Long-term bidirectional neuron interfaces for robotic control, and in vitro learning studies

There are two fundamentally different goals for neural interfacing. On the biology side, to interface living neurons to external electronics allows the observation and manipulation of neural circuits to elucidate their fundamental mechanisms. On the engineering side, neural interfaces in animals, people, or in cell culture have the potential to restore missing functionality, or someday, to enhance existing functionality. At the Laboratory for NeuroEngineering at Georgia Tech, we are developing new technologies to help make both goals attainable. We culture dissociated mammalian neurons on multielectrode arrays, and use them as the brain of a 'Hybrot', or hybrid neural-robotic system. Distributed neural activity patterns are used to control mobile robots. We have created the hardware and software necessary to feed the robots' sensory inputs back to the cultures in real time, as electrical stimuli. By embodying cultured networks, we study learning and memory at the cellular and network level, using 2-photon laser-scanning microscopy to image plasticity while it happens. We have observed a very rich dynamical landscape of activity patterns in networks of only a few thousand cells. We can alter this landscape via electrical stimuli, and use the hybrot system to study the emergent properties of networks in vitro.

[1]  Aude Billard,et al.  From Animals to Animats , 2004 .

[2]  G. Bi,et al.  Synaptic Modifications in Cultured Hippocampal Neurons: Dependence on Spike Timing, Synaptic Strength, and Postsynaptic Cell Type , 1998, The Journal of Neuroscience.

[3]  D. McFarland,et al.  Artificial Ethology , 2001 .

[4]  Steve M. Potter Vital imaging: Two photons are better than one , 1996, Current Biology.

[5]  H. Robinson,et al.  Simultaneous induction of pathway-specific potentiation and depression in networks of cortical neurons. , 1999, Biophysical journal.

[6]  P. Laming,et al.  Glial cells : their role in behaviour , 1998 .

[7]  Steve M. Potter,et al.  High-speed CCD movie camera with random pixel selection for neurobiology research , 1997, Other Conferences.

[8]  Steve M. Potter,et al.  A new approach to neural cell culture for long-term studies , 2001, Journal of Neuroscience Methods.

[9]  M. Nicolelis,et al.  Reconstructing the Engram: Simultaneous, Multisite, Many Single Neuron Recordings , 1997, Neuron.

[10]  B M Salzberg,et al.  A large change in axon fluorescence that provides a promising method for measuring membrane potential. , 1973, Nature: New biology.

[11]  E M Callaway,et al.  Brominated 7-hydroxycoumarin-4-ylmethyls: photolabile protecting groups with biologically useful cross-sections for two photon photolysis. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[12]  Daniel A. Wagenaar,et al.  The Neurally Controlled Animat: Biological Brains Acting with Simulated Bodies , 2001, Auton. Robots.

[13]  Stanley J. Rosenschein,et al.  From Animals to Animats: Proceedings of the First International Conference on Simulation of Adaptive Behavior , 1996 .

[14]  H. Robinson,et al.  Spontaneous periodic synchronized bursting during formation of mature patterns of connections in cortical cultures , 1996, Neuroscience Letters.

[15]  William Bialek,et al.  Spikes: Exploring the Neural Code , 1996 .

[16]  Steve M. Potter,et al.  Distributed Processing in Cultured Neuronal Networks Chapter 4 , 2001 .

[17]  Steve M. Potter,et al.  Real-time multi-channel stimulus artifact suppression by local curve fitting , 2002, Journal of Neuroscience Methods.

[18]  P. Saggau,et al.  High-speed, random-access fluorescence microscopy: II. Fast quantitative measurements with voltage-sensitive dyes. , 1999, Biophysical journal.