Evidence map›Paper›PMID 24722830›Full record

ArticleClinical research in cardiology : official journal of the German Cardiac Society2014

Characteristic of c-Kit+ progenitor cells in explanted human hearts.

Sybilla Matuszczak, Justyna Czapla, Magdalena Jarosz-Biej, Ewa Wiśniewska, Tomasz Cichoń, Ryszard Smolarczyk, Magdalena Kobusińska, Karolina Gajda, Piotr Wilczek, Joanna Sliwka and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical research in cardiology : official journal of the German Cardiac Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Sybilla MatuszczakCenter for Translational Research and Molecular Biology of Cancer, Maria Skłodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice Branch, Wybrzeże Armii Krajowej Street 15, 44-101, Gliwice, Poland.
Justyna Czapla
Magdalena Jarosz-Biej
Ewa Wiśniewska
Tomasz Cichoń
Ryszard Smolarczyk
Magdalena Kobusińska
Karolina Gajda
Piotr Wilczek
Joanna Sliwka
Michał Zembala
Marian Zembala
Stanisław Szala
The Maria Sklodowska-Curie National Research Institute of Oncology · PLSilesian Center for Heart Disease · PLFoundation of Cardiac Surgery Development · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

According to literature data, self-renewing, multipotent, and clonogenic cardiac c-Kit(+) progenitor cells occur within human myocardium. The aim of this study was to isolate and characterize c-Kit(+) progenitor cells from explanted human hearts. Experimental material was obtained from 19 adult and 7 pediatric patients. Successful isolation and culture was achieved for 95 samples (84.1%) derived from five different regions of the heart: right and left ventricles, atrium, intraventricular septum, and apex. The average percentage of c-Kit(+) cells, as assessed by FACS, ranged between 0.7 and 0.9%. In contrast to published data we do not observed statistically significant differences in the number of c-Kit(+) cells between disease-specific groups, parts of the heart or sexes. Nevertheless, c-Kit(+) cells were present in significant numbers (11-24%) in samples derived from three explanted pediatric hearts. c-Kit(+) cells were also positive for CD105 and a majority of them was positive for CD31 and CD34 (83.7 ± 8.6 and 75.7 ± 11.4%, respectively). Immunohistochemical analysis of the heart tissue revealed that most cells possessing the c-Kit antigen were also positive for tryptase, a specific mast cell marker. However, flow cytometry analysis has shown cultured c-Kit(+) cells to be negative for hematopoietic marker CD45 and mast cell marker CD33. Isolated c-Kit(+) cells display mesenchymal stem cell features and are thought to differentiate into endothelial cells.

Indexed as

AdolescentAdultAgedAge FactorsAntigens, CDBiomarkersCell DifferentiationChildChild, PreschoolFemaleFlow CytometryHumansHuman Umbilical Vein Endothelial CellsImmunohistochemistryMaleMesenchymal Stem CellsAntigens, CDBiomarkersProto-Oncogene Proteins c-kitTryptases

Identifiers

PMID24722830
PMCPMC4129222
OpenAlexW2061532186

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Registered trials

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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.