Evidence map›Paper›PMID 26474484›Full record

ArticlePloS one2015

C-Kit Promotes Growth and Migration of Human Cardiac Progenitor Cells via the PI3K-AKT and MEK-ERK Pathways.

Bathri N Vajravelu, Kyung U Hong, Tareq Al-Maqtari, Pengxiao Cao, Matthew C L Keith, Marcin Wysoczynski, John Zhao, Joseph B Moore, Roberto Bolli

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Ex Vivo Expansion and Homing of Human Cord Blood Hematopoietic Stem Cells.Advances in experimental medicine and biology · 2023
    Article
  10. Article
  11. Article
  12. 'Youthful' phenotype of c-KitCellular and molecular life sciences : CMLS · 2022
    Article
  13. Article
  14. Article
  15. Review
  16. Cardiotoxic effects of angiogenesis inhibitors.Clinical science (London, England : 1979) · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. Human CardioChimeras: Creation of a Novel "Next-Generation" Cardiac Cell.Journal of the American Heart Association · 2020
    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

9 authors at 1 institution in 1 country.

Bathri N VajraveluInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
Kyung U HongInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
Tareq Al-MaqtariInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
Pengxiao CaoInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
Matthew C L KeithInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
Marcin WysoczynskiInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
John ZhaoInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
Joseph B MooreInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
Roberto BolliInstitute of Molecular Cardiology, Department of Medicine, University of Louisville, Louisville, KY 40202, United States of America.
University of Louisville · US

Funding

Tumor Necrosis Factor Modulation of CPCsP01HL078825 · NHLBI · UNIVERSITY OF LOUISVILLE · PI BOLLI, ROBERTO · 2005 to 2021
$37.6M
Project 5 - Metabolomic Analysis of AtherothrombosisP20GM103492 · NIGMS · UNIVERSITY OF LOUISVILLE · PI DEFILIPPIS, ANDREW · 2012 to 2017
$13.8M
University of Louisville Regional Clinical Center for the CCTRNUM1HL113530 · NHLBI · UNIVERSITY OF LOUISVILLE · PI BOLLI, ROBERTO · 2012 to 2018
$2.9M
NHLBI NIH HHS P01 HL078825NHLBI NIH HHS UM1 HL113530NIGMS NIH HHS P20 GM103492
6 · The paper itself

Abstract

A recent phase I clinical trial (SCIPIO) has shown that autologous c-kit+ cardiac progenitor cells (CPCs) improve cardiac function and quality of life when transplanted into patients with ischemic heart disease. Although c-kit is widely used as a marker of resident CPCs, its role in the regulation of the cellular characteristics of CPCs remains unknown. We hypothesized that c-kit plays a role in the survival, growth, and migration of CPCs. To test this hypothesis, human CPCs were grown under stress conditions in the presence or absence of SCF, and the effects of SCF-mediated activation of c-kit on CPC survival/growth and migration were measured. SCF treatment led to a significant increase in cell survival and a reduction in cell death under serum depletion conditions. In addition, SCF significantly promoted CPC migration in vitro. Furthermore, the pro-survival and pro-migratory effects of SCF were augmented by c-kit overexpression and abrogated by c-kit inhibition with imatinib. Mechanistically, c-kit activation in CPCs led to activation of the PI3K and the MAPK pathways. With the use of specific inhibitors, we confirmed that the SCF/c-kit-dependent survival and chemotaxis of CPCs are dependent on both pathways. Taken together, our findings suggest that c-kit promotes the survival/growth and migration of human CPCs cultured ex vivo via the activation of PI3K and MAPK pathways. These results imply that the efficiency of CPC homing to the injury site as well as their survival after transplantation may be improved by modulating the activity of c-kit.

Indexed as

ChemotaxisMAP Kinase Signaling SystemApoptosisCell ProliferationCell SurvivalEnzyme ActivationExtracellular Signal-Regulated MAP KinasesHumansMitogen-Activated Protein Kinase KinasesMyocardiumOxidative StressPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-kitStem Cell FactorStem CellsExtracellular Signal-Regulated MAP KinasesMitogen-Activated Protein Kinase KinasesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-kitStem Cell Factor

Identifiers

PMID26474484
PMCPMC4608800
OpenAlexW2266910759

What OpenQuestion holds

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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.