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C-kit(pos) cells in the human left atrial appendage
BACKGROUND: Subpopulations of myocardial c-kit(pos) cells have the ability to stimulate regeneration in ischemic heart disease by paracrine effects. The left atrial appendage (LAA), which is easy accessible during cardiac surgery, may represent a perfect source for c-kit(pos) cell extraction for aut...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637945/ https://www.ncbi.nlm.nih.gov/pubmed/37954289 http://dx.doi.org/10.1016/j.heliyon.2023.e21268 |
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author | Schwarzkopf, Lea Büttner, Petra Scholtyssek, Karl Schröter, Thomas Hiller, Ruth Hindricks, Gerhard Bollmann, Andreas Laufs, Ulrich Ueberham, Laura |
author_facet | Schwarzkopf, Lea Büttner, Petra Scholtyssek, Karl Schröter, Thomas Hiller, Ruth Hindricks, Gerhard Bollmann, Andreas Laufs, Ulrich Ueberham, Laura |
author_sort | Schwarzkopf, Lea |
collection | PubMed |
description | BACKGROUND: Subpopulations of myocardial c-kit(pos) cells have the ability to stimulate regeneration in ischemic heart disease by paracrine effects. The left atrial appendage (LAA), which is easy accessible during cardiac surgery, may represent a perfect source for c-kit(pos) cell extraction for autologous cell therapies in the living human. So far, frequency and distribution of c-kit(pos) cells in LAA are unknown. METHODS: LAAs of patients who underwent cardiac surgery due to coronary artery disease (coronary artery bypass graft, CABG), valvular heart disease or both and of two body donors were examined. Tissue was fixed in 4 % paraformaldehyde, embedded in paraffin, dissected in consecutive sections and stained for c-kit(pos) cells. In parallel, grade of fibrosis, amount of fat per section and cells positive for mast cell tryptase were examined. RESULTS: We collected 27 LAAs (37.0 % female, mean left ventricular ejection fraction 50.4 %, 63.0 % persistent atrial fibrillation (AF)). Most of the patients underwent combined CABG and valve surgery (51.9 %). C-kit(pos) cells were detected in 3 different regions: A) Attached to the epicardial fat layer, B) close to vascular structures and C) between cardiomyocytes. C-kit(pos) cells ranged from 0.05 c-kit(pos) cells per mm(2) to 67.5 c-kit(pos) cells per mm(2). We found no association between number of c-kit(pos) cells and type of AF, amount of fibrosis or amount of fat. Up to 72 % of c-kit(pos) cells also showed a positive staining for mast cell tryptase. CONCLUSION: C-kit(pos) cells are frequent in LAAs of cardiovascular patients with a rather homogenous distribution throughout the LAA. The LAA can therefore be considered as a source for extraction of a reasonable quantity of autologous cardiac progenitor cells in the living human patient. |
format | Online Article Text |
id | pubmed-10637945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-106379452023-11-11 C-kit(pos) cells in the human left atrial appendage Schwarzkopf, Lea Büttner, Petra Scholtyssek, Karl Schröter, Thomas Hiller, Ruth Hindricks, Gerhard Bollmann, Andreas Laufs, Ulrich Ueberham, Laura Heliyon Research Article BACKGROUND: Subpopulations of myocardial c-kit(pos) cells have the ability to stimulate regeneration in ischemic heart disease by paracrine effects. The left atrial appendage (LAA), which is easy accessible during cardiac surgery, may represent a perfect source for c-kit(pos) cell extraction for autologous cell therapies in the living human. So far, frequency and distribution of c-kit(pos) cells in LAA are unknown. METHODS: LAAs of patients who underwent cardiac surgery due to coronary artery disease (coronary artery bypass graft, CABG), valvular heart disease or both and of two body donors were examined. Tissue was fixed in 4 % paraformaldehyde, embedded in paraffin, dissected in consecutive sections and stained for c-kit(pos) cells. In parallel, grade of fibrosis, amount of fat per section and cells positive for mast cell tryptase were examined. RESULTS: We collected 27 LAAs (37.0 % female, mean left ventricular ejection fraction 50.4 %, 63.0 % persistent atrial fibrillation (AF)). Most of the patients underwent combined CABG and valve surgery (51.9 %). C-kit(pos) cells were detected in 3 different regions: A) Attached to the epicardial fat layer, B) close to vascular structures and C) between cardiomyocytes. C-kit(pos) cells ranged from 0.05 c-kit(pos) cells per mm(2) to 67.5 c-kit(pos) cells per mm(2). We found no association between number of c-kit(pos) cells and type of AF, amount of fibrosis or amount of fat. Up to 72 % of c-kit(pos) cells also showed a positive staining for mast cell tryptase. CONCLUSION: C-kit(pos) cells are frequent in LAAs of cardiovascular patients with a rather homogenous distribution throughout the LAA. The LAA can therefore be considered as a source for extraction of a reasonable quantity of autologous cardiac progenitor cells in the living human patient. Elsevier 2023-10-26 /pmc/articles/PMC10637945/ /pubmed/37954289 http://dx.doi.org/10.1016/j.heliyon.2023.e21268 Text en © 2023 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Schwarzkopf, Lea Büttner, Petra Scholtyssek, Karl Schröter, Thomas Hiller, Ruth Hindricks, Gerhard Bollmann, Andreas Laufs, Ulrich Ueberham, Laura C-kit(pos) cells in the human left atrial appendage |
title | C-kit(pos) cells in the human left atrial appendage |
title_full | C-kit(pos) cells in the human left atrial appendage |
title_fullStr | C-kit(pos) cells in the human left atrial appendage |
title_full_unstemmed | C-kit(pos) cells in the human left atrial appendage |
title_short | C-kit(pos) cells in the human left atrial appendage |
title_sort | c-kit(pos) cells in the human left atrial appendage |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637945/ https://www.ncbi.nlm.nih.gov/pubmed/37954289 http://dx.doi.org/10.1016/j.heliyon.2023.e21268 |
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