Fibrosis and expression of extracellular matrix proteins in human interventricular septum in aortic valve stenosis and regurgitation
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
Cooperatio 207029
Charles University
RVO: 67985823
Czech Academy of Sciences
LX22NPO5104
European Union
IG220201
Ministerstvo Zdravotnictví Ceské Republiky
PubMed
38347221
PubMed Central
PMC11045568
DOI
10.1007/s00418-024-02268-y
PII: 10.1007/s00418-024-02268-y
Knihovny.cz E-zdroje
- Klíčová slova
- Collagen, Fibronectin, Fibrosis, Pressure overload, Valvular heart disease,
- MeSH
- aortální insuficience metabolismus patologie chirurgie MeSH
- aortální stenóza * metabolismus patologie chirurgie MeSH
- extracelulární matrix - proteiny * metabolismus analýza MeSH
- fibróza * metabolismus patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mezikomorová přepážka patologie metabolismus MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- extracelulární matrix - proteiny * MeSH
Valvular heart disease leads to ventricular pressure and/or volume overload. Pressure overload leads to fibrosis, which might regress with its resolution, but the limits and details of this reverse remodeling are not known. To gain more insight into the extent and nature of cardiac fibrosis in valve disease, we analyzed needle biopsies taken from the interventricular septum of patients undergoing surgery for valve replacement focusing on the expression and distribution of major extracellular matrix protein involved in this process. Proteomic analysis performed using mass spectrometry revealed an excellent correlation between the expression of collagen type I and III, but there was little correlation with the immunohistochemical staining performed on sister sections, which included antibodies against collagen I, III, fibronectin, sarcomeric actin, and histochemistry for wheat germ agglutinin. Surprisingly, the immunofluorescence intensity did not correlate significantly with the gold standard for fibrosis quantification, which was performed using Picrosirius Red (PSR) staining, unless multiplexed on the same tissue section. There was also little correlation between the immunohistochemical markers and pressure gradient severity. It appears that at least in humans, the immunohistochemical pattern of fibrosis is not clearly correlated with standard Picrosirius Red staining on sister sections or quantitative proteomic data, possibly due to tissue heterogeneity at microscale, comorbidities, or other patient-specific factors. For precise correlation of different types of staining, multiplexing on the same section is the best approach.
Cardiovascular Center Aalst OLV Clinic 9300 Aalst Belgium
Department of Cardiac Surgery 3rd Faculty of Medicine Charles University Prague Czech Republic
Institute of Physiology The Czech Academy of Sciences Videnska 1024 142 00 Prague Czech Republic
Na Homolce Hospital Roentgenova 37 2 150 30 Prague Czech Republic
University Hospital Kralovske Vinohrady Prague Czech Republic
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