Effects of electrical activity on GAP-43 expression were tested in mou
se dorsal root ganglion (DRG) neurons subjected to electrical stimulat
ion in culture. Patterned electrical stimulation was provided through
extracellular electrodes placed in multicompartment cell culture chamb
ers. Stimulation was delivered at 10 Hz, in 0.5 s bursts every 2 s for
up to 3 days. Expression of GAP-43 was assessed by immunocytochemistr
y, two ELISA methods, and Northern blot analysis within three experime
ntal protocols: (1) prior to synaptogenesis, (2) after synaptogenesis
with spinal cord neurons, and (3) within the context of activity-depen
dent synaptic competition, in which synapses from active and inactive
DRG neurons converge on the same postsynaptic neurons. None of the sti
mulation treatments produced a measurable change in GAP-43 or RNA mess
age for the protein, although this electrical stimulus induces persist
ent changes in synaptic strength, and alters neurite outgrowth in thes
e cultures. The decline in GAP-43 levels between 1 and 3 weeks in cult
ure, which has been reported in other studies, was readily detectable
by our measurements. We conclude that regulation of GAP-43 expression
is not required for activity-dependent regulation of growth cone motil
ity, synaptogenesis and synapse elimination, or changes in synaptic st
rength. Instead, post-translational modification, such as phosphorylat
ion, may be the primary means of regulating any GAP-43 functions assoc
iated with these activity-dependent processes.