RESEARCH
Peer reviewed scientific video journal
Video encyclopedia of advanced research methods
Visualizing science through experiment videos
EDUCATION
Video textbooks for undergraduate courses
Visual demonstrations of key scientific experiments
BUSINESS
Video textbooks for business education
OTHERS
Interactive video based quizzes for formative assessments
Products
RESEARCH
JoVE Journal
Peer reviewed scientific video journal
JoVE Encyclopedia of Experiments
Video encyclopedia of advanced research methods
EDUCATION
JoVE Core
Video textbooks for undergraduates
JoVE Science Education
Visual demonstrations of key scientific experiments
JoVE Lab Manual
Videos of experiments for undergraduate lab courses
BUSINESS
JoVE Business
Video textbooks for business education
Solutions
Language
English
Menu
Menu
Menu
Menu
Zebrafish embryo xenografts are useful in studying cancer cell invasion. Prepare xenograft models by injecting fluorescently labeled metastatic cancer cells and non-cancerous cells into the perivitelline space of two transgenic embryos. The perivitelline space is a space between the embryo periderm and the yolk sac. Let embryos grow for the desired period.
During this period, metastatic cancer cells divide aggressively in the injection site while non-cancerous cells remain stable. After incubation, use a pasteur pipette to transfer embryos into a glass bottom suspension dish. Remove excess egg water and position embryos in the desired position for imaging. Keep a cover slip on top of the dish and place the dish under a bright field microscope.
Capture images and analyze the invasive behavior of both types of cells. Metastatic cancer cells tend to invade blood vessels from the injection site. They move along the circulation, and then invade into the surrounding tissue to proliferate. In contrast, the non-cancerous cells remain at the site of injection. In the example protocol, we will inject breast cancer cells into the perivitelline space and duct of Cuvier in zebrafish xenograft models to study metastasis.
To visualize metastasis, with a pasteur pipette, transfer the injected zebrafish embryo to a glass bottom polystyrene dish and remove excess egg water. Image the whole body of the embryo with a confocal microscope set to low magnification to obtain a general pattern of tumor cell dissemination.
Use a 488 nanometer laser to visualize the zebrafish embryo vasculature and a 543 nanometer laser to visualize implanted tumor cells labeled with red fluorescent marker. Next, scan the embryo in eight to ten steps to acquire a high quality image.
Related Videos
08:15
Related Videos
16.2K Views
12:03
Related Videos
12.7K Views
07:31
Related Videos
12.4K Views
03:56
Related Videos
2K Views
11:39
Related Videos
8K Views
09:22
Related Videos
17.2K Views
11:07
Related Videos
7.3K Views
09:50
Related Videos
8.4K Views
12:08
Related Videos
13.3K Views
05:20
Related Videos
3K Views