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2015 Fiscal Year Final Research Report

Molecular and physiological mechanisms of the cerebellar compartmentalization

Research Project

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Project/Area Number 25430008
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Neurophysiology / General neuroscience
Research InstitutionFukushima Medical University (2015)
Nagoya University (2013-2014)

Principal Investigator

Hashimoto Mitsuhiro  福島県立医科大学, 医学部, 助教 (90311357)

Project Period (FY) 2013-04-01 – 2016-03-31
Keywords小脳 / アデノウイルスベクター / 神経細胞の誕生日 / 22q13欠失症候群 / Wnt7b
Outline of Final Research Achievements

1. We newly generated an adenoviral vector expressing antisense RNA of Wnt7b. The adenoviral vector suppressed successfully Wnt7b-expression in vitro and in vivo. Using the adenoviral vector, we suppressed Wnt7b-expression in neurons born on embryonic day (E)11.5, selectively. Wnt7b-suppression caused underdevelopment, neocortex hypoplasia, cerebellar vermis hypoplasia, autism-like abnormal behavior, and abnormal EEG.
2. We newly made two kinds of optical-stimulators that were small enough to mount the device on a mouse head.One was controlled by infrared wireless communication and another one was controlled bywireless communication of Bluetooth 4.0 (Bluetooth Low Energy) . The Bluetooth-device could be modulated by an iPad or iPhone application.

Free Research Field

神経科学

URL: 

Published: 2017-05-10  

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