Han Jaehee, Truell Jeffrey, Gnatenco Carmen, Kim Donghee
Department of Physiology, Gyeongsang National University School of Medicine, Chinju, Korea.
J Physiol. 2002 Jul 15;542(Pt 2):431-44. doi: 10.1113/jphysiol.2002.017590.
Cerebellar granule neurons express a standing outward (background) K+ current (I(K,SO)) that regulates the resting membrane potential and cell excitability. As several tandem-pore (2P) K+ channel mRNAs are highly expressed in cerebellar granule cells, we studied whether, and which, 2P K+ channels contribute to I(K,SO). I(K,SO) was highly sensitive to changes in extracellular pH and was partially inhibited by acetylcholine, as reported previously. In cell-attached patches from cultured cerebellar granule neurons, four types of K+ channels were found to be active when membrane potential was held at -50 mV or +50 mV in symmetrical 140 mM KCl. Based on single-channel conductances, gating kinetics and modulation by pharmacological agents and pH, three K+ channels could be considered as functional correlates of TASK-1, TASK-3 and TREK-2, which are members of the 2P K+ channel family. The fourth K+ channel (Type 4) has not been described previously and its molecular correlate is not yet known. Based on the measurement of channel current densities, the Type 2 (TASK-3) and the Type 4 K+ channels were determined to be the major sources of I(K,SO) in cultured cerebellar granule neurons. The Type 1 (TASK-1) and Type 3 (TREK-2) activities were relatively low throughout cell growth in culture (1-10 days). Similar to TASK-1 and TASK-3, the Type 4 K+ channel was highly sensitive to changes in extracellular pH, showing a 78 % inhibition by changing the extracellular pH from 7.3 to 6.3. The results of this study show that three 2P K+ channels and an additional pH-sensing K+ channel (Type 4) comprise the I(K,SO) in cultured cerebellar granule neurons. Our results also show that the high sensitivity of I(K,SO) to extracellular pH comes from the high sensitivity of Type 2 (TASK-3) and Type 4 K+ channels.
小脑颗粒神经元表达一种外向性稳定(背景)钾电流(I(K,SO)),该电流调节静息膜电位和细胞兴奋性。由于几种串联孔道(2P)钾通道mRNA在小脑颗粒细胞中高度表达,我们研究了2P钾通道是否以及哪些通道对I(K,SO)有贡献。如先前报道,I(K,SO)对细胞外pH变化高度敏感,并部分受乙酰胆碱抑制。在培养的小脑颗粒神经元的细胞贴附式膜片中,当膜电位在对称的140 mM KCl中保持在 -50 mV或 +50 mV时,发现有四种类型的钾通道是活跃的。基于单通道电导、门控动力学以及药理试剂和pH的调节作用,三种钾通道可被视为TASK-1、TASK-3和TREK-2的功能对应物,它们是2P钾通道家族的成员。第四种钾通道(4型)此前未被描述,其分子对应物尚不清楚。基于通道电流密度的测量,确定2型(TASK-3)和4型钾通道是培养的小脑颗粒神经元中I(K,SO)的主要来源。在培养(1 - 10天)的整个细胞生长过程中,1型(TASK-1)和3型(TREK-2)的活性相对较低。与TASK-1和TASK-3类似,4型钾通道对细胞外pH变化高度敏感,将细胞外pH从7.3变为6.3时,抑制率达78%。本研究结果表明,三种2P钾通道和一种额外的pH敏感钾通道(4型)构成了培养的小脑颗粒神经元中的I(K,SO)。我们的结果还表明,I(K,SO)对细胞外pH的高敏感性源于2型(TASK-3)和4型钾通道的高敏感性。