Evidence map›Paper›PMID 28410244›Full record

ArticleOncotarget2017

Platelet-derived growth factor receptor-alpha positive cardiac progenitor cells derived from multipotent germline stem cells are capable of cardiomyogenesis in vitro and in vivo.

Bang-Jin Kim, Yong-Hee Kim, Yong-An Lee, Sang-Eun Jung, Yeong Ho Hong, Eun-Ju Lee, Byung-Gak Kim, Seongsoo Hwang, Jeong Tae Do, Myung-Geol Pang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. PdgfrαGenes & diseases · 2025
    Review
  5. Article
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  7. Article
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  10. Platelet-derived growth factor receptor-α is essential for cardiac fibroblast survival.American journal of physiology. Heart and circulatory physiology · 2019
    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

11 authors at 6 institutions in 3 countries.

Bang-Jin KimDepartment of Animal Science & Technology, Chung-Ang University, Anseong, Republic of Korea.
Yong-Hee KimDepartment of Animal Science & Technology, Chung-Ang University, Anseong, Republic of Korea.
Yong-An LeeLaboratory of Bioimaging Probe Development, Singapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Sang-Eun JungDepartment of Animal Science & Technology, Chung-Ang University, Anseong, Republic of Korea.
Yeong Ho HongDepartment of Animal Science & Technology, Chung-Ang University, Anseong, Republic of Korea.
Eun-Ju LeeDepartment of Internal medicine, Seoul National University, Seoul, Republic of Korea.
Byung-Gak KimBio Environment Technology Research Institute, Chung-Ang University, Anseong, Republic of Korea.
Seongsoo HwangAnimal Biotechnology Division, National Institute of Animal Science, Jeollabuk-do, Republic of Korea.
Jeong Tae DoDepartment of Stem Cell and Regenerative Biology, College of Animal Bioscience and Technology, Konkuk University, Seoul, Republic of Korea.
Myung-Geol PangDepartment of Animal Science & Technology, Chung-Ang University, Anseong, Republic of Korea.
Buom-Yong RyuDepartment of Animal Science & Technology, Chung-Ang University, Anseong, Republic of Korea.
Chung-Ang University · KRAgency for Science, Technology and Research · SGKonkuk University · KRNational Institute of Animal Science · KRSeoul National University · KRUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac cell therapy has the potential to revolutionize treatment of heart diseases, but its success hinders on the development of a stem cell therapy capable of efficiently producing functionally differentiated cardiomyocytes. A key to unlocking the therapeutic application of stem cells lies in understanding the molecular mechanisms that govern the differentiation process. Here we report that a population of platelet-derived growth factor receptor alpha (PDGFRA) cells derived from mouse multipotent germline stem cells (mGSCs) were capable of undergoing cardiomyogenesis in vitro. Cells derived in vitro from PDGFRA positive mGSCs express significantly higher levels of cardiac marker proteins compared to PDGFRA negative mGSCs. Using Pdgfra shRNAs to investigate the dependence of Pdgfra on cardiomyocyte differentiation, we observed that Pdgfra silencing inhibited cardiac differentiation. In a rat myocardial infarction (MI) model, transplantation of a PDGFRAenriched cell population into the rat heart readily underwent functional differentiation into cardiomyocytes and reduced areas of fibrosis associated with MI injury. Together, these results suggest that mGSCs may provide a unique source of cardiac stem/progenitor cells for future regenerative therapy of damaged heart tissue.

Indexed as

Cell DifferentiationAnimalsBone Morphogenetic Protein 4Cell Culture TechniquesCell LineageCells, CulturedCell Transformation, NeoplasticDisease Models, AnimalGene ExpressionGene Knockout TechniquesGerm CellsMiceMultipotent Stem CellsMyoblasts, CardiacMyocardial InfarctionMyocytes, CardiacBone Morphogenetic Protein 4Receptor, Platelet-Derived Growth Factor alphacardiac progenitordifferentiationgerm-line stem cellsmultipotenttestis

Identifiers

PMID28410244
PMCPMC5444692
OpenAlexW2598194131

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.