| Literature DB >> 30745140 |
Vincent Hyenne1, Shima Ghoroghi2, Mayeul Collot3, Joanna Bons4, Gautier Follain2, Sébastien Harlepp2, Benjamin Mary2, Jack Bauer2, Luc Mercier2, Ignacio Busnelli2, Olivier Lefebvre2, Nina Fekonja2, Maria J Garcia-Leon2, Pedro Machado5, François Delalande4, Ana Amor López6, Susana Garcia Silva6, Frederik J Verweij7, Guillaume van Niel7, Farida Djouad8, Héctor Peinado6, Christine Carapito4, Andrey S Klymchenko3, Jacky G Goetz9.
Abstract
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.Entities:
Keywords: correlated light and electron microscopy; exosomes; extracellular vesicles; patrolling macrophages; premetastatic niche; zebrafish
Mesh:
Year: 2019 PMID: 30745140 DOI: 10.1016/j.devcel.2019.01.014
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270