Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1984 Jan;98(1):364-8.
doi: 10.1083/jcb.98.1.364.

A few axonal proteins distinguish ventral spinal cord neurons from dorsal root ganglion neurons

A few axonal proteins distinguish ventral spinal cord neurons from dorsal root ganglion neurons

P Sonderegger et al. J Cell Biol. 1984 Jan.

Abstract

A series of proteins putatively involved in the generation of axonal diversity was identified. Neurons from ventral spinal cord and dorsal root ganglia were grown in a compartmented cell-culture system which offers separate access to cell somas and axons. The proteins synthesized in the neuronal cell somas and subsequently transported into the axons were selectively analyzed by 2-dimensional gel electrophoresis. The patterns of axonal proteins were substantially less complex than those derived from the proteins of neuronal cell bodies. The structural and functional similarity of axons from different neurons was reflected in a high degree of similarity of the gel pattern of the axonal proteins from sensory ganglia and spinal cord neurons. Each axonal type, however, had several proteins that were markedly less abundant or absent in the other. These neuron-population enriched proteins may be involved in the implementation of neuronal diversity. One of the proteins enriched in dorsal root ganglia axons had previously been found to be expressed with decreased abundance when dorsal root ganglia axons were co-cultured with ventral spinal cord cells under conditions in which synapse formation occurs (P. Sonderegger, M. C. Fishman, M. Bokoum, H. C. Bauer, and P.G. Nelson, 1983, Science [Wash. DC], 221:1294-1297). This protein may be a candidate for a role in growth cone functions, specific for neuronal subsets, such as pathfinding and selective axon fasciculation or the initiation of specific synapses. The methodology presented is thus capable of demonstrating patterns of protein synthesis that distinguish different neuronal subsets. The accessibility of these proteins for structural and functional studies may contribute to the elucidation of neuron-specific functions at the molecular level.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Neurochem. 1969 Jan;16(1):67-81 - PubMed
    1. J Biol Chem. 1972 May 25;247(10):3159-69 - PubMed
    1. Dev Biol. 1972 Jun;28(2):407-29 - PubMed
    1. Z Zellforsch Mikrosk Anat. 1973;138(4):475-88 - PubMed
    1. Dev Biol. 1974 Mar;37(1):100-16 - PubMed

Publication types

Substances