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Ex vivo culture of isolated zebrafish whole brain.
Tomizawa, K; Kunieda, J; Nakayasu, H.
Affiliation
  • Tomizawa K; Department of Biology, Faculty of Science, Okayama University, 700-8530, Okayama, Japan.
J Neurosci Methods ; 107(1-2): 31-8, 2001 May 30.
Article in En | MEDLINE | ID: mdl-11389939
ABSTRACT
We have succeeded in culturing whole zebrafish brains ex vivo for 1 week. While isolated cells and tissue slices have previously been employed for neurobiological studies, these techniques are limited, because while local networks may be preserved, their original context in the whole brain is lost. Culture of the whole brain would facilitate the study of cells and systems within an intact brain infrastructure. Our culture method entailed isolating the whole brain and placing it on a sterile and porous membrane, after which it was maintained with a conditioned medium in a six-well plate in a CO2 incubator at 28.5 degrees C. Whole brains cultured by this simple method were relatively unaltered in terms of their morphology, cytoarchitecture, immunohistochemistry and ability to transport horse radish peroxidase (HRP). This method of cultivation may be very useful for neurobiological research.
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Collection: 01-internacional Database: MEDLINE Main subject: Organ Culture Techniques / Zebrafish / Brain Limits: Animals Language: En Journal: J Neurosci Methods Year: 2001 Document type: Article Affiliation country: Japón
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Organ Culture Techniques / Zebrafish / Brain Limits: Animals Language: En Journal: J Neurosci Methods Year: 2001 Document type: Article Affiliation country: Japón