Studying the Fate of Tumor Extracellular Vesicles at High Spatiotemporal Resolution Using the Zebrafish Embryo.
correlated light and electron microscopy
exosomes
extracellular vesicles
patrolling macrophages
premetastatic niche
zebrafish
Journal
Developmental cell
ISSN: 1878-1551
Titre abrégé: Dev Cell
Pays: United States
ID NLM: 101120028
Informations de publication
Date de publication:
25 02 2019
25 02 2019
Historique:
received:
15
03
2018
revised:
19
10
2018
accepted:
10
01
2019
pubmed:
13
2
2019
medline:
23
8
2019
entrez:
13
2
2019
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 30745140
pii: S1534-5807(19)30014-0
doi: 10.1016/j.devcel.2019.01.014
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Pagination
554-572.e7Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.