Artigo Acesso aberto Revisado por pares

Exosomes secreted by cardiomyocytes subjected to ischaemia promote cardiac angiogenesis

2017; Oxford University Press; Volume: 113; Issue: 11 Linguagem: Inglês

10.1093/cvr/cvx118

ISSN

1755-3245

Autores

Teresa Ribeiro‐Rodrigues, Tiago L. Laundos, Rita Carvalho, Daniela Batista-Almeida, Ricardo Pereira, Vanessa Coelho‐Santos, Ana Paula Silva, Rosa Fernandes, Mónica Zuzarte, Francisco J. Enguita, Marina C. Costa, Perpétua Pinto‐do‐Ó, Marta Pinto, Pedro Gouveia, Lino Ferreira, Justin C. Mason, Paulo Pereira, Brenda R. Kwak, Diana S. Nascimento, Henrique Girão,

Tópico(s)

Cardiovascular Effects of Exercise

Resumo

Myocardial infarction (MI) is the leading cause of morbidity and mortality worldwide and results from an obstruction in the blood supply to a region of the heart. In an attempt to replenish oxygen and nutrients to the deprived area, affected cells release signals to promote the development of new vessels and confer protection against MI. However, the mechanisms underlying the growth of new vessels in an ischaemic scenario remain poorly understood. Here, we show that cardiomyocytes subjected to ischaemia release exosomes that elicit an angiogenic response of endothelial cells (ECs).Exosomes secreted by H9c2 myocardial cells and primary cardiomyocytes, cultured either in control or ischaemic conditions were isolated and added to ECs. We show that ischaemic exosomes, in comparison with control exosomes, confer protection against oxidative-induced lesion, promote proliferation, and sprouting of ECs, stimulate the formation of capillary-like structures and strengthen adhesion complexes and barrier properties. Moreover, ischaemic exosomes display higher levels of metalloproteases (MMP) and promote the secretion of MMP by ECs. We demonstrate that miR-222 and miR-143, the relatively most abundant miRs in ischaemic exosomes, partially recapitulate the angiogenic effect of exosomes. Additionally, we show that ischaemic exosomes stimulate the formation of new functional vessels in vivo using in ovo and Matrigel plug assays. Finally, we demonstrate that intramyocardial delivery of ischaemic exosomes improves neovascularization following MI.This study establishes that exosomes secreted by cardiomyocytes under ischaemic conditions promote heart angiogenesis, which may pave the way towards the development of add-on therapies to enhance myocardial blood supply.

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