miR-146a targets Fos expression in human cardiac cells

miR-146a is a microRNA whose transcript levels are induced in the heart upon activation of NF-kappa B, a transcription factor induced by proinflammatory molecules (such as TNF-alpha) that is strongly related to the pathogenesis of cardiac disorders. The main goal of this study consisted of studying...

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Detalhes bibliográficos
Autores: Palomer, X, Capdevila-Busquets, E, Botteri, G, Davidson, MM, Rodriguez, C, Martinez-Gonzalez, J, Vidal, F, Barroso, E, Chan, TO, Feldman, AM, Vazquez-Carrera, M
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:España
Recursos:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
Repositorio:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
OAI Identifier:oai:iibsantpau.fundanetsuite.com:p8370
Acesso em linha:https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=8370
Access Level:acceso abierto
Palavra-chave:Fos
Cardiac remodeling
Inflammation
miR-146a
Matrix metalloproteinase-9
Descrição
Resumo:miR-146a is a microRNA whose transcript levels are induced in the heart upon activation of NF-kappa B, a transcription factor induced by proinflammatory molecules (such as TNF-alpha) that is strongly related to the pathogenesis of cardiac disorders. The main goal of this study consisted of studying new roles of miR-146a in cardiac pathological processes caused by the pro-inflammatory cytokine TNF-alpha. Our results demonstrate that miR-146a transcript levels were sharply increased in cardiac ventricular tissue of transgenic mice with specific overexpression of TNF-alpha in the heart, and also in a cardiomyocyte cell line of human origin (AC16) exposed to TNF-alpha. Among all the in silico predicted miR-146a target genes, Fos mRNA and protein levels notably decreased after TNF-alpha treatment or miR-146a overexpression. These changes correlated with a diminution in the DNA-binding activity of AP-1, the Fos-containing transcription factor complex. Interestingly, AP-1 inhibition was accompanied by a reduction in matrix metalloproteinase (MMP)-9 mRNA levels in human cardiac cells. The specific regulation of this MMP by miR-146a was further confirmed at the secretion and enzymatic activity levels, as well as after anti-miR-mediated miR-146a inhibition. The results reported here demonstrate that Fos is a direct target of miR-146a activity and that downregulation of the Fos-AP-1 pathway by miR-146a has the capacity to inhibit MMP-9 activity. Given that MMP-9 is an AP-1 target gene involved in cardiac remodeling, myocardial dysfunction and progression of heart failure, these findings suggest that miR-146a might be a new and promising therapeutic tool for treating cardiac disorders associated with enhanced inflammation in the heart.