Evidence map›Paper›PMID 31719871›Full record

ArticleCellular and molecular bioengineering2017

Data-Modeling Identifies Conflicting Signaling Axes Governing Myoblast Proliferation and Differentiation Responses to Diverse Ligand Stimuli.

Alexander M Loiben, Sharon Soueid-Baumgarten, Ruth F Kopyto, Debadrita Bhattacharya, Joseph C Kim, Benjamin D Cosgrove

Open access · bronzeAbstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2017. 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
0.3field-weighted citation impact, top 39% 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, 7 citations in OpenAlex.

  1. 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

6 authors at 1 institution in 1 country.

Alexander M Loiben1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853 USA.ORCID 0000-0001-7782-0726
Sharon Soueid-Baumgarten1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853 USA.ORCID 0000-0001-6875-7841
Ruth F Kopyto2Biological Sciences, College of Agriculture and Life Sciences, Cornell University, Ithaca, NY 14853 USA.ORCID 0000-0003-3617-7302
Debadrita Bhattacharya3Graduate Field of Biochemistry, Molecular and Cell Biology, Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853 USA.ORCID 0000-0002-1923-2675
Joseph C Kim1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853 USA.ORCID 0000-0002-6305-4554
Benjamin D Cosgrove1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853 USA.ORCID 0000-0003-2164-350X
Cornell University · US

Funding

Supplement to: EX VIVO REJUVENATION AND EXPANSION OF MUSCLE STEM CELLS FROM AGED MICER00AG042491 · NIA · CORNELL UNIVERSITY · PI COSGROVE, BENJAMIN DAVID · 2014 to 2016
$790k
NIA NIH HHS R00 AG042491
6 · The paper itself

Abstract

introductionSkeletal muscle tissue development and regeneration relies on the proliferation, maturation and fusion of muscle progenitor cells (myoblasts), which arise transiently from muscle stem cells (satellite cells). Following muscle damage, myoblasts proliferate and differentiate in response to temporally-varying inflammatory cytokines, growth factors, and extracellular matrix cues, which stimulate a shared network of intracellular signaling pathways. Here we present an integrated data-modeling approach to elucidate synergies and antagonisms among proliferation and differentiation signaling axes in myoblasts stimulated by regeneration-associated ligands.

methodsWe treated mouse primary myoblasts in culture with combinations of eight regeneration-associated growth factors and cytokines in mixtures that induced additive, synergistic, and antagonistic effects on myoblast proliferation and differentiation responses. For these combinatorial stimuli, we measured the activation dynamics of seven signal transduction pathways using multiplexed phosphoprotein assays and scored proliferation and differentiation responses based on expression of myogenic commitment factors to assemble a cue-signaling-response data compendium. We interrogated the relationship between these signals and responses by partial least-squares (PLS) regression modeling.

resultsPartial least-squares data-modeling accurately predicted response outcomes in cross-validation on the training compendium (cumulative

conclusionThis data-modeling approach identified conflicting signaling axes that underlie muscle progenitor cell proliferation and differentiation.

Indexed as

Cue-signal-response modelingCytokinesGrowth factorsPartial least-squares regressionSkeletal muscleSystems biology

Identifiers

PMID31719871
PMCPMC6816730
OpenAlexW2756307233

What OpenQuestion holds

Textmetadata
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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.