Single-Channel Recording of TASK-3-like K+ Channel and Up-Regulation of TASK-3 mRNA Expression after Spinal Cord Injury in Rat Dorsal Root Ganglion Neuronsopen access
- Authors
- Jang, Inseok; La, Jun-Ho; Kim, Gyu-Tae; Lee, Jeong-Soon; Kim, Eun-Jin; Lee, Eun-Shin; Kim, Su-Jeong; Seo, Jeong-Min; Ahn, Sang-Ho; Park, Jae-Yong; Hong, Seong-Geun; Kang, Dawon; Han, Jaehee
- Issue Date
- Oct-2008
- Publisher
- KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY
- Keywords
- Two-pore domain K+ channel; Dorsal root ganglion; Spinal cord injuries; Acidosis
- Citation
- KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.12, no.5, pp 245 - 251
- Pages
- 7
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY
- Volume
- 12
- Number
- 5
- Start Page
- 245
- End Page
- 251
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/27254
- DOI
- 10.4196/kjpp.2008.12.5.245
- ISSN
- 1226-4512
2093-3827
- Abstract
- Single-channel recordings of TASK-1 and TASK-3, members of two-pore domain K+ channel family, have not yet been reported in dorsal root ganglion (DRG) neurons, even though their mRNA and activity in whole-cell currents have been detected in these neurons. Here, we report single-channel kinetics of the TASK-3-like K+ channel in DRG neurons and up-regulation of TASK-3 mRNA expression in tissues isolated from animals with spinal cord injury (SCI). In DRG neurons, the single-channel conductance of TASK-3-like K+ channel was 33.0 +/- 0.1 pS at -60 mV, and TASK-3 activity fell by 65 +/- 5% when the extracellular pH was changed from 7.3 to 6.3, indicating that the DRG K+ channel is similar to cloned TASK-3 channel. TASK-3 mRNA and protein levels in brain, spinal cord, and DRG were significantly higher in injured animals than in sham-operated ones. These results indicate that TASK-3 channels are expressed and functional in DRG neurons and the expression level is up-regulated following SCI, and suggest that TASK-3 channel could act as a potential background K+ channel under SCI-induced acidic condition.
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