Evidence map›Paper›PMID 33256005›Full record

ArticleCells2020

Muscle Stem Cell-Derived Extracellular Vesicles Reverse Hydrogen Peroxide-Induced Mitochondrial Dysfunction in Mouse Myotubes.

Kyle T Shuler, Brittany E Wilson, Eric R Muñoz, Andrew D Mitchell, Joshua T Selsby, Matthew B Hudson

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 21 citations in OpenAlex.

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  12. Fusion and beyond: Satellite cell contributions to loading-induced skeletal muscle adaptation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Kyle T ShulerDepartment of Kinesiology and Applied Physiology, University of Delaware, 540 S College Ave, Newark, DE 19713, USA.ORCID 0000-0001-5948-4714
Brittany E WilsonDepartment of Kinesiology and Applied Physiology, University of Delaware, 540 S College Ave, Newark, DE 19713, USA.
Eric R MuñozDepartment of Kinesiology and Applied Physiology, University of Delaware, 540 S College Ave, Newark, DE 19713, USA.ORCID 0000-0003-0010-7513
Andrew D MitchellDepartment of Kinesiology and Applied Physiology, University of Delaware, 540 S College Ave, Newark, DE 19713, USA.
Joshua T SelsbyDepartment of Animal Science, Iowa State University, 2356G Kildee Hall, Ames, IA 50011, USA.
Matthew B HudsonDepartment of Kinesiology and Applied Physiology, University of Delaware, 540 S College Ave, Newark, DE 19713, USA.
University of Delaware · USIowa State University · US

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI Anjana Narayan Bhat · 2012 to 2026
$67.2M
Vascular Consequences of Duchenne Muscular DystrophyP20GM113125 · NIGMS · UNIVERSITY OF DELAWARE · PI SIONS, JACLYN MEGAN · 2016 to 2025
$23.3M
Behavioral- and bio-markers of subconcussion with controlled human head impactR01NS102157 · NINDS · UNIVERSITY OF DELAWARE · PI JEKA, JOHN JOSEPH, PARK, JOON YOUNG · 2017 to 2021
$3.2M
NIGMS NIH HHS P20 GM103446NIGMS NIH HHS P20 GM113125NINDS NIH HHS R01 NS102157
6 · The paper itself

Abstract

Muscle stem cells (MuSCs) hold great potential as a regenerative therapeutic but have met numerous challenges in treating systemic muscle diseases. Muscle stem cell-derived extracellular vesicles (MuSC-EVs) may overcome these limitations. We assessed the number and size distribution of extracellular vesicles (EVs) released by MuSCs ex vivo, determined the extent to which MuSC-EVs deliver molecular cargo to myotubes in vitro, and quantified MuSC-EV-mediated restoration of mitochondrial function following oxidative injury. MuSCs released an abundance of EVs in culture. MuSC-EVs delivered protein cargo into myotubes within 2 h of incubation. Fluorescent labeling of intracellular mitochondria showed co-localization of delivered protein and mitochondria. Oxidatively injured myotubes demonstrated a significant decline in maximal oxygen consumption rate and spare respiratory capacity relative to untreated myotubes. Remarkably, subsequent treatment with MuSC-EVs significantly improved maximal oxygen consumption rate and spare respiratory capacity relative to the myotubes that were damaged but received no subsequent treatment. Surprisingly, MuSC-EVs did not affect mitochondrial function in undamaged myotubes, suggesting the cargo delivered is able to repair but does not expand the existing mitochondrial network. These data demonstrate that MuSC-EVs rapidly deliver proteins into myotubes, a portion of which co-localizes with mitochondria, and reverses mitochondria dysfunction in oxidatively-damaged myotubes.

Indexed as

AnimalsExtracellular VesiclesFemaleHydrogen PeroxideMaleMiceMice, Inbred C57BLMitochondriaMitochondrial DiseasesMuscle Fibers, SkeletalMuscle, SkeletalMuscular DiseasesOxidative StressOxygen ConsumptionStem CellsHydrogen Peroxidecachexiaextracellular vesiclesmitochondriamuscle stem cellsmuscular dystrophyoxidative stressskeletal muscle

Identifiers

PMID33256005
PMCPMC7760380
OpenAlexW3110187286

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.