Evidence map›Paper›PMID 25109702›Full record

ArticleAging2014

Mechanisms of action of hESC-secreted proteins that enhance human and mouse myogenesis.

Hanadie Yousef, Michael J Conboy, Hikaru Mamiya, Matthew Zeiderman, Christina Schlesinger, David V Schaffer, Irina M Conboy

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Current Thoughts of Notch's Role in Myoblast Regulation and Muscle-Associated Disease.International journal of environmental research and public health · 2021
    Review
  3. Article
  4. Article
  5. Article
  6. Rotator cuff tear state modulates self-renewal and differentiation capacity of human skeletal muscle progenitor cells.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2017
    Article
  7. Review
  8. 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 2 institutions in 1 country.

Hanadie YousefDepartment of Molecular and Cellular Biology, UC Berkeley, Berkeley, CA 94720, USA. co-first authors.
Michael J ConboyDepartment of Bioengineering and California Institute for Quantitative Biosciences (QB3), UC Berkeley, Berkeley, CA 94720, USA. co-first authors.
Hikaru MamiyaDepartment of Bioengineering and California Institute for Quantitative Biosciences (QB3), UC Berkeley, Berkeley, CA 94720, USA.
Matthew ZeidermanDepartment of Molecular and Cellular Biology, UC Berkeley, Berkeley, CA 94720, USA.
Christina SchlesingerDepartment of Bioengineering and California Institute for Quantitative Biosciences (QB3), UC Berkeley, Berkeley, CA 94720, USA.
David V SchafferDepartment of Bioengineering and California Institute for Quantitative Biosciences (QB3), UC Berkeley, Berkeley, CA 94720, USA. Department of Chemical and Biomolecular Engineering and Helen Wills Neuroscience Institute, UC Berkeley, Berkeley, CA 94720 USA.
Irina M ConboyDepartment of Bioengineering and California Institute for Quantitative Biosciences (QB3), UC Berkeley, Berkeley, CA 94720, USA.
University of California, Berkeley · USQB3 · US

Funding

Univ of Calif Berkeley Chemistry-Biology Interface ProgramT32GM066698 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI CHANG, CHRISTOPHER J., FRANCIS, MATTHEW B · 2004 to 2023
$7.5M
NIA NIH HHS R01 AG02725201NIGMS NIH HHS T32 GM066698
6 · The paper itself

Abstract

Adult stem cells grow poorly in vitro compared to embryonic stem cells, and in vivo stem cell maintenance and proliferation by tissue niches progressively deteriorates with age. We previously reported that factors produced by human embryonic stem cells (hESCs) support a robust regenerative capacity for adult and old mouse muscle stem/progenitor cells. Here we extend these findings to human muscle progenitors and investigate underlying molecular mechanisms. Our results demonstrate that hESC-conditioned medium enhanced the proliferation of mouse and human muscle progenitors. Furthermore, hESC-produced factors activated MAPK and Notch signaling in human myogenic progenitors, and Delta/Notch-1 activation was dependent on MAPK/pERK. The Wnt, TGF-β and BMP/pSmad1,5,8 pathways were unresponsive to hESC-produced factors, but BMP signaling was dependent on intact MAPK/pERK. c-Myc, p57, and p18 were key effectors of the enhanced myogenesis promoted by the hECS factors. To define some of the active ingredients of the hESC-secretome which may have therapeutic potential, a comparative proteomic antibody array analysis was performed and identified several putative proteins, including FGF2, 6 and 19 which as ligands for MAPK signaling, were investigated in more detail. These studies emphasize that a "youthful" signaling of multiple signaling pathways is responsible for the pro-regenerative activity of the hESC factors.

Indexed as

AnimalsCulture Media, ConditionedEmbryonic Stem CellsHumansIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiceMuscle DevelopmentReceptor, Notch1Signal TransductionTransforming Growth Factor betaCulture Media, Conditioneddelta proteinIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptor, Notch1Transforming Growth Factor beta

Identifiers

PMID25109702
PMCPMC4169857
OpenAlexW3590519

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.