NaG, a member of subfamily 2, was originally characterized as a ''glia
l'' sodium channel, and is expressed at high levels in Schwann cells i
n vivo. However, NaG has also been shown by in situ hybridization to b
e highly expressed in rat dorsal root ganglion (DRG) neurons, which, l
ike Schwann cells, are neural crest derivatives. In the present study,
we used non-isotopic in situ hybridization with a riboprobe for NaG,
in conjunction with RT-PCR, to determine whether NaG is expressed in t
issues related to the DRG either by neural crest origin or sensory fun
ction. We found that the expression of significant levels of NaG mRNA
was restricted to derivatives of the neural crest (neurons of DRG, tri
geminal ganglion and mesencephalic nucleus of the trigeminal nerve, an
d Schwann and satellite cells); the absence of NaG from superior cervi
cal ganglion neurons and adrenal medulla chromaffin cells indicates th
at not all neural crest derived neural elements express NaG. NaG was n
ot observed in sensory neurons (retina, vestibular ganglion, spiral ga
nglion, olfactory epithelium) that are not of neural crest origin. Our
results indicate that NaG mRNA is expressed not only in Schwann cells
, but also in a spectrum of neuronal cell types with afferent function
of neural crest origin. NaG thus appears to represent a transcript en
coding a sodium channel or sodium channel-like protein that is uniquel
y expressed by both Schwann cells and afferent neurons of neural crest
origin. (C) 1997 Wiley-Liss, Inc.