Literature DB >> 36267539

Discovery of Muscle-Tendon Progenitor Subpopulation in Human Myotendinous Junction at Single-Cell Resolution.

Ruojin Yan1,2,3, Hong Zhang1,2,3,4, Yuanzhu Ma1,2,3,5, Ruifu Lin1,2,3, Bo Zhou1,2,3, Tao Zhang1,2,3, Chunmei Fan1,2,3, Yuxiang Zhang1,2,3, Zetao Wang1,2,3, Tianshun Fang1,2,3, Zi Yin2,3,4, Youzhi Cai6, Hongwei Ouyang1,2,3,5, Xiao Chen1,2,3,5.   

Abstract

The myotendinous junction (MTJ) is a complex and special anatomical area that connects muscles and tendons, and it is also the key to repairing tendons. Nevertheless, the anatomical structure and connection structure of MTJ, the cluster and distribution of cells, and which cells are involved in repairing the tissue are still unclear. Here, we analyzed the cell subtype distribution and function of human MTJ at single-cell level. We identified four main subtypes, including stem cell, muscle, tendon, and muscle-tendon progenitor cells (MTP). The MTP subpopulation, which remains the characteristics of stem cells and also expresses muscle and tendon marker genes simultaneously, may have the potential for bidirectional differentiation. We also found the muscle-tendon progenitor cells were distributed in the shape of a transparent goblet; muscle cells first connect to the MTP and then to the tendon. And after being transplanted in the MTJ injury model, MTP exhibited strong regenerative capability. Finally, we also demonstrated the importance of mTOR signaling for MTP maintenance by in vitro addition of rapamycin and in vivo validation using mTOR-ko mice. Our research conducted a comprehensive analysis of the heterogeneity of myotendinous junction, discovered a special cluster called MTP, provided new insights into the biological significance of myotendinous junction, and laid the foundation for future research on myotendinous junction regeneration and restoration.
Copyright © 2022 Ruojin Yan et al.

Entities:  

Year:  2022        PMID: 36267539      PMCID: PMC9555880          DOI: 10.34133/2022/9760390

Source DB:  PubMed          Journal:  Research (Wash D C)        ISSN: 2639-5274


  33 in total

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Journal:  Clin Podiatr Med Surg       Date:  2005-10       Impact factor: 1.231

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Journal:  Nature       Date:  2017-06-14       Impact factor: 49.962

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Authors:  Biljana Ilkovski; Sophie Clement; Caroline Sewry; Kathryn N North; Sandra T Cooper
Journal:  Neuromuscul Disord       Date:  2005-11-08       Impact factor: 4.296

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7.  Simultaneous expression of skeletal muscle and heart actin proteins in various striated muscle tissues and cells. A quantitative determination of the two actin isoforms.

Authors:  J Vandekerckhove; G Bugaisky; M Buckingham
Journal:  J Biol Chem       Date:  1986-02-05       Impact factor: 5.157

8.  Altered Skeletal Muscle Mitochondrial Proteome As the Basis of Disruption of Mitochondrial Function in Diabetic Mice.

Authors:  Piotr Zabielski; Ian R Lanza; Srinivas Gopala; Carrie J Holtz Heppelmann; H Robert Bergen; Surendra Dasari; K Sreekumaran Nair
Journal:  Diabetes       Date:  2015-12-30       Impact factor: 9.461

9.  Single-nucleus RNA-seq identifies transcriptional heterogeneity in multinucleated skeletal myofibers.

Authors:  Michael J Petrany; Casey O Swoboda; Chengyi Sun; Kashish Chetal; Xiaoting Chen; Matthew T Weirauch; Nathan Salomonis; Douglas P Millay
Journal:  Nat Commun       Date:  2020-12-11       Impact factor: 14.919

10.  Single-Cell Transcriptomic Analysis of Primary and Metastatic Tumor Ecosystems in Head and Neck Cancer.

Authors:  Sidharth V Puram; Itay Tirosh; Anuraag S Parikh; Anoop P Patel; Keren Yizhak; Shawn Gillespie; Christopher Rodman; Christina L Luo; Edmund A Mroz; Kevin S Emerick; Daniel G Deschler; Mark A Varvares; Ravi Mylvaganam; Orit Rozenblatt-Rosen; James W Rocco; William C Faquin; Derrick T Lin; Aviv Regev; Bradley E Bernstein
Journal:  Cell       Date:  2017-11-30       Impact factor: 41.582

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