header logo image header logo text
Downloads Login
Research
General Information
ZIRC
ZFIN ID: ZDB-PUB-170928-19
Intravital imaging of metastasis in adult Zebrafish
Benjamin, D.C., Hynes, R.O.
Date: 2017
Source: BMC cancer 17: 660 (Journal)
Registered Authors:
Keywords: Intravital imaging, Metastasis, Zebrafish
MeSH Terms:
  • Animals
  • Cell Line, Tumor
  • Disease Models, Animal
  • Humans
  • Intravital Microscopy/methods*
  • Melanoma/diagnostic imaging*
  • Melanoma/pathology
  • Mice
  • Microscopy, Confocal
  • Neoplasm Metastasis
  • Zebrafish
PubMed: 28946867 Full text @ BMC Cancer
FIGURES
ABSTRACT
Metastasis is a major clinical problem whose biology is not yet fully understood. This lack of understanding is especially true for the events at the metastatic site, which include arrest, extravasation, and growth into macrometastases. Intravital imaging is a powerful technique that has shown great promise in increasing our understanding of these events. To date, most intravital imaging studies have been performed in mice, which has limited its adoption. Zebrafish are also a common system for the intravital imaging of metastasis. However, as imaging in embryos is technically simpler, relatively few studies have used adult zebrafish to study metastasis and none have followed individual cells at the metastatic site over time. The aim of this study was to demonstrate that adult casper zebrafish offer a convenient model system for performing intravital imaging of the metastatic site over time with single-cell resolution.
ZMEL1 zebrafish melanoma cells were injected into 6 to 10-week-old casper fish using an intravenous injection protocol. Because casper fish are transparent even as adults, they could be imaged without surgical intervention. Individual cells were followed over the course of 2 weeks as they arrested, extravasated, and formed macroscopic metastases.
Our injection method reliably delivered cells into circulation and led to the formation of tumors in multiple organs. Cells in the skin and sub-dermal muscle could be imaged at high resolution over 2 weeks using confocal microscopy. Arrest was visualized and determined to be primarily due to size restriction. Following arrest, extravasation was seen to occur between 1 and 6 days post-injection. Once outside of the vasculature, cells were observed migrating as well as forming protrusions.
Casper fish are a useful model for studying the events at the metastatic site using intravital imaging. The protocols described in this study are relatively simple. Combined with the reasonably low cost of zebrafish, they offer to increase access to intravital imaging.
ADDITIONAL INFORMATION