Single nucleus and spatial transcriptomic profiling of healthy human hamstring tendon
The molecular and cellular basis of health in human tendons remains poorly understood. Among human tendons, hamstring tendon has markedly low pathology and can provide a prototypic healthy tendon reference. The aim of this study was to determine the transcriptomes and location of all cell types in h...
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Published in | The FASEB journal Vol. 38; no. 10; pp. e23629 - n/a |
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31.05.2024
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Abstract | The molecular and cellular basis of health in human tendons remains poorly understood. Among human tendons, hamstring tendon has markedly low pathology and can provide a prototypic healthy tendon reference. The aim of this study was to determine the transcriptomes and location of all cell types in healthy hamstring tendon. Using single nucleus RNA sequencing, we profiled the transcriptomes of 10 533 nuclei from four healthy donors and identified 12 distinct cell types. We confirmed the presence of two fibroblast cell types, endothelial cells, mural cells, and immune cells, and identified cell types previously unreported in tendons, including different skeletal muscle cell types, satellite cells, adipocytes, and undefined nervous system cells. The location of these cell types within tendon was defined using spatial transcriptomics and imaging, and potential transcriptional networks and cell–cell interactions were analyzed. We demonstrate that fibroblasts have the highest number of potential cell–cell interactions in our dataset, are present throughout the tendon, and play an important role in the production and organization of extracellular matrix, thus confirming their role as key regulators of hamstring tendon homeostasis. Overall, our findings underscore the complexity of the cellular networks that underpin healthy human tendon function and the central role of fibroblasts as key regulators of hamstring tendon tissue homeostasis.
This study characterized healthy human hamstring tendon using single nucleus RNA‐seq, spatial transcriptomics, and imaging. The resulting reference dataset improves current understanding of the cellular basis of tendon health and will inform future studies of tendon and musculoskeletal disease. Overall, our findings underscore the complexity of the cellular networks that underpin tendon function and the central role of fibroblasts as key regulators of hamstring tendon tissue homeostasis. Graphical was created with BioRender.com. |
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AbstractList | The molecular and cellular basis of health in human tendons remains poorly understood. Among human tendons, hamstring tendon has markedly low pathology and can provide a prototypic healthy tendon reference. The aim of this study was to determine the transcriptomes and location of all cell types in healthy hamstring tendon. Using single nucleus RNA sequencing, we profiled the transcriptomes of 10 533 nuclei from four healthy donors and identified 12 distinct cell types. We confirmed the presence of two fibroblast cell types, endothelial cells, mural cells, and immune cells, and identified cell types previously unreported in tendons, including different skeletal muscle cell types, satellite cells, adipocytes, and undefined nervous system cells. The location of these cell types within tendon was defined using spatial transcriptomics and imaging, and potential transcriptional networks and cell–cell interactions were analyzed. We demonstrate that fibroblasts have the highest number of potential cell–cell interactions in our dataset, are present throughout the tendon, and play an important role in the production and organization of extracellular matrix, thus confirming their role as key regulators of hamstring tendon homeostasis. Overall, our findings underscore the complexity of the cellular networks that underpin healthy human tendon function and the central role of fibroblasts as key regulators of hamstring tendon tissue homeostasis.
This study characterized healthy human hamstring tendon using single nucleus RNA‐seq, spatial transcriptomics, and imaging. The resulting reference dataset improves current understanding of the cellular basis of tendon health and will inform future studies of tendon and musculoskeletal disease. Overall, our findings underscore the complexity of the cellular networks that underpin tendon function and the central role of fibroblasts as key regulators of hamstring tendon tissue homeostasis. Graphical was created with BioRender.com. The molecular and cellular basis of health in human tendons remains poorly understood. Among human tendons, hamstring tendon has markedly low pathology and can provide a prototypic healthy tendon reference. The aim of this study was to determine the transcriptomes and location of all cell types in healthy hamstring tendon. Using single nucleus RNA sequencing, we profiled the transcriptomes of 10 533 nuclei from four healthy donors and identified 12 distinct cell types. We confirmed the presence of two fibroblast cell types, endothelial cells, mural cells, and immune cells, and identified cell types previously unreported in tendons, including different skeletal muscle cell types, satellite cells, adipocytes, and undefined nervous system cells. The location of these cell types within tendon was defined using spatial transcriptomics and imaging, and potential transcriptional networks and cell-cell interactions were analyzed. We demonstrate that fibroblasts have the highest number of potential cell-cell interactions in our dataset, are present throughout the tendon, and play an important role in the production and organization of extracellular matrix, thus confirming their role as key regulators of hamstring tendon homeostasis. Overall, our findings underscore the complexity of the cellular networks that underpin healthy human tendon function and the central role of fibroblasts as key regulators of hamstring tendon tissue homeostasis. |
Author | Paul, Claudia Gwilym, Stephen E. Snelling, Sarah J. B. Ikwuanusi, Chinemerem T. Cribbs, Adam P. Cohen, Carla J. Mimpen, Jolet Y. Kurjan, Alina Hulley, Philippa A. Baldwin, Mathew J. Ramos‐Mucci, Lorenzo |
Author_xml | – sequence: 1 givenname: Jolet Y. orcidid: 0000-0003-4464-242X surname: Mimpen fullname: Mimpen, Jolet Y. email: jolet.mimpen@ndorms.ox.ac.uk organization: University of Oxford – sequence: 2 givenname: Lorenzo orcidid: 0000-0003-4346-8861 surname: Ramos‐Mucci fullname: Ramos‐Mucci, Lorenzo organization: University of Oxford – sequence: 3 givenname: Claudia orcidid: 0000-0001-9729-7135 surname: Paul fullname: Paul, Claudia organization: University of Oxford – sequence: 4 givenname: Alina orcidid: 0000-0002-4503-7865 surname: Kurjan fullname: Kurjan, Alina organization: University of Oxford – sequence: 5 givenname: Philippa A. orcidid: 0000-0002-4994-2264 surname: Hulley fullname: Hulley, Philippa A. organization: University of Oxford – sequence: 6 givenname: Chinemerem T. orcidid: 0009-0006-3517-9575 surname: Ikwuanusi fullname: Ikwuanusi, Chinemerem T. – sequence: 7 givenname: Carla J. orcidid: 0000-0002-8398-0010 surname: Cohen fullname: Cohen, Carla J. organization: Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, University of Oxford – sequence: 8 givenname: Stephen E. orcidid: 0000-0002-1323-8646 surname: Gwilym fullname: Gwilym, Stephen E. organization: University of Oxford – sequence: 9 givenname: Mathew J. orcidid: 0000-0002-8790-9975 surname: Baldwin fullname: Baldwin, Mathew J. organization: University of Oxford – sequence: 10 givenname: Adam P. orcidid: 0000-0001-5288-3077 surname: Cribbs fullname: Cribbs, Adam P. organization: University of Oxford – sequence: 11 givenname: Sarah J. B. orcidid: 0000-0002-7052-3793 surname: Snelling fullname: Snelling, Sarah J. B. organization: University of Oxford |
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Keywords | fibroblasts tendon single nucleus transcriptomics skeletal muscle spatial transcriptomics hamstring |
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Notes | Claudia Paul and Alina Kurjan contributed equally and share the third author position. Jolet Y. Mimpen, Lorenzo Ramos‐Mucci contributed equally and share the first author position. |
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Snippet | The molecular and cellular basis of health in human tendons remains poorly understood. Among human tendons, hamstring tendon has markedly low pathology and can... |
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SubjectTerms | Adult Cell Nucleus - genetics Cell Nucleus - metabolism Extracellular Matrix - metabolism Female fibroblasts Fibroblasts - metabolism Gene Expression Profiling hamstring Hamstring Tendons - metabolism Humans Male single nucleus transcriptomics skeletal muscle spatial transcriptomics tendon Tendons - metabolism Transcriptome |
Title | Single nucleus and spatial transcriptomic profiling of healthy human hamstring tendon |
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