Zhu Yaohui, Ye Jing, Huizinga Jan D
McMaster Univ., HSC-3N5C, 1200 Main St. West, Hamilton, ON L8N 3Z5, Canada.
Am J Physiol Gastrointest Liver Physiol. 2007 Jun;292(6):G1715-25. doi: 10.1152/ajpgi.00524.2006. Epub 2007 Mar 8.
Interstitial cells of Cajal (ICC) are pacemaker cells for gut peristaltic motor activity. Compared with cardiac pacemaker cells, little is known about mechanisms that regulate ICC excitability. The objective of the present study was to investigate a potential role for clotrimazole (CTL)-sensitive K currents (I(CTL)) in the regulation of ICC excitability and pacemaker activity. ICC were studied in situ and in short-term culture by using the whole cell patch-clamp configuration. In situ, ICC exhibited spontaneous transient inward currents followed by transient outward currents. CTL blocked outward currents, thereby increasing the net inward currents, and depolarized ICC, thereby establishing CTL-sensitive channels as regulators of ICC pacemaker activity. In short-term culture, a I(CTL) was identified that showed increased conductance when depolarized from the resting membrane potential to 0 mV and subsequent inward rectification at further depolarized potentials. The I(CTL) markedly increased with increasing intracellular calcium and was insensitive to the ether-à-go-go-related K channel blocker E-4031 and the large-conductance calcium-activated K channel blocker iberiotoxin. I(CTL) contributed 3-9 nS to the whole cell conductance at 0 mV membrane potential under physiological conditions; it was fast activating (tau = 88 ms), showed little time-dependent inactivation, and exhibited a deactivation time constant of 38 ms. The nitric oxide donor sodium nitroprusside (SNP) increased I(CTL). Single-channel activity, activated by calcium and SNP, was inhibited by CTL, with a single-channel conductance of approximately 38 pS. In summary, ICC generate a I(CTL) on depolarization through an intermediate-conductance calcium-activated K channel that regulates pacemaker activity and ICC excitability.
Cajal间质细胞(ICC)是肠道蠕动运动的起搏细胞。与心脏起搏细胞相比,关于调节ICC兴奋性的机制我们知之甚少。本研究的目的是探讨克霉唑(CTL)敏感钾电流(I(CTL))在调节ICC兴奋性和起搏活动中的潜在作用。通过使用全细胞膜片钳配置,对原位和短期培养的ICC进行了研究。在原位,ICC表现出自发性瞬时内向电流,随后是瞬时外向电流。CTL阻断外向电流,从而增加净内向电流,并使ICC去极化,从而将CTL敏感通道确立为ICC起搏活动的调节因子。在短期培养中,鉴定出一种I(CTL),当从静息膜电位去极化到0 mV时,其电导增加,在进一步去极化电位时出现内向整流。I(CTL)随着细胞内钙的增加而显著增加,并且对埃托啡相关钾通道阻滞剂E-4031和大电导钙激活钾通道阻滞剂iberiotoxin不敏感。在生理条件下,I(CTL)在0 mV膜电位时对全细胞电导的贡献为3-9 nS;它快速激活(时间常数tau = 88 ms),几乎没有时间依赖性失活,并且失活时间常数为38 ms。一氧化氮供体硝普钠(SNP)增加I(CTL)。由钙和SNP激活的单通道活性被CTL抑制,单通道电导约为38 pS。总之,ICC在去极化时通过中间电导钙激活钾通道产生I(CTL),该通道调节起搏活动和ICC兴奋性。