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Vol. 7, No. 6, pp. 383-392, November/December 2000
1 Department of Integrative Physiology, Graduate School of
Medical Sciences Kyushu University, Fukuoka 812-8582
Japan; 2 Department of Pathology, Osaka University Graduate
School of Medicine, Suita 565 Japan
The c-kit receptor tyrosine kinase encoded by the
white-spotting (W) gene is highly expressed in rat
hippocampal CA1-CA4 regions. We found an impaired spatial learning and
memory in homozygous c-kit (Ws/Ws) mutant
rats that have a 12-base deletion in the tyrosine kinase domain of the
c-kit gene and a very low kinase activity.
Electrophysiological studies in hippocampal slices revealed that the
long-term potentiation (LTP) induced by the tetanic stimulation (100 Hz, 1 sec) in the mossy fiber (MF)-CA3 pathway, but not in the
Schaffer collaterals/commissural-CA1 pathway, was significantly reduced in c-kit mutants compared with wild-type (+/+) rats.
The paired-pulse facilitation (PPF) was measured before the tetanus and
after the establishment of the LTP in each slice. The initial PPF in
the MF-CA3 pathway positively correlated with the amplitude of the LTP
in the wild-type rats but not in the c-kit mutant rats. Furthermore, they failed to show the normal characteristics observed in
the MF-CA3 pathway of +/+ rats; that is, the negative correlation between the initial PPF and the changes in PPF measured after the LTP.
These findings suggest an involvement of SCF/c-kit signaling in hippocampal synaptic potentiation and spatial learning and memory.
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