Journal of Neuroscience, Vol 8, 1929-1939, Copyright © 1988 by Society for Neuroscience
Spatial distribution of Ca currents in molluscan neuron cell bodies and regional differences in the strength of inactivation
S Thompson and J Coombs
Hopkins Marine Station, Stanford University, Pacific Grove, California 93950.
The spatial distribution of Ca current in molluscan neuron cell bodies was
studied using a large patch method in combination with 2- microelectrode
voltage clamp. The method has a spatial resolution equal to about 0.1% of
the cell body area. Ca current is not uniformly distributed. The current
density varies between patches, changing by as much as a factor of 2.5 over
a distance of 20 micron, and there is evidence that Ca current occurs in
"hot spots" involving a few hundred channels. The current density increases
in a moderately steep gradient from the soma cap, opposite the axon, toward
the axon hillock. Ca currents in patches from different regions of the soma
are qualitatively different. Currents near the soma cap do not inactivate
or inactivate weakly during depolarization, while currents of equal density
nearer the axon hillock exhibit pronounced inactivation. The strength of
inactivation increases in parallel with the gradient in current density,
but local differences in current density, or in the number of active Ca
channels, do not explain the variability in inactivation. Inactivating and
noninactivating Ca currents could not be distinguished on the basis of
activation or deactivation kinetics, voltage dependence of activation, or
sensitivity to hyperpolarizing conditioning pulses. Also, the amplitude of
noninactivating current near the soma cap is reduced by intracellular Ca
injection showing that, like the whole-cell current, Ca current in this
region is subject to Ca-dependent inactivation. The data favor the
hypothesis that these cells express only one type of Ca channel.
Differences in the strength of inactivation may result from local
differences in cytoplasmic Ca buffering, local modification of Ca channels
in a way that changes their sensitivity to Ca-dependent inactivation, or
local differences in the availability of cytoplasmic factors or enzymes
that are necessary for inactivation.