Evidence map›Paper›PMID 18431364›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2008

Adult bone marrow-derived cells do not acquire functional attributes of cardiomyocytes when transplanted into peri-infarct myocardium.

John A Scherschel, Mark H Soonpaa, Edward F Srour, Loren J Field, Michael Rubart

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Frontiers in physiology · 2018
    Article
  3. Article
  4. Article
  5. Article
  6. c-kit(+) cells: the tell-tale heart of cardiac regeneration?Cellular and molecular life sciences : CMLS · 2015
    Review
  7. Article
  8. Intramyocardial cell delivery: observations in murine hearts.Journal of visualized experiments : JoVE · 2014
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Challenges for heart disease stem cell therapy.Vascular health and risk management · 2012
    Review
  14. Article
  15. CD117-positive cells of the heart: progenitor cells or mast cells?The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2010
    Article
  16. Article
  17. Interrogating functional integration between injected pluripotent stem cell-derived cells and surrogate cardiac tissue.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

John A ScherschelDepartment of Pediatrics, Division of Cardiology, Wells Center for Pediatric Research, Indianapolis, Indiana 46202, USA.
Mark H Soonpaa
Edward F Srour
Loren J Field
Michael Rubart
Indiana University – Purdue University Indianapolis · USCenter for Children · US

Funding

Genetic Enhancement of Cardiac Repair with Adult Stem CellsR01HL083126 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIELD, LOREN J · 2006 to 2015
$2.9M
Functional assessment of donor-host cell couplingR01HL075165 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI RUBART-VAN DER LOHE, MICHAEL · 2005 to 2009
$2.1M
NHLBI NIH HHS R01 HL075165NHLBI NIH HHS R01 HL083126
6 · The paper itself

Abstract

The cardiomyogenic potential of adult bone marrow (BM) cells after being directly transplanted into the ischemically injured heart remains a controversial issue. In this study, we investigated the ability of transplanted BM cells to develop intracellular calcium ([Ca(2+)](i)) transients in response to membrane depolarization in situ. Low-density mononuclear (LDM) BM cells, c-kit-enriched (c-kit(enr)) BM cells, and highly enriched lin(-) c-kit(+) BM cells were obtained from adult transgenic mice ubiquitously expressing enhanced green fluorescent protein (EGFP), and injected into peri-infarct myocardiums of nontransgenic mice. After 9-10 days the mice were killed, and the hearts were removed, perfused in Langendorff mode, loaded with the calcium-sensitive fluorophore rhod-2, and subjected to two-photon laser scanning fluorescence microscopy (TPLSM) to monitor action potential-induced [Ca(2+)](i) transients in EGFP-expressing donor-derived cells and non-expressing host cardiomyocytes. Whereas spontaneous and electrically evoked [Ca(2+)](i) transients were found to occur synchronously in host cardiomyocytes along the graft-host border and in areas remote from the infarct, they were absent in all of the >3,000 imaged BM-derived cells that were located in clusters throughout the infarct scar or peri-infarct zone. We conclude that engrafted BM-derived cells lack attributes of functioning cardiomyocytes, calling into question the concept that adult BM cells can give rise to substantive cardiomyocyte regeneration within the infarcted heart.

Indexed as

AnimalsAntigens, CD34Bone Marrow CellsCalciumCell LineageCell TransplantationChickensGreen Fluorescent ProteinsMiceMice, Inbred C57BLMicroscopy, FluorescenceModels, BiologicalMyocardial InfarctionMyocardiumMyocytes, CardiacAntigens, CD34CalciumGreen Fluorescent Proteins

Identifiers

PMID18431364
PMCPMC2574931
OpenAlexW2087935545

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.