Evidence map›Paper›PMID 32381068›Full record

ArticleSkeletal muscle2020

Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue.

Robert Louis Hastings, Ryan T Massopust, Seth G Haddix, Young Il Lee, Wesley J Thompson

Open access · goldAbstract read
In one paragraph

Article in Skeletal muscle, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Robert Louis HastingsTexas A&M Institute for Neuroscience, College Station, TX, USA. robertlouishastings@gmail.com.ORCID 0000-0003-3342-7441
Ryan T MassopustTexas A&M Institute for Neuroscience, College Station, TX, USA.
Seth G HaddixTexas A&M Institute for Neuroscience, College Station, TX, USA.
Young Il LeeDepartment of Biology, Texas A&M University, College Station, TX, USA.
Wesley J ThompsonTexas A&M Institute for Neuroscience, College Station, TX, USA.
Texas A&M University · US

Funding

SYNAPSE ELIMINATION IN NEONATAL SKELETAL MUSCLER01NS020480 · NINDS · UNIVERSITY OF TEXAS AUSTIN · PI MCMAHAN, UEL J · 1985 to 2019
$2.8M
NINDS NIH HHS R01 NS020480
6 · The paper itself

Abstract

backgroundThe arrangement of myonuclei in skeletal muscle tissue has long been used as a biomarker for muscle health, but there is a dearth of in vivo exploration of potential effects of myonuclear organization on the function and regeneration of skeletal muscle because traditional nuclear stains are performed on postmortem tissue. Therefore, we sought a transgenic method to produce a selective and persistent myonuclear label in whole muscles of living mice.

methodsWe bred together a mouse line with skeletal muscle fiber-selective expression of Cre recombinase and a second mouse line with a Cre-inducible fluorescently tagged histone protein to generate a mouse line that produces a myonuclear label suitable for vital imaging and histology of fixed tissue. We tested the effectiveness of this vital label in three conditions known to generate abnormal myonuclear positioning. First, we injured myofibers of young mice with cardiotoxin. Second, this nuclear label was bred into a murine model of Duchenne muscular dystrophy. Finally, we examined old mice from this line that have undergone the natural aging process. Welch's t test was used to compare wild type and transgenic mice.

resultsThe resulting mouse line transgenically produces a vital red fluorescent label of myonuclei, which facilitates their in vivo imaging in skeletal muscle tissue. Transgenic fluorescent labeling of myonuclei has no significant effect on skeletal muscle function, as determined by twitch and tetanic force recordings. In each muscle examined, including those under damaged, dystrophic, and aged conditions, the labeled myonuclei exhibit morphology consistent with established literature, and reveal a specialized arrangement of subsynaptic myonuclei at the neuromuscular junction.

conclusionsTaken together, our results demonstrate that this mouse line provides a versatile tool to selectively visualize myonuclei within both living and fixed preparations of healthy, injured, diseased, and aged muscles.

Indexed as

Cell FusionAgingAnimalsCardiotoxinsCell NucleusCells, CulturedFemaleHistonesLuminescent ProteinsMaleMiceMice, Inbred C57BLMice, Inbred mdxMuscle Fibers, SkeletalMuscular Dystrophy, DuchenneRecombinant ProteinsCardiotoxinsHistonesLuminescent ProteinsRecombinant ProteinsRed Fluorescent ProteinCentral nucleiHistone H2BHSAHuman skeletal actinmdxRGSoleplate nuclei

Identifiers

PMID32381068
PMCPMC7204059
OpenAlexW3023570602

What OpenQuestion holds

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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.