Evidence map›Paper›PMID 26771351›Full record

ArticleStem cell reports2016

Development of Bipotent Cardiac/Skeletal Myogenic Progenitors from MESP1+ Mesoderm.

Sunny Sun-Kin Chan, Hannah R Hagen, Scott A Swanson, Ron Stewart, Karly A Boll, Joy Aho, James A Thomson, Michael Kyba

Abstract read
In one paragraph

Article in Stem cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Cardiac commitment driven by MyoD expression in pericardial stem cells.Frontiers in cell and developmental biology · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. The TGFβ superfamily in cardiac dysfunction.Acta biochimica et biophysica Sinica · 2018
    Review
  19. Article
  20. Myogenic progenitor specification from pluripotent stem cells.Seminars in cell & developmental biology · 2017
    Review
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

8 authors.

Sunny Sun-Kin ChanLillehei Heart Institute, University of Minnesota, Minneapolis, MN 55455, USA; Department of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.
Hannah R HagenLillehei Heart Institute, University of Minnesota, Minneapolis, MN 55455, USA.
Scott A SwansonMorgridge Institute for Research, University of Wisconsin-Madison, Madison, WI 53715, USA.
Ron StewartMorgridge Institute for Research, University of Wisconsin-Madison, Madison, WI 53715, USA.
Karly A BollLillehei Heart Institute, University of Minnesota, Minneapolis, MN 55455, USA.
Joy AhoStem Cells Department, R&D Systems, Inc., Minneapolis, MN 55413, USA.
James A ThomsonMorgridge Institute for Research, University of Wisconsin-Madison, Madison, WI 53715, USA.
Michael KybaDepartment of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA; Lillehei Heart Institute, University of Minnesota, Cancer and Cardiovascular Research Building 4-127, 2231 6th Street Southeast, Minneapolis, MN 55455, USA. Electronic address: kyba@umn.edu.

Funding

Midwestern Progenitor Cell ConsortiumU01HL100407 · NHLBI · UNIVERSITY OF MINNESOTA · PI GARRY, DANIEL J., KYBA, MICHAEL · 2009 to 2015
$7.8M
Use of specific transcription factors to promote limb regeneration capacityP30AR057220 · NIAMS · UNIVERSITY OF MINNESOTA · PI DARABI, RADBOD · 2009 to 2013
$3.0M
NHLBI NIH HHS U01 HL100407NIAMS NIH HHS P30 AR057220
6 · The paper itself

Abstract

The branchiomeric skeletal muscles co-evolved with new chambers of the heart to enable predatory feeding in chordates. These co-evolved tissues develop from a common population in anterior splanchnic mesoderm, referred to as cardiopharyngeal mesoderm (CPM). The regulation and development of CPM are poorly understood. We describe an embryonic stem cell-based system in which MESP1 drives a PDGFRA+ population with dual cardiac and skeletal muscle differentiation potential, and gene expression resembling CPM. Using this system, we investigate the regulation of these bipotent progenitors, and find that cardiac specification is governed by an antagonistic TGFβ-BMP axis, while skeletal muscle specification is enhanced by Rho kinase inhibition. We define transcriptional signatures of the first committed CPM-derived cardiac and skeletal myogenic progenitors, and discover surface markers to distinguish cardiac (PODXL+) from the skeletal muscle (CDH4+) CPM derivatives. These tools open an accessible window on this developmentally and evolutionarily important population.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCadherinsCell DifferentiationCells, CulturedGene Expression ProfilingGene Expression Regulation, DevelopmentalImmunohistochemistryMesodermMiceMouse Embryonic Stem CellsMuscle DevelopmentMuscle, SkeletalMyocardiumPluripotent Stem CellsReceptor, Platelet-Derived Growth Factor alphaBasic Helix-Loop-Helix ProteinsCadherinsMesp1 protein, mousepodocalyxinR-cadherinReceptor, Platelet-Derived Growth Factor alphaSialoglycoproteinscardiac developmentcardiopharyngeal mesodermmesodermMesp1skeletal myogenesis

Identifiers

PMID26771351
PMCPMC4719188

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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.