Journal of Neuroscience, Vol 8, 1656-1670, Copyright © 1988 by Society for Neuroscience
Electrotonic synapses between Aplysia neurons in situ and in culture: aspects of regulation and measurements of permeability
R Bodmer, V Verselis, IB Levitan and DC Spray
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461.
Properties of electrotonic synapses between L14 neurons in the abdominal
ganglion of the marine mollusc Aplysia californica were examined in situ
and between unidentified buccal neurons maintained in tissue culture. In
culture, depolarizing postsynaptic potentials in response to a train of
action potentials showed apparent facilitation with increasing spike
number, which was attributable to the low-pass filter properties of
electrotonic transmission via gap junctions and to network properties. Gap
junctional conductance (gj), calculated from current-clamp data or measured
directly under voltage clamp, indicated no significant dependence of gj on
transjunctional or inside-outside potential in situ or in culture. Octanol,
a local anesthetic agent that reduces gj in many other systems, had no
effect on gj between Aplysia neurons. The effect of intracellular
acidification, a treatment that rapidly and reversibly uncouples a variety
of cell types, reduced gj between Aplysia neurons but did not completely
abolish it. The relationship between intracellular pH (pHi), measured with
ion- sensitive microelectrodes, and gj was steeper in cultured neurons than
in situ and was maximally reduced by 70-80%, as compared to 50% or less in
situ at the lowest pHi values tested. The coupling coefficient (k) was
reduced less by low pHi than was gj, which could be explained by a
simultaneous increase in nonjunctional membrane resistance. Permeability
properties of Aplysia electrotonic synapses to a variety of tracer
molecules were also examined between identified L 14 neurons in situ and in
dissociated buccal, abdominal, and bag neurons in culture. The fluorescent
dyes Lucifer yellow, 6-carboxyfluorescein, and dichlorofluorescein (1.2-1.4
nm maximal diameters) did not spread detectably from an injected neuron to
its electrically coupled neighbors, regardless of the strength of
electrotonic coupling. However, the smaller tetraalkylammonium ions TMA and
TEA (diameters 0.66 and 0.8 nm, concentrations measured with ion-selective
electrodes), could be detected in neighboring cells within minutes. In
culture, transfer of the tetraalkylammonium ions was slow and not easily
detectable in cell pairs where gj was low (less than 20 nS). The
permeability was as high as 10(-10) cm3/sec in situ and 10(-12) cm3/sec in
culture, and values were roughly correlated with simultaneously measured
values of gj. Electrotonic synapses in the nervous system of Aplysia,
therefore, have a quantitatively different spectrum of sensitivities than
has been found for gap junctions of other systems and appear to possess
reduced permeability to tracer molecules.