Evidence map›Paper›PMID 21345805›Full record

ArticleCardiovascular research2011

VEGF/SDF-1 promotes cardiac stem cell mobilization and myocardial repair in the infarcted heart.

Jun-Ming Tang, Jia-Ning Wang, Lei Zhang, Fei Zheng, Jian-Ye Yang, Xia Kong, Lin-Yun Guo, Long Chen, Yong-Zhang Huang, Yu Wan and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cardiovascular research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 1 pooled it
11.4field-weighted citation impact, top 1% 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

140 citing papers in PubMed, 1 synthesis or guideline pooled it, 251 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
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  11. Endothelial Progenitor Cells: Disease Markers and Potential Therapy in Kidney Disease.Journal of the American Society of Nephrology : JASN · 2025
    Review
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  15. Article
  16. Therapeutic potential of CD73Histology and histopathology · 2025
    Review
  17. Review
  18. Review
  19. Review
  20. Article

80 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Jun-Ming TangInstitute of Clinical Medicine Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, PR China. tangjm416@163.com
Jia-Ning Wang
Lei Zhang
Fei Zheng
Jian-Ye Yang
Xia Kong
Lin-Yun Guo
Long Chen
Yong-Zhang Huang
Yu Wan
Shi-You Chen
Hubei University of Medicine · CNUniversity of Georgia · USWuhan University · CN

Funding

Smad2 and Smooth Muscle Differentiation from Neural Crest Stem CellsR01HL093429 · NHLBI · UNIVERSITY OF GEORGIA · PI CHEN, SHIYOU · 2008 to 2013
$2.0M
NHLBI NIH HHS HL093429NHLBI NIH HHS R01 HL093429
6 · The paper itself

Abstract

aimsThe objective of this study was to investigate whether vascular endothelial growth factor (VEGF) secreted by mesenchymal stem cells (MSC) improves myocardial survival and the engraftment of implanted MSC in infarcted hearts and promotes recruitment of stem cells through paracrine release of myocardial stromal cell-derived factor-1α (SDF-1α). METHODS AND

resultsVEGF-expressing MSC ((VEGF)MSC)-conditioned medium enhanced SDF-1α expression in heart slices and H9C2 cardiomyoblast cells via VEGF and the vascular endothelial growth factor receptor (VEGFR). The (VEGF)MSC-conditioned medium markedly promoted cardiac stem cell (CSC) migration at least in part via the SDF-1α/CXCR4 pathway and involved binding to VEGFR-1 and VEGFR-3. In vivo, (VEGF)MSC-stimulated SDF-1α expression in infarcted hearts resulted in massive mobilization and homing of bone marrow stem cells and CSC. Moreover, VEGF-induced SDF-1α guided the exogenously introduced CSC in the atrioventricular groove to migrate to the infarcted area, leading to a reduction in infarct size. Functional studies showed that (VEGF)MSC transplantation stimulated extensive angiomyogenesis in infarcted hearts as indicated by the expression of cardiac troponin T, CD31, and von Willebrand factor and improved the left ventricular performance, whereas blockade of SDF-1α or its receptor by RNAi or antagonist significantly diminished the beneficial effects of (VEGF)MSC.

conclusionExogenously expressed VEGF promotes myocardial repair at least in part through SDF-1α/CXCR4-mediated recruitment of CSC.

Indexed as

Cell MovementMesenchymal Stem Cell TransplantationRegenerationAnimalsCells, CulturedChemokine CXCL12Culture Media, ConditionedDisease Models, AnimalHumansMesenchymal Stem CellsMuscle DevelopmentMyocardial InfarctionMyocytes, CardiacNeovascularization, PhysiologicParacrine CommunicationPlatelet Endothelial Cell Adhesion Molecule-1Chemokine CXCL12Culture Media, ConditionedCxcr4 protein, ratPlatelet Endothelial Cell Adhesion Molecule-1Receptors, CXCR4Troponin TVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth Factor Receptor-3VEGFA protein, humanvon Willebrand Factor

Identifiers

PMID21345805
PMCPMC3139446
OpenAlexW2073319647

What OpenQuestion holds

Textmetadata
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.