Evidence map›Paper›PMID 26431586›Full record

ArticleExperimental cell research2015

PKCε as a novel promoter of skeletal muscle differentiation and regeneration.

D Di Marcantonio, D Galli, C Carubbi, G Gobbi, V Queirolo, S Martini, S Merighi, M Vaccarezza, N Maffulli, S M Sykes and 2 more

Open access · greenAbstract read
In one paragraph

Article in Experimental cell research, 2015. 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
1.1field-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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  4. Article
  5. Article
  6. Review
  7. HMGA Genes and Proteins in Development and Evolution.International journal of molecular sciences · 2020
    Review
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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

12 authors at 5 institutions in 4 countries.

D Di MarcantonioDepartment of Biomedical, Biotechnological and Translational Sciences (S.Bi.Bi.T.), University of Parma, Via Gramsci, 14, 43100 Parma, Italy; Immune Cell Development and Host Defense, Research Institute of Fox Chase Cancer Center, Philadelphia, PA, USA.
D GalliDepartment of Biomedical, Biotechnological and Translational Sciences (S.Bi.Bi.T.), University of Parma, Via Gramsci, 14, 43100 Parma, Italy; Centre for Molecular and Translational Oncology (COMT), University of Parma, Italy; Sport and Exercise Medicine Center (SEM), University of Parma, Italy.
C CarubbiDepartment of Biomedical, Biotechnological and Translational Sciences (S.Bi.Bi.T.), University of Parma, Via Gramsci, 14, 43100 Parma, Italy.
G GobbiDepartment of Biomedical, Biotechnological and Translational Sciences (S.Bi.Bi.T.), University of Parma, Via Gramsci, 14, 43100 Parma, Italy; Centre for Molecular and Translational Oncology (COMT), University of Parma, Italy; Sport and Exercise Medicine Center (SEM), University of Parma, Italy.
V QueiroloDepartment of Biomedical, Biotechnological and Translational Sciences (S.Bi.Bi.T.), University of Parma, Via Gramsci, 14, 43100 Parma, Italy.
S MartiniDepartment of Biomedical, Biotechnological and Translational Sciences (S.Bi.Bi.T.), University of Parma, Via Gramsci, 14, 43100 Parma, Italy.
S MerighiDepartment of Medical Science, University of Ferrara, Italy.
M VaccarezzaDepartment of Human Sciences, Society and Health (HSSH), University of Cassino, FR, Italy; School of Biomedical Sciences, University of Queensland, Brisbane, QLD 4072, Australia.
N MaffulliBarts and The London School of Medicine and Dentistry, Queen Mary University of London, UK; Department of Musculoskeletal Disorders, University of Salerno School of Medicine and Surgery, Salerno, Italy.
S M SykesImmune Cell Development and Host Defense, Research Institute of Fox Chase Cancer Center, Philadelphia, PA, USA.
M VitaleDepartment of Biomedical, Biotechnological and Translational Sciences (S.Bi.Bi.T.), University of Parma, Via Gramsci, 14, 43100 Parma, Italy; Centre for Molecular and Translational Oncology (COMT), University of Parma, Italy; Sport and Exercise Medicine Center (SEM), University of Parma, Italy. Electronic address: marco.vitale@unipr.it.
P MirandolaDepartment of Biomedical, Biotechnological and Translational Sciences (S.Bi.Bi.T.), University of Parma, Via Gramsci, 14, 43100 Parma, Italy; Centre for Molecular and Translational Oncology (COMT), University of Parma, Italy; Sport and Exercise Medicine Center (SEM), University of Parma, Italy.
University of Parma · ITFox Chase Cancer Center · USUniversity of Ferrara · ITUniversity of Queensland · AUUniversity of Salerno · IT

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
NCI NIH HHS P30 CA006927
6 · The paper itself

Abstract

introductionSatellite cells are muscle resident stem cells and are responsible for muscle regeneration. In this study we investigate the involvement of PKCε during muscle stem cell differentiation in vitro and in vivo. Here, we describe the identification of a previously unrecognized role for the PKCε-HMGA1 signaling axis in myoblast differentiation and regeneration processes.

methodsPKCε expression was modulated in the C2C12 cell line and primary murine satellite cells in vitro, as well as in an in vivo model of muscle regeneration. Immunohistochemistry and immunofluorescence, RT-PCR and shRNA silencing techniques were used to determine the role of PKCε and HMGA1 in myogenic differentiation.

resultsPKCε expression increases and subsequently re-localizes to the nucleus during skeletal muscle cell differentiation. In the nucleus, PKCε blocks Hmga1 expression to promote Myogenin and Mrf4 accumulation and myoblast formation. Following in vivo muscle injury, PKCε accumulates in regenerating, centrally-nucleated myofibers. Pharmacological inhibition of PKCε impairs the expression of two crucial markers of muscle differentiation, namely MyoD and Myogenin, during injury induced muscle regeneration.

conclusionThis work identifies the PKCε-HMGA1 signaling axis as a positive regulator of skeletal muscle differentiation.

Indexed as

Cell DifferentiationAnimalsBlotting, WesternCells, CulturedFluorescent Antibody TechniqueHMGA1a ProteinImmunoenzyme TechniquesMiceMuscle DevelopmentMuscle, SkeletalMyoblastsProtein Kinase C-epsilonReal-Time Polymerase Chain ReactionRegenerationReverse Transcriptase Polymerase Chain ReactionRNA, MessengerHMGA1a ProteinProtein Kinase C-epsilonRNA, MessengerRNA, Small InterferingC2C12HMGA1PKCεSatellite cellsSkeletal muscle differentiation

Identifiers

PMID26431586
PMCPMC5130411
OpenAlexW1822303284

What OpenQuestion holds

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Registered trials

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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.