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Expression of Osteopontin and Gremlin 1 Proteins in Cardiomyocytes in Ischemic Heart Failure
Milda Kuprytė1, Vaiva Lesauskaitė2, Vitalija Siratavičiūtė1
1Laboratory of Cardiac Pathology, Institute of Cardiology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.
Insights
Osteopontin (OPN) and gremlin 1 (Grem1) show increased expression in cardiomyocytes during early stages of ischemic heart failure (HF). These proteins significantly contribute to cellular remodeling and the progression of HF.
Area of Science:
- Cardiovascular Biology
- Molecular Cardiology
- Heart Failure Pathogenesis
Background:
- Osteopontin (OPN) and gremlin 1 (Grem1) are implicated in cardiac remodeling and heart failure (HF).
- Previous studies focused on plasma levels and advanced HF stages.
- Early protein expression changes in cardiomyocytes during chronic ischemic HF remain understudied.
Purpose of the Study:
- To investigate OPN and Grem1 protein expression changes in human cardiomyocytes across different stages of ischemic HF.
- To elucidate the role of OPN and Grem1 in early cardiomyocyte remodeling.
Main Methods:
- Semi-quantitative immunohistochemical analysis of 105 human left ventricular myocardial tissue samples.
- Assessment of OPN and Grem1 protein expression intensity.
- Correlation analysis with cardiomyocyte diameter and length.
Main Results:
- Increased OPN and Grem1 immunostaining intensity observed from Stage A HF, progressively rising through Stages B and C/D.
- Significant positive correlations found between OPN/Grem1 expression and cardiomyocyte diameter/length.
- A positive correlation was noted between OPN and Grem1 expression levels within cardiomyocytes.
Conclusions:
- OPN and Grem1 are significantly upregulated in cardiomyocytes during early ischemic HF.
- These proteins play a crucial role in the initial stages of cardiomyocyte remodeling and geometric reorganization.
- Findings offer new insights into the pathogenesis of ischemic heart failure.
Abstract:
A relevant role of osteopontin (OPN) and gremlin 1 (Grem1) in regulating cardiac tissue remodeling and formation of heart failure (HF) are documented, with the changes of OPN and Grem1 levels in blood plasma due to acute ischemia, ischemic heart disease-induced advanced HF or dilatative cardiomyopathy being the primary focus in most of these studies. However, knowledge on the early OPN and Grem1 proteins expression changes within cardiomyocytes during remodeling due to chronic ischemia remains insufficient. The aim of this study was to determine the OPN and Grem1 proteins expression changes in human cardiomyocytes at different stages of ischemic HF. A semi-quantitative immunohistochemical analysis was performed in 105 myocardial tissue samples obtained from the left cardiac ventricles. Increased OPN immunostaining intensity was already detected in the stage A HF group, compared to the control group (p < 0.001), and continued to increase in the stage B HF (p < 0.001), achieving the peak of immunostaining in the stages C/D HF group (p < 0.001). Similar data of Grem1 immunostaining intensity changes in cardiomyocytes were documented. Significantly positive correlations were detected between OPN, Grem1 expression in cardiomyocytes and their diameter as well as the length, in addition to positive correlation between OPN and Grem1 expression changes within cardiomyocytes. These novel findings suggest that OPN and Grem1 contribute significantly to reorganization of cellular geometry from the earliest stage of cardiomyocyte remodeling, providing new insights into the ischemic HF pathogenesis.
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