Inhibition of Let-7 microRNA attenuates myocardial remodeling and improves cardiac function postinfarction in mice
Autor: | Risto Kerkelä, Walter J. Koch, Johanna Magga, Raisa Serpi, Zoltan Szabo, Anne-Mari Moilanen, Pirkko Viitala, Ehre Gao, Anna-Maria Tolonen, Laura Vainio, Heikki Ruskoaho, Pauli Ohukainen |
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Rok vydání: | 2014 |
Předmět: |
Cardiac function curve
Cardiac output Pathology medicine.medical_specialty Cellular differentiation heart failure Apoptosis 030204 cardiovascular system & hematology fibroblast 03 medical and health sciences 0302 clinical medicine Medicine Myocardial infarction General Pharmacology Toxicology and Pharmaceutics Induced pluripotent stem cell 030304 developmental biology remodeling 0303 health sciences Ejection fraction microRNA business.industry Original Articles Let-7c medicine.disease 3. Good health Neurology Heart failure Cancer research Stem cell business |
Zdroj: | Pharmacology Research & Perspectives |
ISSN: | 2052-1707 |
Popis: | The members of lethal-7 (Let-7) microRNA (miRNA) family are involved in regulation of cell differentiation and reprogramming of somatic cells into induced pluripotent stem cells. However, their function in the heart is not known. In this study, we examined the effect of inhibiting the function of Let-7c miRNA on the progression of postinfarction left ventricular (LV) remodeling in mice. Myocardial infarction was induced with permanent ligation of left anterior descending coronary artery with a 4-week follow-up period. Let-7c miRNA was inhibited with a specific antagomir administered intravenously. The inhibition of Let-7c miRNA downregulated the levels of mature Let-7c miRNA and its other closely related members of Let-7 family in the heart and resulted in increased expression of pluripotency-associated genes Oct4 and Sox2 in cardiac fibroblasts in vitro and in adult mouse heart in vivo. Importantly, Let-7c inhibitor prevented the deterioration of cardiac function postinfarction, as demonstrated by preserved LV ejection fraction and elevated cardiac output. Improvement in cardiac function by Let-7c inhibitor postinfarction was associated with decreased apoptosis, reduced fibrosis, and reduction in the number of discoidin domain receptor 2-positive fibroblasts, while the number of c-kit(+) cardiac stem cells and Ki-67(+) proliferating cells remained unaltered. In conclusion, inhibition of Let-7 miRNA may be beneficial for the prevention of postinfarction LV remodeling and progression of heart failure. |
Databáze: | OpenAIRE |
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