Slowing of neurofilament transport and the radial growth of developing nerve fibers

Several lines of evidence indicate that neurofilaments are major intrinsic determinants of axonal caliber in myelinated nerve fibers, and that the delivery of neurofilaments by slow axonal transport is an important mechanism by which neurons regulate axonal caliber. To further clarify the relationship between neurofilament transport and axonal caliber, we examined transport in developing motor fibers of rat sciatic nerve. In 3-, 10-, 12-, and 20-week-old rats, lumbar motor neurons were labeled by the intraspinal injection of radioactive amino acids, and the distributions of labeled cytoskeletal proteins within the sciatic nerve were analyzed at various times afterwards using sodium dodecyl sulfate-polyacrylamide gel electrophoresis, gel fluorography, and liquid scintillation spectroscopy. There was a progressive decline in the velocity of neurofilament transport with increasing distance along axons undergoing radial growth. By examining transport in different regions of the nerve in animals of the same age, we separated age-dependent reductions in velocity from those related to position along the nerve. The cross-sectional areas of these motor axons (in the L5 ventral root) increased linearly between 3 and 18 weeks of age. Quantitative electron microscopic analysis at 3 and 10 weeks of age revealed that neurofilament density was comparable in fibers of all calibers, indicating that the radial growth of these myelinated nerve fibers correlates with a proportional increase in neurofilament content. We propose that progressive reduction in the velocity of neurofilament transport along the nerve provides for radial growth during development.

[1]  J W Griffin,et al.  Changes in neurofilament transport coincide temporally with alterations in the caliber of axons in regenerating motor fibers , 1985, The Journal of cell biology.

[2]  J W Griffin,et al.  Control of axonal caliber by neurofilament transport , 1984, The Journal of cell biology.

[3]  D. Anthony,et al.  3,4-Dimethyl-2,5-hexanedione impairs the axonal transport of neurofilament proteins , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[4]  J. Stevens,et al.  Intracellular control of axial shape in non-uniform neurites: a serial electron microscopic analysis of organelles and microtubules in AI and AII retinal amacrine neurites , 1984, The Journal of cell biology.

[5]  D. Price,et al.  Neurotoxic probes of the axonal cytoskeleton , 1983, Trends in Neurosciences.

[6]  B. I. Roots Neurofilament accumulation induced in synapses by leupeptin. , 1983, Science.

[7]  D. Price,et al.  Slowing of the axonal transport of neurofilament proteins during development , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  D. Price,et al.  Microtubule-neurofilament segregation produced by beta, beta'- iminodipropionitrile: evidence for the association of fast axonal transport with microtubules , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  J. Julien,et al.  Multiple phosphorylation sites in mammalian neurofilament polypeptides. , 1982, The Journal of biological chemistry.

[10]  J. R. Morris,et al.  Stable polymers of the axonal cytoskeleton: the axoplasmic ghost , 1982, The Journal of cell biology.

[11]  R. Lasek,et al.  Axonal transport of the cytoskeleton in regenerating motor neurons: constancy and change , 1980, Brain Research.

[12]  Y. Komiya Slowing with age of the rate of slow axonal flow in bifurcating axons of rat dorsal root ganglion cells , 1980, Brain Research.

[13]  D. Price,et al.  Slow axonal transport of neurofilament proteins: impairment of beta,beta'-iminodipropionitrile administration. , 1978, Science.

[14]  R. Lasek,et al.  The slow component of axonal transport. Identification of major structural polypeptides of the axon and their generality among mammalian neurons , 1975, The Journal of cell biology.

[15]  A. Hendrickson,et al.  Changes in the rate of axoplasmic transport during postnatal development of the rabbit's optic nerve and tract. , 1971, Experimental neurology.

[16]  R. Friede,et al.  Axon caliber related to neurofilaments and microtubules in sciatic nerve fibers of rats and mice , 1970, The Anatomical record.

[17]  R. Lasek Axonal transport of proteins in dorsal root ganglion cells of the growing cat: A comparison of growing and mature neurons. , 1970, Brain research.

[18]  R. Friede,et al.  Analysis of the process of sheath expansion in swollen nerve fibers. , 1970, Brain research.

[19]  H. Wiśniewski,et al.  An ultrastructural study of experimental demyelination and remyelination. I. Acute experimental allergic encephalomyelitis in the peripheral nervous system. , 1969, Laboratory investigation; a journal of technical methods and pathology.

[20]  H. Wiśniewski,et al.  An ultrastructural study of experimental demyelination and remyelination. II. Chronic experimental allergic encephalomyelitis in the peripheral nervous system. , 1969, Laboratory investigation; a journal of technical methods and pathology.

[21]  J. E. Vaughn,et al.  MICROTUBULES AND FILAMENTS IN THE AXONS AND ASTROCYTES OF EARLY POSTNATAL RAT OPTIC NERVES , 1967, The Journal of cell biology.

[22]  B. Droz FATE OF NEWLY SYNTHESIZED PROTEINS IN NEURONS , 1965 .

[23]  J. Hursh CONDUCTION VELOCITY AND DIAMETER OF NERVE FIBERS , 1939 .