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cardiac fibroblasts

AAV-Mediated YAP Expression in Cardiac Fibroblasts Promotes Inflammation and Increases Fibrosis

[Scientific Reports] Researchers leveraged adeno-associated virus (AAV) to target cardiac fibroblasts and demonstrated that chronic Yes-associated protein (YAP) expression upregulated indices of fibrosis and inflammation in the absence of additional stress.

A Predictive In Vitro Risk Assessment Platform for Pro-Arrhythmic Toxicity Using Human 3D Cardiac Microtissues

[Scientific Reports] Scientists used human induced pluripotent stem cell-derived cardiomyocytes and human cardiac fibroblasts in 3-dimensional microtissues to create an improved in vitro platform for assessing pro-arrhythmic cardiotoxicity.

Multiplexed Targeting of miRNA-210 in Stem Cell-Derived Extracellular Vesicles Promotes Selective Regeneration in Ischemic Hearts

[Experimental and Molecular Medicine] Under hypoxic conditions, the authors observed that ASCmiR-210 inhibited apoptosis by modulating protein tyrosine phosphatase 1B and death-associated protein kinase 1.

Prevention of Fibrosis and Pathological Cardiac Remodeling by Salinomycin

[Circulation Research] Scientists demonstrated that salinomycin displayed potent anti-fibrotic activity in cardiac fibroblasts obtained from heart failure patients. In pre-clinical studies, salinomycin prevented cardiac fibrosis and functional decline in mouse models of ischemic and non-ischemic heart disease.

Generation, Functional Analysis and Applications of Isogenic Three-Dimensional Self-Aggregating Cardiac Microtissues from Human Pluripotent Stem Cells

[Nature Protocols] Scientists describe a protocol to generate cardiomyocytes, cardiac fibroblasts and cardiac endothelial cells, the three principal cell types in the heart, from human induced pluripotent stem cells and combine them in 3D cardiac microtissues.

Small Extracellular Vesicles Containing miR-486-5p Promote Angiogenesis after Myocardial Infarction in Mice and Nonhuman Primates

[Science Translational Medicine] Investigators observed improved cardiac function, enhanced vascular density, and smaller infarct size in mice treated with the small extracellular vesicles from hypoxia-preconditioned mesenchymal stem cells (MSCs) than in mice treated with normoxia-preconditioned MSCs.

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