The voltage-gated 'glial' sodium channel NaG belongs to a distinct molecula
r class within the multi-gene family of mammalian sodium channels. Original
ly found in central and peripheral glia, NaG has since been detected in neu
rons in rat dorsal root ganglia (DRG) and may play a role in Schwann cell-a
xon interactions. We have studied the presence of NaG-like immunoreactivity
in the intact and injured human peripheral nervous system using a specific
affinity-purified antibody. Nerve fibres in normal and injured peripheral
nerves and normal skin exhibited intense NaG-immunoreactivity. Numerous NaG
-immunoreactive nerve fibres surrounded neuronal cell bodies within postmor
tem control DRG, and in DRG avulsed from the spinal cord (i.e. after trauma
tic central axotomy). There were no significant differences in the pattern
of NaG immunostaining between control and avulsed DRG, or with delay after
injury. Generally, the neuronal cell bodies were only very weakly immunorea
ctive to NaG, indicating that the NaG immunoreactivity was predominantly in
Schwann cells/myelin. In accord, we demonstrated NaG immunostaining in cul
tured human and rat Schwann cells, and in distal nerve after wallerian dege
neration. NaG thus appears to be a useful new marker for Schwann cells in t
he human PNS, and a role in neuropathy deserves investigation.