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Title:
Accumulation of fibronectin in the heart after myocardial infarction: a putative stimulator of adhesion and proliferation of adipose-derived stem cells | Cell and Tissue Research
Description:
Stem cell therapy is a promising treatment after myocardial infarction (MI). A major problem in stem cell therapy, however, is that only a small proportion of stem cells applied to the heart can survive and differentiate into cardiomyocytes. We hypothesized that fibronectin in the heart after MI might positively affect stem cell adhesion and proliferation at the site of injury. Therefore, we investigated the kinetics of attachment and proliferation of adipose-tissue-derived stem cells (ASC) on fibronectin and analysed the time frame and localization of fibronectin accumulation in the human heart after MI. ASCs were seeded onto fibronectin-coated and uncoated culture wells. The numbers of adhering ASC were quantified after various incubation periods (5–30 min) by using DNA quantification assays. The proliferation of ASC was quantified after culturing ASC for various periods (0–9 days) by using DNA assays. Fibronectin accumulation after MI was quantified by immunohistochemical staining of heart sections from 35 patients, after different infarction periods (0–14 days old). We found that ASC attachment and proliferation on fibronectin-coated culture wells was significantly higher than on uncoated wells. Fibronectin deposition was significantly increased from 12 h to 14 days post-infarction, both in the infarction area and in the border-zone, compared with the uninfarcted heart. Our results suggest that a positive effect of fibronectin on stem cells in the heart can only be achieved when stem cell therapy is applied at least 12 h after MI, when the accumulation of fibronectin occurs in the infarcted heart.
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Keywords {🔍}
fibronectin, cells, infarction, stem, cell, heart, article, asc, attachment, myocardial, google, scholar, pubmed, area, culture, cas, phase, min, proliferation, cardiomyocytes, uncoated, wells, human, increased, compared, ami, tissue, cardiac, ecm, sections, fibronectincoated, deposition, depositions, therapy, infarct, significantly, positive, fig, found, infarcted, μgcm, van, ascs, days, pbs, accumulation, time, applied, staining, borderzone,
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biotin-conjugated swine-anti-rabbit antibodies streptavidin-biotin complex/horseradish peroxidase adipose-tissue-derived stem cells human bone-marrow-derived msc bone-marrow-derived stem cells anti-cd90 phycoerythrin-labelled antibody adipose-derived stem cells marrow-derived mesenchymal precursors exosomal mir-15a-5p article download pdf hypoxia-inducible factor 1alpha fluorescence-activated cell sorting paraffin-wax-embedded sections stained sterile phosphate-buffered saline short-term heart retention van der loo angiotensin-converting enzyme inhibitors human bone marrow mesenchymal stem cells stem cell retention stem cell transplantation full size image tissue research aims cardiac muscle cells privacy choices/manage cookies stem cell adhesion stem cell therapy van ham sm promotes osteogenic differentiation umbilical cord blood fibronectin-coated culture wells fibronectin-coated culture plates vu medical centre angiotensin-converting enzyme normal swine serum fibronectin-coated culture dishes myocardial tissue specimens rebuilding myocardial tissue sufficient stem cells adipose tissue ecm-coated culture plates stromal vascular fraction oedayrajsingh-varma anti-rabbit igg anti-death strategies single cell suspension graft cell death stem cell attachment tissue-harvesting procedure fibronectin promotes survival
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headline:Accumulation of fibronectin in the heart after myocardial infarction: a putative stimulator of adhesion and proliferation of adipose-derived stem cells
description:Stem cell therapy is a promising treatment after myocardial infarction (MI). A major problem in stem cell therapy, however, is that only a small proportion of stem cells applied to the heart can survive and differentiate into cardiomyocytes. We hypothesized that fibronectin in the heart after MI might positively affect stem cell adhesion and proliferation at the site of injury. Therefore, we investigated the kinetics of attachment and proliferation of adipose-tissue-derived stem cells (ASC) on fibronectin and analysed the time frame and localization of fibronectin accumulation in the human heart after MI. ASCs were seeded onto fibronectin-coated and uncoated culture wells. The numbers of adhering ASC were quantified after various incubation periods (5–30 min) by using DNA quantification assays. The proliferation of ASC was quantified after culturing ASC for various periods (0–9 days) by using DNA assays. Fibronectin accumulation after MI was quantified by immunohistochemical staining of heart sections from 35 patients, after different infarction periods (0–14 days old). We found that ASC attachment and proliferation on fibronectin-coated culture wells was significantly higher than on uncoated wells. Fibronectin deposition was significantly increased from 12 h to 14 days post-infarction, both in the infarction area and in the border-zone, compared with the uninfarcted heart. Our results suggest that a positive effect of fibronectin on stem cells in the heart can only be achieved when stem cell therapy is applied at least 12 h after MI, when the accumulation of fibronectin occurs in the infarcted heart.
datePublished:2008-02-28T00:00:00Z
dateModified:2008-02-28T00:00:00Z
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Stem cell
Heart
Adhesion
Infarction
Adipose tissue
Human
Human Genetics
Proteomics
Molecular Medicine
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headline:Accumulation of fibronectin in the heart after myocardial infarction: a putative stimulator of adhesion and proliferation of adipose-derived stem cells
description:Stem cell therapy is a promising treatment after myocardial infarction (MI). A major problem in stem cell therapy, however, is that only a small proportion of stem cells applied to the heart can survive and differentiate into cardiomyocytes. We hypothesized that fibronectin in the heart after MI might positively affect stem cell adhesion and proliferation at the site of injury. Therefore, we investigated the kinetics of attachment and proliferation of adipose-tissue-derived stem cells (ASC) on fibronectin and analysed the time frame and localization of fibronectin accumulation in the human heart after MI. ASCs were seeded onto fibronectin-coated and uncoated culture wells. The numbers of adhering ASC were quantified after various incubation periods (5–30 min) by using DNA quantification assays. The proliferation of ASC was quantified after culturing ASC for various periods (0–9 days) by using DNA assays. Fibronectin accumulation after MI was quantified by immunohistochemical staining of heart sections from 35 patients, after different infarction periods (0–14 days old). We found that ASC attachment and proliferation on fibronectin-coated culture wells was significantly higher than on uncoated wells. Fibronectin deposition was significantly increased from 12 h to 14 days post-infarction, both in the infarction area and in the border-zone, compared with the uninfarcted heart. Our results suggest that a positive effect of fibronectin on stem cells in the heart can only be achieved when stem cell therapy is applied at least 12 h after MI, when the accumulation of fibronectin occurs in the infarcted heart.
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Stem cell
Heart
Adhesion
Infarction
Adipose tissue
Human
Human Genetics
Proteomics
Molecular Medicine
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