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Research perspectives—Pipelines to human tendon transcriptomics

Tendon transcriptomics is a rapidly growing field in musculoskeletal biology. The ultimate aim of many current tendon transcriptomic studies is characterization of in vitro, ex vivo, or in vivo, healthy, and diseased tendon microenvironments to identify the underlying pathways driving human tendon p...

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Autores principales: Ramos‐Mucci, Lorenzo, Sarmiento, Paula, Little, Dianne, Snelling, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007907/
https://www.ncbi.nlm.nih.gov/pubmed/35239195
http://dx.doi.org/10.1002/jor.25315
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author Ramos‐Mucci, Lorenzo
Sarmiento, Paula
Little, Dianne
Snelling, Sarah
author_facet Ramos‐Mucci, Lorenzo
Sarmiento, Paula
Little, Dianne
Snelling, Sarah
author_sort Ramos‐Mucci, Lorenzo
collection PubMed
description Tendon transcriptomics is a rapidly growing field in musculoskeletal biology. The ultimate aim of many current tendon transcriptomic studies is characterization of in vitro, ex vivo, or in vivo, healthy, and diseased tendon microenvironments to identify the underlying pathways driving human tendon pathology. The transcriptome interfaces between genomic, proteomic, and metabolomic signatures of the tendon cellular niche and the response of this niche to stimuli. Some of the greatest bottlenecks in tendon transcriptomics relate to the availability and quality of human tendon tissue, hence animal tissues are frequently used even though human tissue is most translationally relevant. Here, we review the variability associated with human donor and procurement factors, such as whether the tendon is cadaveric or a clinical remnant, and how these variables affect the quality and relevance of the transcriptomes obtained. Moreover, age, sex, and health demographic variables impact the human tendon transcriptome. Tendons present tissue‐specific challenges for cell, nuclei, and RNA extraction that include a dense extracellular matrix, low cellularity, and therefore low RNA yield of variable quality. Consideration of these factors is particularly important for single‐cell and single‐nuclei resolution transcriptomics due to the necessity for unbiased and representative cell or nuclei populations. Different cell, nuclei, and RNA extraction methods, library preparation, and quality control methods are used by the tendon research community and attention should be paid to these when designing and reporting studies. We discuss the different components and challenges of human tendon transcriptomics, and propose pipelines, quality control, and reporting guidelines for future work in the field.
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spelling pubmed-90079072022-10-14 Research perspectives—Pipelines to human tendon transcriptomics Ramos‐Mucci, Lorenzo Sarmiento, Paula Little, Dianne Snelling, Sarah J Orthop Res REVIEW Tendon transcriptomics is a rapidly growing field in musculoskeletal biology. The ultimate aim of many current tendon transcriptomic studies is characterization of in vitro, ex vivo, or in vivo, healthy, and diseased tendon microenvironments to identify the underlying pathways driving human tendon pathology. The transcriptome interfaces between genomic, proteomic, and metabolomic signatures of the tendon cellular niche and the response of this niche to stimuli. Some of the greatest bottlenecks in tendon transcriptomics relate to the availability and quality of human tendon tissue, hence animal tissues are frequently used even though human tissue is most translationally relevant. Here, we review the variability associated with human donor and procurement factors, such as whether the tendon is cadaveric or a clinical remnant, and how these variables affect the quality and relevance of the transcriptomes obtained. Moreover, age, sex, and health demographic variables impact the human tendon transcriptome. Tendons present tissue‐specific challenges for cell, nuclei, and RNA extraction that include a dense extracellular matrix, low cellularity, and therefore low RNA yield of variable quality. Consideration of these factors is particularly important for single‐cell and single‐nuclei resolution transcriptomics due to the necessity for unbiased and representative cell or nuclei populations. Different cell, nuclei, and RNA extraction methods, library preparation, and quality control methods are used by the tendon research community and attention should be paid to these when designing and reporting studies. We discuss the different components and challenges of human tendon transcriptomics, and propose pipelines, quality control, and reporting guidelines for future work in the field. John Wiley and Sons Inc. 2022-03-16 2022-05 /pmc/articles/PMC9007907/ /pubmed/35239195 http://dx.doi.org/10.1002/jor.25315 Text en © 2022 The Authors. Journal of Orthopaedic Research® published by Wiley Periodicals LLC on behalf of Orthopaedic Research Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle REVIEW
Ramos‐Mucci, Lorenzo
Sarmiento, Paula
Little, Dianne
Snelling, Sarah
Research perspectives—Pipelines to human tendon transcriptomics
title Research perspectives—Pipelines to human tendon transcriptomics
title_full Research perspectives—Pipelines to human tendon transcriptomics
title_fullStr Research perspectives—Pipelines to human tendon transcriptomics
title_full_unstemmed Research perspectives—Pipelines to human tendon transcriptomics
title_short Research perspectives—Pipelines to human tendon transcriptomics
title_sort research perspectives—pipelines to human tendon transcriptomics
topic REVIEW
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007907/
https://www.ncbi.nlm.nih.gov/pubmed/35239195
http://dx.doi.org/10.1002/jor.25315
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