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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The aim of this method is to generate an in vivo model of tumor angiogenesis by xenografting mammalian tumor cells into a zebrafish embryo that has fluorescently-labelled blood vessels. By imaging the xenograft and associated vessels, a quantitative measurement of the angiogenic response can be obtained.

Abstract

Tumor angiogenesis is a key target of anti-cancer therapy and this method has been developed to provide a new model to study this process in vivo. A zebrafish xenograft is created by implanting mammalian tumor cells into the perivitelline space of two days-post-fertilization zebrafish embryos, followed by measuring the extent of the angiogenic response observed at an experimental endpoint up to two days post-implantation. The key advantage to this method is the ability to accurately quantitate the zebrafish host angiogenic response to the graft. This enables detailed examination of the molecular mechanisms as well as the host vs tumor contribution to the angiogenic response. The xenografted embryos can be subjected to a variety of treatments, such as incubation with potential anti-angiogenesis drugs, in order to investigate strategies to inhibit tumor angiogenesis. The angiogenic response can also be live-imaged in order to examine more dynamic cellular processes. The relatively undemanding experimental technique, cheap maintenance costs of zebrafish and short experimental timeline make this model especially useful for the development of strategies to manipulate tumor angiogenesis.

Introduction

Angiogenesis is one of the classic hallmarks of cancer and represents a target of anti-cancer therapy1,2. To study this process, xenograft models of cancer have been created by implanting mammalian tumor cells into animals such as mice3. A zebrafish xenograft model has also been developed, which involves the implantation of tumor cells into 2 days post fertilization (dpi) zebrafish which results in rapid growth of zebrafish blood vessels into the xenograft4.

This protocol describes an in vivo zebrafish embryo tumor xenograft model in w....

Protocol

1. Preparation of Microinjection Needles

  1. Turn on a micropipette puller and set the following parameters (calibrated for the micropipette puller model listed in Table of Materials): Heat, 680; Pull, 75; Velocity, 40; Time, 55; Pressure: 530.
  2. Secure a borosilicate glass capillary into the micropipette puller and pull the capillary to make two needles. Repeat for as many needles as desired.

2. Cell Culture for Implantation

Representative Results

By imaging an individual xenograft at 6, 24 and 48 hpi, the angiogenic response at different timepoints can be calculated as shown in Figure 1A-C. The largest angiogenic response is observed between 24-48 h post implantation, with the maximum levels of graft vascularization seen around 2 dpi (Figure 1A-C). A time-lapse movie of a typical angiogenic response to a B16-F1 xenograft from 20.75 hpi un.......

Discussion

The first critical step in the protocol is the implantation of tumor cells. It is essential that cells are injected into a location that will allow the xenograft to implant successfully in the embryo without making the embryo edematous. An injection that is too anterior can allow the cells to move towards the heart, blocking the bloodstream and leading to edema, while an injection that is too posterior will result in a poorly implanted xenograft. An anterior injection is best avoided by inserting the needle through the y.......

Acknowledgements

We thank Mr. Alhad Mahagaonkar for managing the University of Auckland zebrafish facility and the Biomedical Imaging Research Unit, School of Medical Sciences, University of Auckland, for assistance in time-lapse confocal microscopy. This work was supported by a Health Research Council of New Zealand project grant (14/105), a Royal Society of New Zealand Marsden Fund Project Grant (UOA1602) and an Auckland Medical Research Foundation Project Grant (1116012) awarded to J.W.A.

....

Materials

NameCompanyCatalog NumberComments
Air cylinderBOC011GXenotransplantation
B16-F1 cellsATCCCell culture
BD Matrigel LDEV-free (extracellular matrix mixture)Corning356235Xenotransplantation
Borosillicate glass capillariesWarner InstrumentsG100T-4OD=1.00 mm, ID=0.78 mm, Length =10 cm Cell injection
Cell culture dish -35 mm diameterThermofisher NZNUN153066Fish husbandry
Cell culture dish -100 mm diameterSigma-AldrichCLS430167-500EAFish husbandry
Cell culture flask 75 cm2In Vitro TechnologiesCOR430641Cell culture
CellTracker GreenInvitrogenC2925Cell labelling, Stock concentration (10 mM in DMSO), working concentration (0.2 μM in serum-free media)
Dimethyl sulfoxideSigma-AldrichD8418Drug treatment, Cell labelling
E3 Media (60x in 2 L of water) 34.8 g NaCl

1.6 g KCl

5.8 g CaCl2·2H2O

9.78 g MgCl2·6H2O adjust to pH 7.2 with NaOH
In house [1]Fish husbandry
Ethyl-3-aminobenzoate methanesulfonate (Tricaine)Sigma-AldrichE10521Xenotransplantation, Imaging
Filter tip 1000 μLVWR732-1491Used during multiple steps
Filter tip 200 μLVWR732-1489Used during multiple steps
Filter tip 10 μLVWR732-1487Used during multiple steps
Fluorescence microscopeLeicaMZ16FAPreparation of embryos
FBS (NZ origin)Thermofisher Scientific10091148Cell culture
GlovesAny commercial brandUsed during multiple steps
Haemocytometer cell counting chamber Improved NeubauerHawksleyVetAC1000Xenotransplantation
Heraeus Multifuge X3R CentrifugeThermofisher Scientific75004500Cell culture, Cell labelling
Hoechst 33342Thermofisher Scientific62249Cell labelling, Stock concentration (1 mg/ml in DMSO), working concentration (6 μg/ml in serum-free media)
Low Melting Point, UltraPure AgaroseThermofisher Scientific16520050Imaging
MethycelluloseSigma-Aldrich9004 67 5Xenotransplantation
Methylene bluesigma-AldrichM9140Fish husbandry
Microloader 0.5-20 μL pipette tip for loading microcapillariesEppendorf5242956003Xenotransplantation
MicropipettesAny commercial brandUsed during multiple steps
Micropipette puller P 87Sutter InstrumentsXenotransplantation
Microscope cage incubatorOkolabTime-lapse imaging
MicrowaveAny commercial brandImaging
Mineral oilSigma-AldrichM3516Xenotransplantation
Minimal Essential Media (MEM) - alphaThermofisher Scientfic12561056Cell Culture
MPPI-2 Pressure InjectorApplied Scientific InstrumentationXenotransplantation
Narishige micromanipulatorNarishige GroupXenotransplantation
Nikon D Eclipse C1 Confocal MicroscopeNikonImaging
N-Phenylthiourea (PTU)Sigma-AldrichP7629Fish husbandry
PBSGibco10010023Cell culture
Penicillin StreptomycinLife Technologies15140122Cell culture
S1 pipet fillerThermoscientific9501Cell culture
Serological stripette 10 mLCorning4488Cell culture
Serological stripette 25 mLCorning4489Cell culture
Serological stripette 5 mLCorning4485Cell culture
Serological stripette 2 mLCorning4486Cell culture
Terumo Needle 22 gaugeAmtechSH 182Fish husbandry
Tissue culture incubatorThermofisher ScientficHeraCell 150iCell culture
Tivozanib (AV951)AVEO PharmaceuticalsDrug treatment
Transfer pipette 3 mLMedirayRL200CFish husbandry
Trypsin/EDTA (0.25% )Life TechnologiesT4049Cell culture
TweezersFine Science Tools11295-10Fish husbandry
Volocity Software (v6.3)Improvision/Perkin ElmerImage analysis

References

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In Vivo ImagingTumor XenograftsZebrafishAngiogenesisVascularizationQuantitationB16 F1 CellsMicroinjectionTransgenic EmbryosECMYolk Sac

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