Evidence map›Paper›PMID 30206294›Full record

ArticleScientific reports2018

Zinc uptake promotes myoblast differentiation via Zip7 transporter and activation of Akt signalling transduction pathway.

Hayk Mnatsakanyan, Roser Sabater I Serra, Patricia Rico, Manuel Salmerón-Sánchez

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  6. Zinc Depletion Increases Susceptibility to AMPK-Induced Atrophic Responses in C2C12 Myotubes.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Article
  7. Zinc deficiency contributes to blunted myogenesis in chronic kidney disease.American journal of physiology. Cell physiology · 2026
    Article
  8. Review
  9. SLC39A8-mediated zinc dyshomeostasis potentiates kidney disease.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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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

4 authors at 2 institutions in 2 countries.

Hayk MnatsakanyanCentre for Biomaterials and Tissue Engineering (CBIT) Universitat Politècnica de València, 46022, Valencia, Spain.
Roser Sabater I SerraCentre for Biomaterials and Tissue Engineering (CBIT) Universitat Politècnica de València, 46022, Valencia, Spain.ORCID 0000-0002-5550-7066
Patricia RicoCentre for Biomaterials and Tissue Engineering (CBIT) Universitat Politècnica de València, 46022, Valencia, Spain. parico@upvnet.upv.es.
Manuel Salmerón-SánchezCentre for Biomaterials and Tissue Engineering (CBIT) Universitat Politècnica de València, 46022, Valencia, Spain. manuel.salmeron-sanchez@glasgow.ac.uk.
Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine · ESUniversitat Politècnica de València · ES

Funding

EC | European Research Council (ERC) ERC - HealInSynergy 306990Engineering and Physical Sciences Research Council (EPSRC) EPSRC - EP/P001114/1
6 · The paper itself

Abstract

Myogenic regeneration occurs through a chain of events beginning with the output of satellite cells from quiescent state, formation of competent myoblasts and later fusion and differentiation into myofibres. Traditionally, growth factors are used to stimulate muscle regeneration but this involves serious off-target effects, including alterations in cell homeostasis and cancer. In this work, we have studied the use of zinc to trigger myogenic differentiation. We show that zinc promotes myoblast proliferation, differentiation and maturation of myofibres. We demonstrate that this process occurs through the PI3K/Akt pathway, via zinc stimulation of transporter Zip7. Depletion of zinc transporter Zip7 by RNA interference shows reduction of both PI3K/Akt signalling and a significant reduction of multinucleated myofibres and myotubes development. Moreover, we show that mature myofibres, obtained through stimulation with high concentrations of zinc, accumulate zinc and so we hypothesise their function as zinc reservoirs into the cell.

Indexed as

AnimalsCation Transport ProteinsCell DifferentiationCell ProliferationGene Expression Regulation, DevelopmentalMiceMuscle DevelopmentMuscle, SkeletalMyoblastsOncogene Protein v-aktPhosphorylationRegenerationZincCation Transport ProteinsOncogene Protein v-aktSlc39a7 protein, mouseZinc

Identifiers

PMID30206294
PMCPMC6133932
OpenAlexW2890864585

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.