RT Journal Article
SR Electronic
T1 Developmental Expression of the TTX-Resistant Voltage-Gated Sodium Channels Na<sub>v</sub>1.8 (SNS) and Na<sub>v</sub>1.9 (SNS2) in Primary Sensory Neurons
JF The Journal of Neuroscience
JO J. Neurosci.
FD Society for Neuroscience
SP 6077
OP 6085
DO 10.1523/JNEUROSCI.21-16-06077.2001
VO 21
IS 16
A1 Susanna C. Benn
A1 Michael Costigan
A1 Simon Tate
A1 Maria Fitzgerald
A1 Clifford J. Woolf
YR 2001
UL http://www.jneurosci.org/content/21/16/6077.abstract
AB The development of neuronal excitability involves the coordinated expression of different voltage-gated ion channels. We have characterized the expression of two sensory neuron-specific tetrodotoxin-resistant sodium channel α subunits, Nav1. (SNS/PN3) and Nav1.9 (SNS2/NaN), in developing rat lumbar dorsal root ganglia (DRGs). Expression of both Nav1.8 and Nav1.9 increases with age, beginning at embryonic day (E) 15 and E17, respectively, and reaching adult levels by postnatal day 7. Their distribution is restricted mainly to those subpopulations of primary sensory neurons in developing and adult DRGs that give rise to unmyelinated C-fibers (neurofilament 200 negative). Nav1.8 is expressed in a higher proportion of neuronal profiles than Nav1.9 at all stages during development, as in the adult. At E17, almost all Nav1.8-expressing neurons also express the high-affinity NGF receptor TrkA, and only a small proportion bind to IB4, a marker for c-ret-expressing (glial-derived neurotrophic factor-responsive) neurons. Because IB4 binding neurons differentiate from TrkA neurons in the postnatal period, the proportion of Nav1.8 cells that bind to IB4 increases, in parallel with a decrease in the proportion of Nav1.8–TrkA co-expressing cells. In contrast, an equal number of Nav1.9 cells bind IB4 and TrkA in embryonic life. The differential expression of Nav1.8 and Nav1.9 in late embryonic development, with their distinctive kinetic properties, may contribute to the development of spontaneous and stimulus-evoked excitability in small diameter primary sensory neurons in the perinatal period and the activity-dependent changes in differentiation they produce.