K. Grant et al., PROJECTION NEURONS OF THE MORMYRID ELECTROSENSORY LATERAL-LINE LOBE -MORPHOLOGY IMMUNOHISTOCHEMISTRY, AND SYNAPTOLOGY, Journal of comparative neurology, 375(1), 1996, pp. 18-42
This paper describes the morphological, immunohistochemical, and synap
tic properties of projection neurons in the highly laminated medial an
d dorsolateral zones of the mormyrid electrosensory lateral line lobe
(ELL), These structures are involved in active electrolocation, i.e.,
the detection and localization of objects in the nearby environment of
the fish on the basis of changes in the reafferent electrosensory sig
nal generated by the animal's own electric organ discharge. Electrosen
sory, corollary electromotor command-associated signals (corollary dis
charges), and a variety of other inputs are integrated within the ELL
microcircuit. The organization of ELL projection neurons is analyzed a
t the light and electron microscopic levels based on Golgi impregnatio
ns, intracellular labeling, neuroanatomical tracer techniques, and gam
ma-aminobutyric acid (GABA), gamma-aminobutyric acid decarboxylase (GA
D), and glutamate immunohistochemistry. Two main types of ELL projecti
on neurons have been distinguished in mormyrids: large ganglionic (LG)
and large fusiform (LF) cells. LG cells have a multipolar cell body (
average diameter 13 mu m) in the ganglionic layer, whereas LF cells ha
ve a fusiform cell body (on average, about 10 x 20 mu m) in the granul
ar layer. Apart from the location and shape of their soma, the morphol
ogical properties of these cell types are largely similar. They are gl
utamatergic and project to the midbrain torus semicircularis, where th
eir axon terminals make axodendritic synaptic contacts in the lateral
nucleus. They have 6-12 apical dendrites in the molecular layer, with
about 10,000 spines contacted by GABA-negative terminals and about 3,0
00 GABA-positive contacts on the smooth dendritic surface between the
spines. Their somata and short, smooth basal dendrites, which arborize
in the plexiform layer (LG cells) or in the granular layer (LF cells)
, are densely covered with GABA-positive, inhibitory terminals. Correl
ation with physiological data suggests that LG cells are I units, whic
h are inhibited by stimulation of the center of their receptive fields
, and LF cells are E units, excited by electric stimulation of the rec
eptive field center. Comparison with the projection neurons of the ELL
of gymnotiform fish, which constitute another group of active electro
locating teleosts, shows some striking differences, emphasizing the in
dependent development of the ELL in both groups of teleosts. (C) 1996
Wiley-Liss, Inc.