IMMUNOHISTOLOGICAL DEMONSTRATION OF CAV3.2 T-TYPE VOLTAGE-GATED CALCIUM CHANNEL EXPRESSION IN SOMA OF DORSAL ROOT GANGLION NEURONS AND PERIPHERAL AXONS OF RAT AND MOUSE

Previous behavioral studies have revealed that Ca(V)3.2 T-type calcium channels support peripheral nociceptive transmission and electrophysiological studies have established the presence of T-currents in putative nociceptive sensory neurons of dorsal root ganglion (DRG). To date, however, the localization pattern of this key nociceptive channel in the soma and peripheral axons of these cells has not been demonstrated due to lack of isoform-selective anti-Ca(V)3.2 antibodies. In the present study a new polyclonal Ca(V)3.2 antibody is used to localize Ca(V)3.2 expression in rodent DRG neurons using different staining techniques including confocal and electron microscopy (EM). Confocal microscopy of both acutely dissociated cells and short-term cultures demonstrated strong immunofluorescence of anti-Ca(V)3.2 antibody that was largely confined to smaller diameter DRG neurons where it co-localized with established immuno-markers of unmyelinated nociceptors, such as, CGRP, IB4 and peripherin. In contrast, a smaller proportion of these Ca(V)3.2-labeled DRG cells also co-expressed neuro-filament 200 (NF200), a marker of myelinated sensory neurons. In the rat sciatic nerve preparation, confocal microscopy demonstrated anti-Ca(V)3.2 immunofluorescence which was co-localized with both peripherin and NF200. Further, EM revealed immuno-gold labeling of Ca(V)3.2 preferentially in association with unmyelinated sensory fibers from mouse sciatic nerve. Finally, we demonstrated the expression of Ca(V)3.2 channels in peripheral nerve endings of mouse hindpaw skin as shown by co-localization with Mrgpd-GFP-positive fibers. The Ca(V)3.2 expression within the soma and peripheral axons of nociceptive sensory neurons further demonstrates the importance of this channel in peripheral pain transmission. (c) 2013 IBRO. Published by Elsevier Ltd. All rights reserved.