Publication: Studying the Fate of Tumor Extracellular Vesicles at High Spatiotemporal Resolution Using the Zebrafish Embryo.
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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.
Description
We thank all members of the Goetz Lab for helpful discussions. We are indebted to K. Richter and F. Peri (EMBL, Heidelberg, Germany) as well as to P. Hanns and C. Lengerke (University Hospital Basel, Switzerland) for supplying zebrafish embryos. We are grateful to R. White (MSKCC, New York, USA) for the Zmel1 (native and tdTomato) cells, to Dr. D.C. Bennett (St. George's University of London, U.K.) and Dr. M. Soengas (CNIO, Madrid, Spain) for mammalian melanoma cells, and to P. Zimmerman (CRCM, Marseille, France) for the Syntenin-2 construct. We thank A. Michel (EFS, Strasbourg, France) and C. Spiegelhalter (IGBMC, Illkirch, France) for EM assistance, Y. Schwab for advice during CLEM analysis (EMBL, Heidelberg), E. Guiot and Y. Lutz (IGBMC, Illkirch, France) for advice on confocal imaging, and A. Audfray (Malvern Instruments) for NTA. We thank the CNIO proteomics core for performing the mass spectrometry on mouse and human melanoma EVs. We thank P. Herbomel for critical reading of the manuscript. This work was supported by a fellowship from IDEX (University of Strasbourg) to S.G.; by grants from La Ligue contre le Cancer, Canceropole Grand-Est, INCa (MetaCLEM) and Roche to J.G.G.; and by institutional funds from University of Strasbourg, INSERM, and ANR (to CC, French Proteomics Infrastructure ProFI; ANR-10-INBS-08-03).





