[Opt Bio] Year Started : 2018

Fumitaka Osakada

Four-dimensional optical technologies for revealing and manipulating highly specific neural circuits

Research Director
Fumitaka Osakada

Associate Professor
Graduate School of Pharmaceutical Sciences
Nagoya University

Collaborator
Keisuke Isobe Senior Scientist
Center for Advanced Photonics
RIKEN
Outline

The brain is a complex and dynamic structure composed of heterogeneous neuronal populations synaptically connected with each other. Our goal is to understand how neural circuits perform computations that generate perception and memory. We aim to reveal the structure and function of neural circuits, dissect circuit computations, and manipulate neuronal activities of circuit components at the individual cell level during sensation and behavior, by developing four-dimensional optical methods combined with genetic and viral technologies.

Erina Kuranaga

Establishment of technologies for “all-optical mechanobiology” and its application to developmental biology.

Research Director
Erina Kuranaga

Professor
Graduate School of Life Sciences
Tohoku University

Collaborator
Yasushi Okada Professor
The University of Tokyo
Erina Kuranaga Professor
The University of Kyoto
Tatsuo Shibata Team Leader
Center for Biosystems Dynamics Research
RIKEN
Tomonobu M Watanabe Team Leader
Center for Biosystems Dynamics Research
RIKEN
Outline

Mechanobiology is an emerging field of science that focuses on how physical forces influence biological processes over time. Its potential application includes developmental engineering and regenerative medicine. However, mechanobiological studies of cells in tissues or in vivo have been difficult due to the lack of non-invasive methods for measurement and perturbation. In this project, we aim to establish “all-optical mechanobiology” by developing the optical techniques to measure and manipulate the mechanical properties of the cells and to observe their biological responses.

Masayuki Matsumoto

Elucidation and reconstruction of dopamine functions by optogenetic approaches in nonhuman primates

Research Director
Masayuki Matsumoto

Professor
Faculty of Medicine
University of Tsukuba

Collaborator
Masahiko Takada Researcher
Center for the Evolutionary Origins of Human Behavior
Kyoto University
Satomi Chiken Assistant Professor
National Institute for Basic Biology
National Institutes of Natural Sciences
Outline

Dysfunctions of the dopamine system cause multiple impairments such as motor, cognitive and motivational impairments as seen in patients with Parkinson’s disease. In this research, we develop optogenetic methodologies that can manipulate the activity of the dopamine system in the monkey brain as a model for similar systems in the human brain. Using the optogenetic methodologies, we then elucidate the mechanism how the dopamine system regulates diverse functions in the primate brain. We also develop optogenetic approaches to reconstruct functions of the impaired dopamine system in monkey models. This research provides more mechanistic accounts of symptoms in neurological/psychiatric disorders with dopaminergic dysfunctions, and new approaches to treat the disorders.

Michisuke Yuzaki

New optogenetic tools to decipher synaptic plasticity underlying learning and memory in vivo

Research Director
Michisuke Yuzaki

Professor
School of Medicine
Keio University

Collaborator
Itaru Hamachi Professor
Graduate School of Engineering
Kyoto University
Shinji Matsuda Associate Professor
Graduate School of Informatics and Engineering
The University of Electro-Communications
Outline

Neuronal activity-induced changes in the efficacy of synapses, known as long-term potentiation (LTP) and long-term depression (LTD), are observed in diverse neural circuits and thought to underlie the storage of information acquired during learning. However, whether LTP/LTD at specific synapses is directly and causally linked to learning and memory in vivo remains incompletely understood. In this proposal, we will address this question by developing new optogenetic tools that can directly and reversibly regulate LTP/LTD in vivo.

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