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Cited 6 time in webofscience Cited 6 time in scopus
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Age-related changes in two-pore domain acid-sensitive K plus channel expression in rat dorsal root ganglion neurons

Authors
Kim, Gyu-TaeCho, Young-WooTak, Hyun-MinLee, Jeong-SoonKim, Eun-JinHan, JaeheeKang, Dawon
Issue Date
Jan-2012
Publisher
WILEY
Keywords
ageing; dorsal root ganglia; potassium channel; two-pore domain acid-sensitive K plus (TASK) protein
Citation
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, v.39, no.1, pp.43 - 48
Indexed
SCIE
SCOPUS
Journal Title
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
Volume
39
Number
1
Start Page
43
End Page
48
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/22430
DOI
10.1111/j.1440-1681.2011.05634.x
ISSN
0305-1870
Abstract
1. Two-pore domain K+ (K2P) channel expression influences brain development. The K2P channels, including two-pore domain acid-sensitive K+ (TASK) channels, contribute to the setting of the resting membrane potential of neurons. In addition to neurons in the brain, dorsal root ganglion (DRG) neurons also express K2P channels. The aim of the present study was to identify postnatal changes in the expression of TASK channels in DRG neurons. 2. Expression of TASK channels (TASK-1, TASK-2 and TASK-3) was compared between neonatal (postnatal Day (P) 1 or P2) and adult (P120) rat DRG using semiquantitative polymerase chain reaction, western blot analysis, immunostaining and the patch-clamp technique. 3. In adult (P120) rat DRG, expression of TASK-2 mRNA and protein was downregulated, whereas TASK-3 mRNA and protein expression was upregulated. There were no consistent changes in TASK-1 mRNA and protein expression. Single-channel recordings showed very low TASK-2-and TASK-3-like channel expression in P1-P2 DRG neurons (similar to 10% in TASK-2 and similar to 3% in TASK-3). In P120 DRG, there was a reduction in the detection of TASK-2-like channels, whereas the detection of TASK-3-like channels increased. 4. These results show that TASK-2 and TASK-3 mRNA and protein expression undergoes age-related changes in DRG neurons, indicating that TASK-2 and TASK-3 channels are likely to contribute to the setting of the resting membrane potential of DRG neurons in neonates and adults, separately or together, during DRG development.
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