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Generation of Transgenic Rats using a Lentiviral Vector Approach
Published on: May 17, 2020
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Transgenic rats for tracking body fluid/tissue-derived extracellular vesicles
Aya Yoshimura1, Yoshitaka Tamai2, Takahiro Ochiya3
1Education and Research Center of Animal Models for Human Diseases, Fujita Health University, Toyoake, Aichi, Japan.
Methods in Enzymology
|February 10, 2021
Summary
Researchers developed methods to track extracellular vesicles (EVs) in vivo using CD63-GFP transgenic rats. This allows for better understanding of EV communication and biogenesis in body fluids and brains.
Area of Science:
- Biochemistry
- Cell Biology
- Neuroscience
Background:
- Extracellular vesicles (EVs) are key mediators of intercellular communication.
- In vivo visualization of EVs is crucial for understanding their biogenesis and function.
- The tetraspanin CD63 is a common marker for EVs and can be fluorescently tagged for tracking.
Purpose of the Study:
- To develop and present methods for isolating and tracking extracellular vesicles (EVs) in vivo.
- To utilize transgenic rats expressing CD63-GFP for enhanced EV visualization.
- To investigate EV transfer and biogenesis in body fluids and brain tissue.
Main Methods:
- Generation of transgenic rats expressing CD63-GFP in body fluids and brain.
- Isolation of extracellular vesicles (EVs) from various biological samples.
- Development of in vivo assays for EV tracking and transfer analysis.
Main Results:
- Successful isolation of CD63-GFP labeled EVs from transgenic rat body fluids and brains.
- Demonstration of EV transfer and communication pathways in vivo.
- Validation of CD63-GFP as a reliable marker for in vivo EV studies.
Conclusions:
- Transgenic rats expressing CD63-GFP provide a valuable tool for in vivo extracellular vesicle (EV) research.
- The developed assays facilitate the study of EV biogenesis, trafficking, and intercellular communication.
- This approach enhances our ability to visualize and understand EV roles in physiological and pathological processes.

