Graduate School of Frontier Biosciences, Osaka University

Japanese

Cellular and Molecular Neurobiology Group

  Name Email TEL
Professor YAMAMOTO, Nobuhiko, Ph.D. +81-6-6879-4636
Associate Prof. SHIRASAKI,Ryuichi, Ph.D. +81-6-6879-4635
Assistant Prof. SUGO, Noriyuki , Ph.D. +81-6-6879-4635
TEL +81-6-6879-4637
FAX +81-6-6879-4636
Postal Mail Address Cellular and Molecular Neurobiology Group,
Graduate School of Frontier Biosciences, Osaka University,
1-3 Yamadaoka, Suita, Osaka 565-0871, Japan
for more infomation http://www.fbs.osaka-u.ac.jp/labs/neurobiol/NYstudye.html
We are interested in how neuronal connections are formed during development of the brain. It has been suggested that fundamental patterns of neuronal circuits are established by a precise developmental program whereas fine connections are modified by electrical activity including spontaneous firing. We are exploring cellular and molecular mechanisms that underlie these processes, focusing on neocortical connections.

1. Laminar specific connectionsLaminar specific connections

20_img1.gifOne of the characteristic features in cortical connections is layer specificity. The neocortex is composed of six cell layers, by which extrinsic and intrinsic cortical connections are organized. In particular the thalamocortical projection is well characterized in terms of laminar specificity and development. During development sensory thalamocortical axons travel through the specific pathways, enter the cortical plate, pass through the deep cortical layers and finally project to layer 4. How thalamocortical axons recognize the target layer? Previous in vitro studies with organotypic coculture preparations have demonstrated that thalamic axons exhibit stopping and branching behavior in the target layer. Moreover, evidence indicates that stopping is attributable to the inhibitory activity (partly due to glycosylphosphatidylinositol-linked molecules) in the upper cortical layers, whereas lamina-specific branching is regulated by a positive factor (unknown) in the target layer and an inhibitory component (polysialylated neural cell adhesion molecule) in all cortical layers. To reveal the molecular mechanisms that are responsible for axonal stopping and branching behaviors, we attempt to identify the genes that are expressed specifically in layer 4 or in the upper layers.

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