Evidence map›Paper›PMID 11390421›Full record

ArticleThe Journal of clinical investigation2001

Regeneration of ischemic cardiac muscle and vascular endothelium by adult stem cells.

K A Jackson, S M Majka, H Wang, J Pocius, C J Hartley, M W Majesky, M L Entman, L H Michael, K K Hirschi, M A Goodell

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 424 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
424citing papers in PubMed, 1 pooled it
62.7field-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.

NCT00765050 phase1 / phase2terminatednot on this mapstarted 2009, after this paper: background citation

A Prospective, Open, Non-randomized Phase I/II Study of Therapeutic Angiogenesis in Diabetic Patients With Critic Ischemia of Lower Limbs While Administering Positive CD133 Mobilized With G-CSF

TypeinterventionalSponsorPETHEMA FoundationRan2009 to 2012Enrolled13ConditionsDiabetic Patients With Critic Ischemia in Lower Limbs Who Are Administered With CD133+ Cells Mobilized by G-CSFArmsCD133+ cells transplant
NCT01049867 phase1 / phase2unknown statusnot on this mapstarted 2009, after this paper: background citation

Phase 1-2 Study of Intracoronary Infusion of CD133+ Endothelial Precursor Cells for Patients With Coronary Heart Disease in Selected Obstructed Artery

TypeinterventionalSponsorHospital y Clinica OCA, S.A. de C.V.Ran2009 to 2011Enrolled10ConditionsCoronary Artery DiseaseArmsIntracoronary Infusion of CD133+ Cells
3 · Its place in the literature

Who cites it

424 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,965 citations in OpenAlex.

  1. The effect of bone marrow mononuclear stem cell therapy on left ventricular function and myocardial perfusion.Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology · 2014
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364 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

K A JacksonCenter for Cell and Gene Therapy and Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
S M Majka
H Wang
J Pocius
C J Hartley
M W Majesky
M L Entman
L H Michael
K K Hirschi
M A Goodell
Baylor College of Medicine · USHouston Methodist · US

Funding

ROLE OF INFLAMMATION IN EARLY MYOCARDIAL ISCHEMIAP01HL042550 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI ENTMAN, MARK L · 1990 to 2004
$10.4M
RETINOID REGULATION OF BLOOD VESSEL FORMATIONR01HL061408 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI HIRSCHI, KAREN K · 2000 to 2004
$1.5M
SYMPATHETIC TROPHIC EFFECTS ON ARTERIAL SMOOTH MUSCLER01HL047655 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MAJESKY, MARK W. · 1992 to 1996
–
NHLBI NIH HHS HL-42550NHLBI NIH HHS HL-47655NHLBI NIH HHS P01 HL042550NHLBI NIH HHS R01 HL061408PHS HHS H-L61408
6 · The paper itself

Abstract

Myocyte loss in the ischemically injured mammalian heart often leads to irreversible deficits in cardiac function. To identify a source of stem cells capable of restoring damaged cardiac tissue, we transplanted highly enriched hematopoietic stem cells, the so-called side population (SP) cells, into lethally irradiated mice subsequently rendered ischemic by coronary artery occlusion for 60 minutes followed by reperfusion. The engrafted SP cells (CD34(-)/low, c-Kit(+), Sca-1(+)) or their progeny migrated into ischemic cardiac muscle and blood vessels, differentiated to cardiomyocytes and endothelial cells, and contributed to the formation of functional tissue. SP cells were purified from Rosa26 transgenic mice, which express lacZ widely. Donor-derived cardiomyocytes were found primarily in the peri-infarct region at a prevalence of around 0.02% and were identified by expression of lacZ and alpha-actinin, and lack of expression of CD45. Donor-derived endothelial cells were identified by expression of lacZ and Flt-1, an endothelial marker shown to be absent on SP cells. Endothelial engraftment was found at a prevalence of around 3.3%, primarily in small vessels adjacent to the infarct. Our results demonstrate the cardiomyogenic potential of hematopoietic stem cells and suggest a therapeutic strategy that eventually could benefit patients with myocardial infarction.

Indexed as

Hematopoietic Stem Cell TransplantationAnimalsbeta-GalactosidaseBone MarrowEndothelium, VascularHematopoietic Stem CellsHumansImmunohistochemistryMiceMice, Inbred C57BLMice, TransgenicMyocardial InfarctionMyocardial IschemiaMyocardiumRegenerationbeta-Galactosidase

Identifiers

PMID11390421
PMCPMC209322
OpenAlexW2104898886

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.