Evidence map›Paper›PMID 25229238›Full record

ArticlePloS one2014

New insights into the relationship between mIGF-1-induced hypertrophy and Ca2+ handling in differentiated satellite cells.

Simone Guarnieri, Caterina Morabito, Silvia Belia, Laura Barberi, Antonio Musarò, Giorgio Fanò-Illic, Maria A Mariggiò

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Evidence for Altered CaFrontiers in physiology · 2016
    Article
  3. Article
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 1 country.

Simone GuarnieriDepartment of Neuroscience Imaging and Clinical Sciences, StemTeCh group - CeSI, University G. d'Annunzio of Chieti-Pescara, Chieti, Italy; Interuniversity Institute of Myology (IIM), Italy.
Caterina MorabitoDepartment of Neuroscience Imaging and Clinical Sciences, StemTeCh group - CeSI, University G. d'Annunzio of Chieti-Pescara, Chieti, Italy; Interuniversity Institute of Myology (IIM), Italy.
Silvia BeliaDepartment of Cellular and Environmental Biology, University of Perugia, Perugia, Italy.
Laura BarberiInteruniversity Institute of Myology (IIM), Italy; Institute Pasteur Cenci-Bolognetti, DAHFMO - unit of Histology and Medical Embryology, Sapienza University of Rome, Rome, Italy.
Antonio MusaròInteruniversity Institute of Myology (IIM), Italy; Institute Pasteur Cenci-Bolognetti, DAHFMO - unit of Histology and Medical Embryology, Sapienza University of Rome, Rome, Italy; Center for Life Nano Science@Sapienza, Istituto Italiano di Tecnologia, Rome, Italy.
Giorgio Fanò-IllicDepartment of Neuroscience Imaging and Clinical Sciences, StemTeCh group - CeSI, University G. d'Annunzio of Chieti-Pescara, Chieti, Italy; Interuniversity Institute of Myology (IIM), Italy.
Maria A MariggiòDepartment of Neuroscience Imaging and Clinical Sciences, StemTeCh group - CeSI, University G. d'Annunzio of Chieti-Pescara, Chieti, Italy; Interuniversity Institute of Myology (IIM), Italy.
University of Chieti-Pescara · ITIstituto Pasteur · ITSapienza University of Rome · ITUniversity of Perugia · IT

Funding

Telethon GGP13013
6 · The paper itself

Abstract

Muscle regeneration involves the activation of satellite cells, is regulated at the genetic and epigenetic levels, and is strongly influenced by gene activation and environmental conditions. The aim of this study was to determine whether the overexpression of mIGF-1 can modify functional features of satellite cells during the differentiation process, particularly in relation to modifications of intracellular Ca2+ handling. Satellite cells were isolated from wild-type and MLC/mIGF-1 transgenic mice. The cells were differentiated in vitro, and morphological analyses, intracellular Ca2+ measurements, and ionic current recordings were performed. mIGF-1 overexpression accelerates satellite cell differentiation and promotes myotube hypertrophy. In addition, mIGF-1 overexpression-induced potentiation of myogenesis triggers both quantitative and qualitative changes to the control of intracellular Ca2+ handling. In particular, the differentiated MLC/mIGF-1 transgenic myotubes have reduced velocity and amplitude of intracellular Ca2+ increases after stimulation with caffeine, KCl and acetylcholine. This appears to be due, at least in part, to changes in the physico-chemical state of the sarcolemma (increased membrane lipid oxidation, increased output currents) and to increased expression of dihydropyridine voltage-operated Ca2+ channels. Interestingly, extracellular ATP and GTP evoke intracellular Ca2+ mobilization to greater extents in the MLC/mIGF-1 transgenic satellite cells, compared to the wild-type cells. These data suggest that these MLC/mIGF-1 transgenic satellite cells are more sensitive to trophic stimuli, which can potentiate the effects of mIGF-1 on the myogenic programme.

Indexed as

Cell DifferentiationAnimalsCalciumElectrophysiological PhenomenaExtracellular SpaceHomeostasisHypertrophyInsulin-Like Growth Factor IMembrane FluidityMiceMice, TransgenicMuscle Fibers, SkeletalMyosin Light ChainsOxidative StressSatellite Cells, Skeletal MuscleCalciumInsulin-Like Growth Factor IMyosin Light Chains

Identifiers

PMID25229238
PMCPMC4168228
OpenAlexW2037284342

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.