Literature DB >> 35318675

Development of a cell-free strategy to recover aged skeletal muscle after disuse.

Yu-Fu Wu1,2, Eduardo A De La Toba2,3, Svyatoslav Dvoretskiy1,2, Rebecca Jung2, Noah Kim1,2, Laureen Daniels2,4, Elena V Romanova2,3, Jenny Drnevich5, Jonathan V Sweedler2,3, Marni D Boppart1,2,4.   

Abstract

Extended periods of bed rest and limb immobilization are required for healing post-injury or disease, yet disuse can result in significant muscle atrophy and decreased quality of life in older adults. Physical rehabilitation is commonly prescribed to recover these deficits, yet accumulation of reactive oxygen species and sustained rates of protein degradation persist during the rehabilitation period that can significantly delay or prevent recovery. Pericytes, considered the primary mesenchymal and vascular stromal cell in skeletal muscle, secrete beneficial factors that maintain baseline muscle mass, yet minimal information exists regarding the pericyte response to disuse and recovery. In the current study, single-cell RNA sequencing and functional assays were performed to demonstrate that pericytes in mouse skeletal muscle lose the capacity to synthesize antioxidants during disuse and recovery. This information was used to guide the design of a strategy in which healthy donor pericytes were stimulated with hydrogen peroxide (H2 O2 ) to produce small extracellular vesicles (sEVs) that effectively restored myofibre size in adult and aged muscle after disuse. Proteomic assessment detected 11 differentially regulated proteins in primed sEVs that may account for recovery of muscle, including proteins associated with extracellular matrix composition and anti-inflammatory and antioxidant processes. This study demonstrates that healthy H2 O2 -primed pericyte-derived sEVs effectively improve skeletal muscle recovery after immobilization, presenting a novel acellular approach to rebuild muscle mass in older adults after a period of disuse. KEY POINTS: Previous studies suggest that prolonged oxidative stress is a barrier to skeletal muscle recovery after a period of immobilization. In this study we demonstrate that muscle-resident perivascular stromal cells (pericytes) become dysfunctional and lack the capacity to mount an antioxidant defence after disuse in mice. Hydrogen peroxide treatment of healthy pericytes in vitro simulates the release of small extracellular vesicles (sEVs) that effectively recover skeletal muscle fibre size and extracellular matrix remodelling in young adult and aged mice after disuse. Pericyte-derived sEVs present a novel acellular strategy to recover skeletal muscle after disuse.
© 2022 The Authors. The Journal of Physiology © 2022 The Physiological Society.

Entities:  

Keywords:  antioxidant; disuse atrophy; extracellular vesicles; pericyte; skeletal muscle

Year:  2022        PMID: 35318675      PMCID: PMC9492804          DOI: 10.1113/JP282867

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   6.228


  56 in total

1.  Regrowth after skeletal muscle atrophy is impaired in aged rats, despite similar responses in signaling pathways.

Authors:  Jena R White; Amy L Confides; Stephanie Moore-Reed; Johanna M Hoch; Esther E Dupont-Versteegden
Journal:  Exp Gerontol       Date:  2015-02-12       Impact factor: 4.032

2.  Umbilical cord mesenchymal stem cell-conditioned media prevent muscle atrophy by suppressing muscle atrophy-related proteins and ROS generation.

Authors:  Chan-Mi Park; Mi Jin Kim; Sun-Mi Kim; Jin-Ho Park; Z-Hun Kim; Yong-Soo Choi
Journal:  In Vitro Cell Dev Biol Anim       Date:  2015-09-15       Impact factor: 2.416

3.  Effects of aging on human skeletal muscle after immobilization and retraining.

Authors:  C Suetta; L G Hvid; L Justesen; U Christensen; K Neergaard; L Simonsen; N Ortenblad; S P Magnusson; M Kjaer; P Aagaard
Journal:  J Appl Physiol (1985)       Date:  2009-08-06

4.  Type 2 diabetes impairs the ability of skeletal muscle pericytes to augment postischemic neovascularization in db/db mice.

Authors:  Katherine L Hayes; Louis M Messina; Lawrence M Schwartz; Jinglian Yan; Amy S Burnside; Sarah Witkowski
Journal:  Am J Physiol Cell Physiol       Date:  2018-01-10       Impact factor: 4.249

5.  Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy.

Authors:  Marco Sandri; Claudia Sandri; Alex Gilbert; Carsten Skurk; Elisa Calabria; Anne Picard; Kenneth Walsh; Stefano Schiaffino; Stewart H Lecker; Alfred L Goldberg
Journal:  Cell       Date:  2004-04-30       Impact factor: 41.582

6.  Heme-oxygenase-1-induced protection against hypoxia/reoxygenation is dependent on biliverdin reductase and its interaction with PI3K/Akt pathway.

Authors:  Alok S Pachori; Anthony Smith; Patricia McDonald; Lunan Zhang; Victor J Dzau; Luis G Melo
Journal:  J Mol Cell Cardiol       Date:  2007-08-17       Impact factor: 5.000

7.  Inflammation modulates expression of laminin in the central nervous system following ischemic injury.

Authors:  Kyungmin Ji; Stella E Tsirka
Journal:  J Neuroinflammation       Date:  2012-07-03       Impact factor: 8.322

Review 8.  Can antioxidants protect against disuse muscle atrophy?

Authors:  Scott K Powers
Journal:  Sports Med       Date:  2014-11       Impact factor: 11.136

9.  Normalization and variance stabilization of single-cell RNA-seq data using regularized negative binomial regression.

Authors:  Christoph Hafemeister; Rahul Satija
Journal:  Genome Biol       Date:  2019-12-23       Impact factor: 13.583

10.  Adaptive redox response of mesenchymal stromal cells to stimulation with lipopolysaccharide inflammagen: mechanisms of remodeling of tissue barriers in sepsis.

Authors:  Nikolai V Gorbunov; Bradley R Garrison; Dennis P McDaniel; Min Zhai; Pei-Jyun Liao; Dilber Nurmemet; Juliann G Kiang
Journal:  Oxid Med Cell Longev       Date:  2013-04-18       Impact factor: 6.543

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  1 in total

Review 1.  The Emerging Role of Pericyte-Derived Extracellular Vesicles in Vascular and Neurological Health.

Authors:  Kushal Sharma; Yunpei Zhang; Keshav Raj Paudel; Allan Kachelmeier; Philip M Hansbro; Xiaorui Shi
Journal:  Cells       Date:  2022-10-02       Impact factor: 7.666

  1 in total

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