Evidence map›Paper›PMID 38466320›Full record

ArticleeLife2024

A novel imaging method (FIM-ID) reveals that myofibrillogenesis plays a major role in the mechanically induced growth of skeletal muscle.

Kent W Jorgenson, Jamie E Hibbert, Ramy K A Sayed, Anthony N Lange, Joshua S Godwin, Paulo H C Mesquita, Bradley A Ruple, Mason C McIntosh, Andreas N Kavazis, Michael D Roberts and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 6 citations in OpenAlex.

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  10. Aberrant evoked calcium signaling and nAChR cluster morphology in aFrontiers in cell and developmental biology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 2 countries.

Kent W JorgensonSchool of Veterinary Medicine and the Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, United States.ORCID https://orcid.org/0000-0001-5206-8507
Jamie E HibbertSchool of Veterinary Medicine and the Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, United States.ORCID https://orcid.org/0000-0001-7327-6460
Ramy K A SayedSchool of Veterinary Medicine and the Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, United States.ORCID https://orcid.org/0000-0003-4467-6742
Anthony N LangeSchool of Veterinary Medicine and the Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, United States.
Joshua S GodwinSchool of Kinesiology, Auburn University, Auburn, United States.
Paulo H C MesquitaSchool of Kinesiology, Auburn University, Auburn, United States.
Bradley A RupleSchool of Kinesiology, Auburn University, Auburn, United States.
Mason C McIntoshSchool of Kinesiology, Auburn University, Auburn, United States.
Andreas N KavazisSchool of Kinesiology, Auburn University, Auburn, United States.
Michael D RobertsSchool of Kinesiology, Auburn University, Auburn, United States.
Troy A HornbergerSchool of Veterinary Medicine and the Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, United States.ORCID https://orcid.org/0000-0002-2349-1899
University of Wisconsin–Madison · US

Funding

The Role of TRIM28 Phosphorylation in the Mechanical Regulation of Skeletal Muscle - Re-entry SupplementR01AR074932 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI HORNBERGER, TROY A · 2020 to 2024
$2.0M
Identifying the Structural Adaptations that Drive the Mechanically Induced Growth of Skeletal MuscleR01AR082816 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI TROY A HORNBERGER · 2023 to 2026
$1.9M
G-RISE at Auburn UniversityT32GM141739 · NIGMS · AUBURN UNIVERSITY AT AUBURN · PI CLAYTON, TAFFYE BENSON, RUSSELL, MELODY L · 2021 to 2024
$1.2M
NIAMS NIH HHS AR074932NIAMS NIH HHS AR082816NIAMS NIH HHS R01 AR074932NIAMS NIH HHS R01 AR082816NIGMS NIH HHS GM141739NIGMS NIH HHS T32 GM141739
6 · The paper itself

Abstract

An increase in mechanical loading, such as that which occurs during resistance exercise, induces radial growth of muscle fibers (i.e. an increase in cross-sectional area). Muscle fibers are largely composed of myofibrils, but whether radial growth is mediated by an increase in the size of the myofibrils (i.e. myofibril hypertrophy) and/or the number of myofibrils (i.e. myofibrillogenesis) is not known. Electron microscopy (EM) can provide images with the level of resolution that is needed to address this question, but the acquisition and subsequent analysis of EM images is a time- and cost-intensive process. To overcome this, we developed a novel method for visualizing myofibrils with a standard fluorescence microscope (fluorescence imaging of myofibrils with image deconvolution [FIM-ID]). Images from FIM-ID have a high degree of resolution and contrast, and these properties enabled us to develop pipelines for automated measurements of myofibril size and number. After extensively validating the automated measurements, we used both mouse and human models of increased mechanical loading to discover that the radial growth of muscle fibers is largely mediated by myofibrillogenesis. Collectively, the outcomes of this study offer insight into a fundamentally important topic in the field of muscle growth and provide future investigators with a time- and cost-effective means to study it.

Indexed as

Muscle, SkeletalMyofibrilsAnimalsHumansHypertrophyMiceMuscle Fibers, SkeletalOptical Imagingcell biologyexercisegrowthhypertrophymousemyofibrilskeletal muscleultrastructure

Identifiers

PMID38466320
PMCPMC10928493
OpenAlexW4388971932

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.