Modeling neurodegenerative diseases in zebrafish embryos

Angela S. Laird, Wim Robberecht*

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapter

7 Citations (Scopus)

Abstract

Although the zebrafish (Danio rerio) has been used extensively for many years in neurodevelopmental studies, use of this teleost to study neurological diseases has evolved only recently. Being a vertebrate, this animal offers advantages for the study of human disease over other small animals, such as the fly or worm. Genetic, as well as nongenetic, disorders can be modeled in both the adult organism and the embryo. Genetic manipulation of the embryo to generate stable and transiently expressing transgenic fish, and to knockdown genes to study loss of their function, can be easily achieved. Because of large offspring numbers screening studies can also be readily performed. Here, we describe some of the protocols useful for modeling neurodegenerative disease in zebrafish embryos, with particular emphasis on models to study motor neuron phenotypes.

Original languageEnglish
Title of host publicationNeurodegeneration
Subtitle of host publicationMethods and Protocols
EditorsGiovanni Manfredi, Hibiki Kawamata Fujita
Place of PublicationTotowa, NJ
PublisherHumana Press
Pages167-184
Number of pages18
ISBN (Electronic)9781617793288
ISBN (Print)9781617793271
DOIs
Publication statusPublished - 2011
Externally publishedYes

Publication series

NameMethods in Molecular Biology
PublisherHumana Press
Volume793
ISSN (Print)1064-3745

Fingerprint Dive into the research topics of 'Modeling neurodegenerative diseases in zebrafish embryos'. Together they form a unique fingerprint.

Cite this