Korean J Physiol Pharmacol.  2008 Oct;12(5):245-251. 10.4196/kjpp.2008.12.5.245.

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 Neurons

• Jang I
• La JH
• Kim GT
• Lee JS
• Kim EJ
• Lee ES
• Kim SJ
• Seo JM
• Ahn SH
• Park JY
• Hong SG
• Kang D
• Han J

• KMID: 1486106
• DOI: http://doi.org/10.4196/kjpp.2008.12.5.245

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.

Keyword

Two-pore domain K+ channel; Dorsal root ganglion; Spinal cord injuries; Acidosis

MeSH Terms

Acidosis
Animals
Brain
Clone Cells
Diagnosis-Related Groups
Ganglia, Spinal
Humans
Hydrogen-Ion Concentration
Kinetics
Neurons
Rats
RNA, Messenger
Spinal Cord
Spinal Cord Injuries
Spinal Nerve Roots
Up-Regulation
RNA, Messenger

Figure

• 

  Fig. 1. pH sensitive background K+ channels in DRG neurons. (A) Photomicrograph of DRG neurons cultured for two days in medium containing NGF. These neurons were isolated from postnatal day 1 or 2 (P1-2) rats. Scale bar, 50 μm. (B) The expression of K2P channel mRNA. In the P1~2 rat DRG, PCR products of TASK-1 (702 bp), TASK-2 (441 bp), TASK-3 (517 bp), TREK-1 (361 bp), TREK-2 (493 bp), TRAAK (445 bp), and TRESK (475 bp) were obtained and confirmed by sequencing. (C) Cell-attached patches were formed on DRG neurons, and single-channel openings were recorded at +60 mV and −60 mV at room temperature. Pipette and bath solutions contained 150 mM KCl. Representative traces show five types of single-channel current at +60 mV (upper trace), 0 mV (middle), and −60 mV (lower). The horizontal scale bar indicates 100 ms. The vertical scale bar indicates 2 pA for TRESK and 6 pA for other channels. Bar graphs show the pH sensitivity of each channel (mean±SE, n=4~6). ∗p<0.05 and ∗∗p<0.01 compared to the corresponding control (pH 7.3).

• 

  Fig. 2. Single-channel kinetics of TASK-3-like K+ channels in DRG neurons. (A) Cell-attached patches were formed, and single-channel openings were recorded at the different membrane potentials, noted on the left. Pipette and bath solutions contained 150 mM KCl. (B) Histograms of open time duration (left) and amplitude (right) of TASK-3-like K+ channel were obtained from openings at −60 mV. They were fitted by single exponential and Gaussian functions, respectively. (C) Single-channel amplitudes were determined from the amplitude histogram for each membrane potential in order to construct the current-voltage relationship. Each point represents mean±SD of four repeated experiments. (D) The pHo sensitivity of single-channel currents from TASK-3-like K+ channels in DRG neurons. Single-channel currents from outside-out patches are shown as inward currents recorded at −60 mV when KCl concentration was 150 mM on both sides of the patch. Typical channel openings from three independent experiments are shown. The bar graph shows the effects of pHo changes on TASK-3-like K+ channel activity. Each bar represents mean±SD of three repeated experiments. The asterisk indicates significant difference from the control value at pH 7.3 (p<0.05).

• 

  Fig. 3. Up-regulation of TASK-3 mRNA and protein expression after spinal cord injury. (A) A photograph of rats with a T9 spinal segment injury. These rats exhibited paralysis of the hind legs. (B) The BBB open-field locomotor rating scores show spontaneous partial recovery of motor function after SCI (n=10 animals per group). Data points represent mean±SD. (C) Changes in TASK-3 mRNA expression in SCI animals. PCR was conducted on cDNA templates obtained from brain, spinal cord, and DRG of SCI and sham-operated animals at 48 hours after injury. The bar graph summarizes the levels of TASK-3 mRNA expression which changed after SCI. Each bar represents mean±SD of three repeated experiments. Asterisks indicate significant difference from the corresponding control value (sham-operated groups, p <0.05). (D) Western blot analysis in DRG. TASK-3 protein level increased in DRG obtained from SCI animal at 48 hours after injury. The bar graph shows the up-regulation of TASK-3 protein expression in DRG obtained from SCI animals. Each bar represents mean±SD of three repeated experiments. Asterisks (∗∗) indicate significant difference from the corresponding control value (sham-operated groups, p<0.01).

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