Journal of Neuroscience, Vol 1, 1397-1406, Copyright © 1981 by Society for Neuroscience
Neuronal cell surfaces: distinctive glycoproteins of cultured adrenergic and cholinergic sympathetic neurons
SJ Braun, KJ Sweadner and PH Patterson
Cell surface components which are candidates for a role in nerve-target
interactions specific for neurons of particular transmitter types in the
sympathetic nervous system have been identified. Neurons of superior
cervical ganglia of neonatal rats were dissociated and cultured in the
virtual absence of non-neuronal cells under conditions previously found to
control their choice of neurotransmitter. When raised in medium conditioned
by heart cells, the neurons become cholinergic; when raised in medium which
depolarizes them, the neurons remain in their original adrenergic state.
The cell surface proteins of the neurons were labeled by either metabolic
or surface-specific methods, separated by two-dimensional polyacrylamide
gel electrophoresis, and visualized by autoradiography. A total of
approximately 35 glycoproteins can be resolved, of which at least 14 are
exposed on the cell surface. We evaluated glycoproteins of neurons raised
under conditions which differ in their potency for inducing cholinergic
properties: medium conditioned by skeletal muscle, liver, or heart cells or
medium containing 1 mM butyric acid. The expression of three neuronal
glycoproteins was correlated with the ability of a given culture condition
to induce the synthesis and accumulation of acetylcholine or
catecholamines. Two of these proteins are exposed on the cell surface, and
the third appears to be identical with a protein previously shown to be
secreted into the culture medium.