Journal of Neuroscience, Vol 9, 893-897, Copyright © 1989 by Society for Neuroscience
Expression of GAP-43, a rapidly transported growth-associated protein, and class II beta tubulin, a slowly transported cytoskeletal protein, are coordinated in regenerating neurons
PN Hoffman
Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
GAP-43 is a membrane-associated phosphoprotein enriched in elongating axons
(Meiri et al., 1986; Skene et al., 1986). After an axon has been
interrupted by cutting or crushing a nerve (axotomy), the portion of the
axon disconnected from the cell body (distal stump) degenerates and is
replaced by the outgrowth (elongation) of regenerating sprouts arising from
the proximal stump. Previous studies have shown that increased amounts of
pulse-labeled GAP-43 undergo fast axonal transport in regenerating neurons
(Benowitz et al., 1981; Skene and Willard, 1981 a, b). Using hybridization
with a cloned cDNA probe, I now show that mRNA levels for GAP-43 increase
in lumbar sensory neurons of rat after regeneration is initiated by
crushing the sciatic nerve; the relatively high levels of GAP-43 mRNA in
regenerating neurons are comparable to those in the developing neurons of
5-d-old animals. I further demonstrate that the induction of GAP-43
expression in regenerating neurons coincides temporally with an increase in
mRNA levels for class II beta tubulin (Hoffman and Cleveland, 1988),
suggesting that the expression of these proteins is closely coordinated
during axonal elongation.