Single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments |
title_sort | single-cell transcriptome analysis reveals cellular heterogeneity in mouse intra- and extra articular ligaments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653455/ https://www.ncbi.nlm.nih.gov/pubmed/36371589 http://dx.doi.org/10.1038/s42003-022-04196-w |
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