Evidence map›Paper›PMID 24647690›Full record

ArticlePloS one2014

Pro-inflammatory mediation of myoblast proliferation.

Jeffrey S Otis, Sarah Niccoli, Nicole Hawdon, Jessica L Sarvas, Melinda A Frye, Adam J Chicco, Simon J Lees

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

57 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
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  4. FAPs orchestrate homeostasis of muscle physiology and pathophysiology.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Review
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  17. Continuous Oral Administration of SonicatedInternational journal of environmental research and public health · 2022
    Article
  18. Article
  19. Review
  20. 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

7 authors at 4 institutions in 2 countries.

Jeffrey S OtisDepartment of Kinesiology and Health, Georgia State University, Atlanta, Georgia, United States of America.
Sarah NiccoliMedical Sciences Division, Northern Ontario School of Medicine, Thunder Bay, Ontario, Canada.
Nicole HawdonMedical Sciences Division, Northern Ontario School of Medicine, Thunder Bay, Ontario, Canada.
Jessica L SarvasMedical Sciences Division, Northern Ontario School of Medicine, Thunder Bay, Ontario, Canada; Department of Biology, Lakehead University, Thunder Bay, Ontario, Canada.
Melinda A FryeDepartment of Biomedical Sciences, Colorado State University, Fort Collins, Colorado, United States of America.
Adam J ChiccoDepartment of Health and Exercise Science, Colorado State University, Fort Collins, Colorado, United States of America.
Simon J LeesMedical Sciences Division, Northern Ontario School of Medicine, Thunder Bay, Ontario, Canada; Department of Biology, Lakehead University, Thunder Bay, Ontario, Canada; Department of Health and Exercise Science, Colorado State University, Fort Collins, Colorado, United States of America.
NOSM University · CAColorado State University · USGeorgia State University · USLakehead University · CA

Funding

Age-environment interaction influencing skeletal muscle satellite cell functionR03AG034352 · NIA · COLORADO STATE UNIVERSITY · PI LEES, SIMON JAMES · 2011 to 2012
$112k
NIA NIH HHS R03 AG-034352NIA NIH HHS R03 AG034352PHS HHS K01 017190
6 · The paper itself

Abstract

Skeletal muscle satellite cell function is largely dictated by the surrounding environment following injury. Immune cell infiltration dominates the extracellular space in the injured area, resulting in increased cytokine concentrations. While increased pro-inflammatory cytokine expression has been previously established in the first 3 days following injury, less is known about the time course of cytokine expression and the specific mechanisms of cytokine induced myoblast function. Therefore, the expression of IL-1β and IL-6 at several time points following injury, and their effects on myoblast proliferation, were examined. In order to do this, skeletal muscle was injured using barium chloride in mice and tissue was collected 1, 5, 10, and 28 days following injury. Mechanisms of cytokine induced proliferation were determined in cell culture using both primary and C2C12 myoblasts. It was found that there is a ∼20-fold increase in IL-1β (p≤0.05) and IL-6 (p = 0.06) expression 5 days following injury. IL-1β increased proliferation of both primary and C2C12 cells ∼25%. IL-1β stimulation also resulted in increased NF-κB activity, likely contributing to the increased proliferation. These data demonstrate for the first time that IL-1β alone can increase the mitogenic activity of primary skeletal muscle satellite cells and offer insight into the mechanisms dictating satellite cell function following injury.

Indexed as

AnimalsCell LineCell ProliferationCells, CulturedInterleukin-1betaInterleukin-6MaleMiceMyoblastsRatsReverse Transcriptase Polymerase Chain ReactionTumor Necrosis Factor-alphaInterleukin-1betaInterleukin-6Tumor Necrosis Factor-alpha

Identifiers

PMID24647690
PMCPMC3960233
OpenAlexW2083028088

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.