PUBLICATION
Precise Cellular Ablation Approach for Modeling Acute Kidney Injury in Developing Zebrafish
- Authors
- Datta, R., Wong, A., Camarata, T., Tamanna, F., Ilahi, I., Vasilyev, A.
- ID
- ZDB-PUB-170613-2
- Date
- 2017
- Source
- Journal of visualized experiments : JoVE (124): (Journal)
- Registered Authors
- Vasilyev, Aleksandr
- Keywords
- none
- MeSH Terms
-
- Acute Kidney Injury/etiology*
- Animals
- Disease Models, Animal*
- Green Fluorescent Proteins/genetics
- Laser Therapy*
- Nephrons/physiology
- Pronephros/metabolism
- Zebrafish/embryology
- PubMed
- 28605371 Full text @ J. Vis. Exp.
Citation
Datta, R., Wong, A., Camarata, T., Tamanna, F., Ilahi, I., Vasilyev, A. (2017) Precise Cellular Ablation Approach for Modeling Acute Kidney Injury in Developing Zebrafish. Journal of visualized experiments : JoVE. (124).
Abstract
Acute Kidney Injury (AKI) is a common medical condition with a high mortality rate. With the repair abilities of the kidney, it is possible to restore adequate kidney function after supportive treatment. However, a better understanding of how nephron cell death and repair occur on the cellular level is required to minimize cell death and to enhance the regenerative process. The zebrafish pronephros is a good model system to accomplish this goal because it contains anatomical segments that are similar to the mammalian nephron. Previously, the most common model used to study kidney injury in fish was the pharmacological gentamicin model. However, this model does not allow for precise spatiotemporal control of injury, and hence it is difficult to study cellular and molecular processes involved in kidney repair. To overcome this limitation, this work presents a method through which, in contrast to the gentamicin approach, a specific Green Fuorescent Protein (GFP)-expressing nephron segment can be photoablated using a violet laser light (405 nm). This novel model of AKI provides many advantages that other methods of epithelial injury lack. Its main advantages are the ability to "dial" the level of injury and the precise spatiotemporal control in the robust in vivo animal model. This new method has the potential to significantly advance the level of understanding of kidney injury and repair mechanisms.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping