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. 2013 Dec;11(6):621–640. doi: 10.2174/1570159X113119990042

Table 1.

K+ Channel Expression in Peripheral Somatosensory System

K+ Channel Family a-subunit Species Assay Commentary Ref.
Kv1 Kv1.1 - 1.6 Rat RNase protection assay, RT-PCR Kv1.1 and Kv1.2 mRNAs were highly abundant while Kv1.3 - 1.6 mRNAs were detected at lower levels in L4-L5 DRGs [28, 32]
Kv1.1, Kv1.2, Kv1.4 Rat IHC, electrophys. Kv1.1 and Kv1.2 were predominantly found in large DRG neurons; small-diameter DRG neurons predominantly (but not exclusively) expressed Kv1.4. IB4-positive neurons expressed mostly Kv1.4 [31, 33]
Kv2 Kv2.1, Kv2.2 Rat RT-PCR, IHC, electrophys. mRNA products were found in the whole ganglion lysates and immunoreactivity found in cultured small neurons [32, 35]
Kv2.1, Kv2.2 Rat IHC, in situ hybridization Kv2.1 and Kv2.2 immunoreactivity and mRNA products were detected in DRG neurons of all sizes [36]
Kv3 Kv3.1, Kv3.2, Kv3.5 Rat RT-PCR mRNA products were found in the whole ganglion lysates [32]
Kv3.4 Rat IHC Kv3.4 expression was found mainly in C fibres (including axons, cell bodies and central terminals) [38]
Kv4 Kv4.1, Kv4.2, Kv4.3 Rat RT-PCR mRNA products were found in the whole ganglion lysates [32]
Kv4.1, Kv4.3 Rat RT-PCR, IHC, electrophys. mRNA and immunoreactivity of Kv4.1 and 4.3 (but not Kv4.2) was detected in small DRG neurons [39]
Kv4.1, Kv4.3 Rat In situ hybridization, IHC mRNA products and immunoreactivity of Kv4.1 and 4.3 (but not Kv4.2) were detected. Kv4.3 was found mostly in small neurons while Kv4.1 in neurons of all sizes [40]
Kv4.3 Rat IHC Kv4.3 expression was found mainly in non-peptidergic nociceptors [38]
Kv7 Kv7.2, Kv7.3, Kv7.5 Rat RT-PCR, IHC,
Electrophys.
Detection of mRNA and immunoreactivity of Kv7.2, Kv7.3 and Kv7.5 in cultured DRG neurons of all sizes. M-like currents were recorded from small DRG neurons [44]
Kv7.2 Rat RT-PCR, IHC, electrophys. Kv7.2 was found to be predominantly expressed in small nociceptive neurons and unmyelinated fibres. M-like currents were recorded from acute DRG slices from adult rats [45]
Kv7.2 Rat IHC, electrophys. Kv7.2 immunoreactivity was reported in skin terminals and afferents of Ad and C fibres. M current activity in the fibres was confirmed electrophysiologically [48]
Kv7.2 Rat IHC Kv7.2 immunoreactivity was enriched in the nodes of Ranvier of myelinated fibres [49, 50]
Kv7.2, Kv7.3, Kv7.5 Rat, mouse IHC Kv7.2 was found predominantly expressed in large DRG neurons and in the nodes of Ranvier of myelinated fibres; Kv7.3 was found in the nodes as well. Kv7.5 immunoreactivity was found predominantly in small neurons [46]
Kv7.2, Kv7.3, Kv7.5 Rat IHC, electrophys. Expression of Kv7.2, Kv7.3 and Kv7.5 was found in the peripheral terminals of the aortic depressor nerve (nodose ganglion neurons). Kv7.2 was found in un-myelinated C fibres [57]
Silent Kvs Kv8.1, Kv9.1, Kv9.3 Rat RT-PCR, IHC, electrophys. mRNA products were found in the whole ganglion lysates and immunoreactivity for Kv9.1 and 9.3 was found in cultured small neurons [35]
Kv9.1 Rat IHC, in situ hybridization Kv9.1 immunoreactivity was detected in predominantly large, myelinated DRG neurons [36]
K2P TASK-1, TASK-3, TREK-1, TRAAK, TWIK-1 Rat In situ hybridization mRNA products were found in various subpopulations of DRG neurons. TWIK-1 was more abundant in large neurons [63]
K2P TRESK, TRAAK, TREK-2, TWIK-2, TREK-1, THIK-2, TASK-1, TASK-2, THIK-1, TASK-3 Rat RT-PCR Whole DRG lysates were analysed for K2P expression, the mRNA abundances were found to follow the order of TRESK > TRAAK > TREK-2 = TWIK-2 > TREK-1=THIK-2 >TASK-1>TASK-2 > THIK-1 = TASK-3 [64]
TREK-2, TRESK,
TREK-1,
TREK-2, TRAAK
Rat Correlative single-channel analysis, RT-PCR TREK-2 and TRESK were found to underlie the majority of background K+ conductance in small- and medium-size DRG in culture [65]
TREK-1 Mouse IHC TREK-1 immunoreactivity was abundant in DRG sections, small- and medium-sized neurons were stained predominantly [68]
TASK-1, TASK-2, TASK-3 Rat IHC Expression of three TASK subunits in subpopulations of small- and medium-diameter DRG neurons have been characterized [160]
KATP Kir6.1, Kir6.2, SUR1, SUR2 Rat RT-PCR, IHC, western blot Kir6.1, Kir6.2, SUR1 and SUR2 mRNA products were found in whole DRG lysates; protein expression for all but Kir6.1 was confirmed by western blot and immunohistochemistry in subpopulation of neurons of various sizes [74]
Slo Slo1, rb2 Rat RT-PCR, electrophys. Presence of Slo1/rb2 channels in small-diameter DRG neurons has been verified by correlative patch clamp analysis; rb2 expression was confirmed by RT-PCR from whole ganglion lysates [78]
Slo2.1, Slo2.2 Rat RT-PCR, electrophys. KNa currents were recorded in medium-size DRG neurons, presence of Slo2.1, Slo2.2 mRNA was confirmed by RT-PCR from whole ganglion lysates [81]
Slo2.2 Rat IHC, electrophys. Slo2.2 immunoreactivity and KNa currents were found in DRG neurons of all sizes (≈90% of all neurons) [80]

IHC, immunohistochemistry.