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Haruo Kasai
National Institute of Physilogical
Sciences, Okazaki, Japan
The Kasai Lab was the first to accomplish diffraction
limited 2-photon photolysis of caged glutamate,
which was developed in our lab. Using focal uncaging
from MNI-Glu, they have been able to mimic quantal
release, the fundamental chemical synaptic event
in the CNS. Using this approach, they have developed
techniques for producing maps of receptors in
living cells (see below). Our work together is
supported by a R24 grant from the National Institute
of General Medical Sciences (only the 3rd such
grant ever awarded), and by a Program Grant from
the Human
Frontiers Science Program (with Martin
Bootman-this grant was ranked 11th out of
634 applicants.)

2D projections of 3D images of postsynaptic
dendritic volume in CA1 neurons in slices
and the AMPA-R density imaged by 2-photon
photolysis of MNI-Glu in that space. Lateral
and axial resolution of mapping are shown
right. These results were reported in Nature
Neuroscience (2001), 4, 1086.
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The Kasai lab have now applied this 2-photon
mapping technique to image long-term potentiation
at single dendritic spine heads in CA1 hippocampal
neurons in brain slices. They have shown definitely
that Hebb's learning principle can apply to a
single synapse, ie. they combine simultaneous
postsynaptic depolarization with brief photochemical
tetanus (720 nm, 2 Hz for 1 min, 5 mW per uncaging
event), to induce profound morphological plasticity
(upper panel shows fluorescent images of eGFP-filled
dendrites imaged at 910 nm). These technically
challenging experiments with their dual 2-photon
microscope permit receptor imaging at normal resting
potentials (over a period of more than 80 mins).
These results have been published in Nature
(2004) 429, 761).


I visited the Kasai lab in November 2004. We
spent 4 days looking at Zen temples in
Kyoto (An account of my trip with many
photos is here). We did some work too (honest).
Here I am with Kasai and Masanori Matsuzaki (left),
and with Masanori and Jun Noguchi (right).
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