Studying the Fate of Tumor Extracellular Vesicles at High Spatiotemporal Resolution Using the Zebrafish Embryo.

Tumor extracellular vesicles (EVs) mediate the communication between tumor and stromal cells mostly to the benefit of tumor progression. Notably, tumor EVs travel in the bloodstream, reach distant organs, and locally modify the microenvironment. However, visualizing these events in vivo still faces...

ver descrição completa

Detalhes bibliográficos
Autores: Hyenne, Vincent, Ghoroghi, Shima, Collot, Mayeul, Bons, Joanna, Follain, Gautier, Harlepp, Sébastien, Mary, Benjamin, Bauer, Jack, Mercier, Luc, Busnelli, Ignacio, Lefebvre, Olivier, Fekonja, Nina, Garcia-Leon, Maria J, Machado, Pedro, Delalande, François, López, Ana Amor, Silva, Susana Garcia, Verweij, Frederik J, van Niel, Guillaume, Djouad, Farida, Peinado, Héctor, Carapito, Christine, Klymchenko, Andrey S, Goetz, Jacky G
Tipo de documento: artigo
Data de publicação:2019
País:España
Recursos:Instituto de Salud Carlos III (ISCIII)
Repositório:Repisalud
Idioma:inglês
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/27251
Acesso em linha:https://hdl.handle.net/20.500.12105/27251
Access Level:Acceso aberto
Palavra-chave:correlated light and electron microscopy
exosomes
extracellular vesicles
patrolling macrophages
premetastatic niche
zebrafish
Descrição
Resumo:Tumor extracellular vesicles (EVs) mediate the communication between tumor and stromal cells mostly to the benefit of tumor progression. Notably, tumor EVs travel in the bloodstream, reach distant organs, and locally modify the microenvironment. However, visualizing these events in vivo still faces major hurdles. Here, we describe an approach for tracking circulating tumor EVs in a living organism: we combine chemical and genetically encoded probes with the zebrafish embryo as an animal model. We provide a first description of tumor EVs' hemodynamic behavior and document their intravascular arrest. We show that circulating tumor EVs are rapidly taken up by endothelial cells and blood patrolling macrophages and subsequently stored in degradative compartments. Finally, we demonstrate that tumor EVs activate macrophages and promote metastatic outgrowth. Overall, our study proves the usefulness and prospects of zebrafish embryo to track tumor EVs and dissect their role in metastatic niches formation in vivo.