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大鼠背根神经节神经元中双孔域酸敏感钾通道表达的年龄相关性变化。

Age-related changes in two-pore domain acid-sensitive K⁺ channel expression in rat dorsal root ganglion neurons.

机构信息

Medical Research Centre for Neural Dysfunction, Department of Physiology and Institute of Health Sciences, Gyeongsang National University School of Medicine, Jinju, Korea.

出版信息

Clin Exp Pharmacol Physiol. 2012 Jan;39(1):43-8. doi: 10.1111/j.1440-1681.2011.05634.x.

Abstract
  1. Two-pore domain K⁺ (K(2P) ) channel expression influences brain development. The K(2P) 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 K(2P) 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 (∼10% in TASK-2 and ∼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.
摘要
  1. 双孔域钾离子(K(2P))通道表达影响大脑发育。K(2P)通道,包括双孔域酸敏感钾离子(TASK)通道,有助于神经元的静息膜电位的设定。除了大脑中的神经元外,背根神经节(DRG)神经元也表达 K(2P)通道。本研究的目的是鉴定 TASK 通道在 DRG 神经元中的表达在出生后的变化。

  2. 使用半定量聚合酶链反应、western blot 分析、免疫染色和膜片钳技术比较了新生(出生后第 1 天或第 2 天或 P2)和成年(P120)大鼠 DRG 中的 TASK 通道(TASK-1、TASK-2 和 TASK-3)的表达。

  3. 在成年(P120)大鼠 DRG 中,TASK-2 mRNA 和蛋白表达下调,而 TASK-3 mRNA 和蛋白表达上调。TASK-1 mRNA 和蛋白表达没有一致的变化。单通道记录显示,P1-P2 DRG 神经元中 TASK-2 和 TASK-3 样通道的表达非常低(TASK-2 约为 10%,TASK-3 约为 3%)。在 P120 DRG 中,TASK-2 样通道的检测减少,而 TASK-3 样通道的检测增加。

  4. 这些结果表明,TASK-2 和 TASK-3 mRNA 和蛋白表达在 DRG 神经元中发生年龄相关变化,表明 TASK-2 和 TASK-3 通道可能分别或共同参与 DRG 发育过程中新生儿和成年 DRG 神经元静息膜电位的设定。

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