Zhu Yaohui, Golden Catherine M, Ye Jing, Wang Xuan-Yu, Akbarali Hamid I, Huizinga Jan D
Intestinal Disease Research Program, McMaster University, Hamilton, Ontario, Canada L8N 3Z5.
Am J Physiol Gastrointest Liver Physiol. 2003 Dec;285(6):G1249-58. doi: 10.1152/ajpgi.00149.2003. Epub 2003 Sep 4.
Ether-à-go-go-related gene (ERG) K channels have been implicated in the generation of pacemaker activities in the heart. To study the presence and function of ERG K channels in the pacemaker cells of the small intestine [the interstitial cells of Cajal (ICC)], a combination of patch-clamp techniques, tissue and live cell immunohistochemistry, RT-PCR, and in vitro functional studies were performed. Nonenzymatically isolated ICC in culture were identified by vital staining and presence of rhythmic inward currents. RT-PCR showed the presence of ERG mRNA in the intestinal musculature, and immunohistochemistry on tissue and cultured cells demonstrated that protein similar to human ERG was concentrated on ICC in the Auerbach's plexus region. Whole cell ERG K+ currents were evoked on hyperpolarization from 0 mV (but not from -70 mV) up to -120 mV and showed strong inward rectification. The currents were inhibited by E-4031, cisapride, La3+, and Gd3+ but not by 50 microM Ba2+. The ERG K+ inward current had a typical transient component with fast activation and inactivation kinetics followed by significant steady-state current. E-4031 also inhibited tetraethylammonium (TEA)-insensitive outward current indicating that the ERG K+ current is operating at depolarizing potentials. In contrast to TEA, blockers of the ERG K+ currents caused marked increase in tissue excitability as reflected by an increase in slow-wave duration and an increase in superimposed action potential activity. In summary, ERG K channels in ICC contribute to the membrane potential and play a role in regulation of pacemaker activity of the small intestine.
醚 - 去极化相关基因(ERG)钾通道与心脏起搏活动的产生有关。为了研究ERG钾通道在小肠起搏细胞(即 Cajal 间质细胞,ICC)中的存在及功能,我们进行了膜片钳技术、组织和活细胞免疫组织化学、逆转录聚合酶链反应(RT-PCR)以及体外功能研究的联合实验。通过活体染色和节律性内向电流的存在来鉴定培养中未经酶处理分离的 ICC。RT-PCR 显示肠道肌肉组织中存在 ERG 信使核糖核酸(mRNA),对组织和培养细胞进行的免疫组织化学表明,与人 ERG 相似的蛋白质集中在奥尔巴赫神经丛区域的 ICC 上。从 0 毫伏(而非 -70 毫伏)超极化至 -120 毫伏时可诱发全细胞 ERG 钾电流,且该电流表现出强烈的内向整流。该电流受到 E-4031、西沙必利、镧离子(La3 +)和钆离子(Gd3 +)的抑制,但不受 50 微摩尔钡离子(Ba2 +)的抑制。ERG 钾内向电流具有典型的瞬态成分,其激活和失活动力学较快,随后是显著的稳态电流。E-4031 还抑制了对四乙铵(TEA)不敏感的外向电流,表明 ERG 钾电流在去极化电位下起作用。与 TEA 不同,ERG 钾电流阻滞剂导致组织兴奋性显著增加,表现为慢波持续时间增加和叠加动作电位活动增加。总之,ICC 中的 ERG 钾通道有助于膜电位的形成,并在小肠起搏活动的调节中发挥作用。