The 64th JSAP Spring Meeting, 2017

Presentation information

Symposium (Oral)

Symposium » English session: Joint Symposium on Nanobiotechnology and Biosensing

[15p-313-1~10] English session: Joint Symposium on Nanobiotechnology and Biosensing

Wed. Mar 15, 2017 1:15 PM - 6:30 PM 313 (313)

Hiroaki Takehara(Univ. of Tokyo), Ayumi Hirano(Tohoku Univ.), Koichiro Miyamoto(Tohoku Univ.)

5:45 PM - 6:15 PM

[15p-313-9] Dissociated neuronal culture coupled to micro-electrode array: measurement of the network dynamics and application toward neural interface

Daisuke Ito1,2, Kazutoshi Gohara3, Michela Chiappalone1 (1.Italian Inst. Tech., 2.JSPS, 3.Hokkaido Univ.)

Keywords:microelectrode array, cultured neuronal network

Primary neuronal cultures dissociated from different regions of the central nervous system have been a classical model for in vitro studies of neurobiological mechanisms. Developed at the beginning of the 80’s, the Micro-Electrode Array (MEA) technique nowadays offers a useful experimental approach for in vitro electrophysiological investigations. Previous work demonstrated the possibility to use dissociated neuronal networks coupled to MEAs as a cell-based biosensor.
Here, we present our recent studies using neuronal culture coupled to MEAs: 1) principal properties of cultured neuronal networks revealed by long-term measurement of spatiotemporal dynamics. 2) development of neuronal network cultured on graphene-transferred MEAs. 3) neuronal cultures embodied in a closed-loop environment.
Primary neurons cultured on MEAs autonomously formed functional networks, after elongating axons and establishing synaptic connections. The neuronal networks showed spontaneous uncorrelated firing within several days; the spontaneous spikes became synchronized bursts as the network grew. The quantified activity as mean firing rate and bursting rate showed an initial increase and subsequent saturation during the 1-month culture period. As a result of quantification of synaptic density by immunostaining, it was clarified that the number of culture days to saturation from the initial increase in synaptic density corresponded to the electrical activity. In addition, we found the specific gene expression corresponded to the maturation of neuronal network.
Then, we present the study on the neuronal network cultured on graphene-transferred MEAs. As it has been widely known, graphene is a thin layer of pure carbon; it is a single, tightly packed layer of carbon atoms bonded together in a hexagonal lattice. We transferred single-wall graphene to MEA substrate and attempt to culture primary neuronal cells on the substrate. Interestingly, the culture on graphene-transferred MEAs showed higher number of spikes compared to conventional condition.
Finally, we present a new hybrid neuro-robotic architecture based on a neural controller bi-directionally connected to a virtual robot implementing a Braitenberg vehicle aimed at avoiding obstacles. The robot is characterized by proximity sensors and wheels, allowing it to navigate into a circular arena with obstacles of different sizes. As neural controller, we used neuronal cultures. These study offers a new framework for studying, in simplified model system, neuro-artificial bi-directional interfaces for the development of new strategies for brain-machine interaction.