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cardiomyocytes

Interindividual Heterogeneity Affects the Outcome of Human Cardiac Tissue Decellularization

[Scientific Reports] Scientists tested four methods to decellularize human cardiac tissue and evaluated their efficiency in terms of cell removal and preservation of key ECM components, such as collagens and sulfated glycosaminoglycans.

Development of Injectable Graphene Oxide/Laponite/Gelatin Hydrogel Containing Wharton’s Jelly Mesenchymal Stem Cells for Treatment of Oxidative Stress-Damaged Cardiomyocytes

[Colloids and Surfaces B-Biointerfaces] Injectable GO/laponite/gelatin (GO-LG) hydrogel was developed and characterized. The results of cell viability showed that the optimal concentration of GO flasks to treat cells was 100 μg/ml.

Repression of Osmr and Fgfr1 by miR-1/133a Prevents Cardiomyocyte Dedifferentiation and Cell Cycle Entry in the Adult Heart

[Science Advances] Scientists demonstrated that suppression of FGFR1 and OSMR by miR-1/133a was instrumental to prevent cardiomyocyte dedifferentiation and cell cycle entry in the adult heart.

METTL3 Improves Cardiomyocyte Proliferation upon Myocardial Infarction via Upregulating miR-17-3p in a DGCR8-Dependent Manner

[Cell Death Discovery] Due to the role of methyltransferase-like 3 (METTL3) in the physiological proliferation of cardiomyocytes, researchers aimed to determine whether METTL3 could also promote cardiomyocyte proliferation under pathological conditions and to elucidate the underlying mechanism.

A CRISPR/Cas9 Strategy for the Generation of a FLNC Knockout hESC Line (WAe009-a-70) to Model Dilated Cardiomyopathy and Arrhythmogenic Right Ventricular Cardiomyopathy

[Stem Cell Research] To further understand the exact role of FLNC in dilated cardiomyopathy, scientists generated a human FLNC knockout cell line from the original ESC line H9 by CRISPR/Cas9 gene editing technology.

Cell Proliferation Fate Mapping Reveals Regional Cardiomyocyte Cell-Cycle Activity in Subendocardial Muscle of Left Ventricle

[Nature Communications] Scientists found that the majority of cycling cardiomyocytes were positioned in the subendocardial muscle of the left ventricle, especially in the papillary muscles

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