Evidence map›Paper›PMID 23083931›Full record

ArticleBiomaterials2013

The effect of controlled expression of VEGF by transduced myoblasts in a cardiac patch on vascularization in a mouse model of myocardial infarction.

Anna Marsano, Robert Maidhof, Jianwen Luo, Kana Fujikara, Elisa E Konofagou, Andrea Banfi, Gordana Vunjak-Novakovic

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Engineering Three-Dimensional Vascularized Cardiac Tissues.Tissue engineering. Part B, Reviews · 2022
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Therapeutic vascularization in regenerative medicine.Stem cells translational medicine · 2020
    Review
  12. Current advances in biodegradable synthetic polymer based cardiac patches.Journal of biomedical materials research. Part A · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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 2 countries.

Anna MarsanoColumbia University, Department of Biomedical Engineering, New York, NY 10032, USA.
Robert Maidhof
Jianwen Luo
Kana Fujikara
Elisa E Konofagou
Andrea Banfi
Gordana Vunjak-Novakovic
Columbia University · USUniversity Hospital of Basel · CH

Funding

Translational Bioreactors - Engineering Complex TissuesP41EB002520 · NIBIB · TUFTS UNIVERSITY MEDFORD · PI KAPLAN, DAVID L. · 2004 to 2018
$16.7M
Engineering Vascularized Cardiac MuscleR01HL076485 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Gordana Vunjak-Novakovic · 2005 to 2026
$9.2M
Enhancing survival and function of engineered cardiac tissueR21HL108668 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SANTAMBROGIO, LAURA, VUNJAK-NOVAKOVIC, GORDANA · 2011 to 2012
$461k
Controlled gene delivery for in vivo vascularization of an engineered cardiac patR21HL089913 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI VUNJAK-NOVAKOVIC, GORDANA · 2008 to 2009
$403k
NHLBI NIH HHS HL076485NHLBI NIH HHS HL088913NHLBI NIH HHS R01 HL076485NHLBI NIH HHS R21 HL089913NHLBI NIH HHS R21 HL108668NIBIB NIH HHS EB002520NIBIB NIH HHS P41 EB002520
6 · The paper itself

Abstract

Key requirements for cardiac tissue engineering include the maintenance of cell viability and function and the establishment of a perfusable vascular network in millimeters thick and compact cardiac constructs upon implantation. We investigated if these requirements can be met by providing an intrinsic vascularization stimulus (via sustained action of VEGF secreted at a controlled rate by transduced myoblasts) to a cardiac patch engineered under conditions of effective oxygen supply (via medium flow through channeled elastomeric scaffolds seeded with neonatal cardiomyocytes). We demonstrate that this combined approach resulted in increased viability, vascularization and functionality of the cardiac patch. After implantation in a mouse model of myocardial infarction, VEGF-expressing patches displayed significantly improved engraftment, survival and differentiation of cardiomyocytes, leading to greatly enhanced contractility as compared to controls not expressing VEGF. Controlled VEGF expression also mediated the formation of mature vascular networks, both within the engineered patches and in the underlying ischemic myocardium. We propose that this combined cell-biomaterial approach can be a promising strategy to engineer cardiac patches with intrinsic and extrinsic vascularization potential.

Indexed as

AnimalsCells, CulturedCell SurvivalCoculture TechniquesCoronary VesselsMiceMice, Inbred C57BLMyoblastsMyocardial InfarctionMyocardiumMyocytes, CardiacNeovascularization, PhysiologicRatsRats, Sprague-DawleyTissue EngineeringTissue ScaffoldsVascular Endothelial Growth Factor A

Identifiers

PMID23083931
PMCPMC3490044
OpenAlexW2091861445

What OpenQuestion holds

Textmetadata
LicenceTDM
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.