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We are analyzing https://link.springer.com/article/10.1007/s00441-008-0573-0.

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.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
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Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,642,828 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We can't figure out the monetization strategy.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

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,

Topics {✒️}

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

Schema {🗺️}

WebPage:
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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
         pageStart:289
         pageEnd:298
         license:https://creativecommons.org/licenses/by-nc/2.0
         sameAs:https://doi.org/10.1007/s00441-008-0573-0
         keywords:
            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.
      datePublished:2008-02-28T00:00:00Z
      dateModified:2008-02-28T00:00:00Z
      pageStart:289
      pageEnd:298
      license:https://creativecommons.org/licenses/by-nc/2.0
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      keywords:
         Stem cell
         Heart
         Adhesion
         Infarction
         Adipose tissue
         Human
         Human Genetics
         Proteomics
         Molecular Medicine
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            name:VU University Medical Centre
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            name:VU University Medical Centre
            address:
               name:ICaR-VU, Institute of Cardiovascular Research, VU University Medical Centre, Amsterdam, The Netherlands
               type:PostalAddress
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               type:PostalAddress
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               name:Department of Clinical Epidemiology and Biostatistics, VU University Medical Centre, Amsterdam, The Netherlands
               type:PostalAddress
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            name:VU University Medical Centre
            address:
               name:Department of Cardiology, VU University Medical Centre, Amsterdam, The Netherlands
               type:PostalAddress
            type:Organization
            name:VU University Medical Centre
            address:
               name:ICaR-VU, Institute of Cardiovascular Research, VU University Medical Centre, Amsterdam, The Netherlands
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            type:Organization
      name:F. J. van Milligen
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            address:
               name:Department of Pathology, ICaR-VU, VU University Medical Centre, Amsterdam, The Netherlands
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PostalAddress:
      name:Department of Pathology, ICaR-VU, VU University Medical Centre, Amsterdam, The Netherlands
      name:ICaR-VU, Institute of Cardiovascular Research, VU University Medical Centre, Amsterdam, The Netherlands
      name:Department of Pathology, ICaR-VU, VU University Medical Centre, Amsterdam, The Netherlands
      name:Department of Cardiac Surgery, VU University Medical Centre, Amsterdam, The Netherlands
      name:ICaR-VU, Institute of Cardiovascular Research, VU University Medical Centre, Amsterdam, The Netherlands
      name:Department of Pathology, ICaR-VU, VU University Medical Centre, Amsterdam, The Netherlands
      name:Department of Clinical Epidemiology and Biostatistics, VU University Medical Centre, Amsterdam, The Netherlands
      name:Department of Cardiology, VU University Medical Centre, Amsterdam, The Netherlands
      name:ICaR-VU, Institute of Cardiovascular Research, VU University Medical Centre, Amsterdam, The Netherlands
      name:Department of Pathology, ICaR-VU, VU University Medical Centre, Amsterdam, The Netherlands

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