Journal of Neuroscience, Vol 7, 2256-2263, Copyright © 1987 by Society for Neuroscience
Effect of changes in neurofilament content on caliber of small axons: the beta,beta'-iminodipropionitrile model
IM Parhad, AW Clark and JW Griffin
The structural role of neurofilaments in the normal axon and the
consequences of altered axonal transport of neurofilaments have been
extensively studied in large axons. These studies suggest that
neurofilament numbers and interneurofilament spacing are major determinants
of axonal cross-sectional area. In contrast, in small axons and dendrites,
microtubules and membranous organelles appear to be the most closely
correlated with size and shape of the cell process. In this study we have
examined the effect of impairment in neurofilament transport on small
axons, typical of most CNS pathways. Neurofilament transport was impaired
by administration of beta,beta'- iminodipropionitrile (IDPN), resulting in
proximal accumulation and distal depletion of neurofilaments. The evolution
of these changes was studied in the optic nerves of guinea pigs treated
with IDPN, 1-35 weeks following intoxication. The effect of this
redistribution of neurofilaments on cross-sectional area of small axons was
evaluated using quantitative ultrastructural methods. Our results show that
with the alteration in neurofilament transport seen with IDPN intoxication,
there is a wide spectrum of neurofilament densities, ranging from a 5- fold
increase above normal in the proximal axon, to a 5-fold decrease below
normal in the distal axon. Although the optic nerve fibers enlarge with the
increase in neurofilament content, they do not atrophy significantly with
the continued loss of neurofilaments. We conclude that factors other than
neurofilament content are capable of maintaining size and shape of these
small axons. Candidate organelles include microtubules and membranous
organelles and possibly other axonal elements.