Zhang Ping, Canessa Cecilia M
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
J Gen Physiol. 2002 Oct;120(4):553-66. doi: 10.1085/jgp.20028574.
The mammalian nervous system expresses proton-gated ion channels known as acid-sensing ion channels (ASICs). Depending on their location and specialization some neurons express more than one type of ASIC where they may form homo- or heteromeric channels. Macroscopic characteristics of the ASIC currents have been described, but little is known at the single channel level. Here, we have examined the properties of unitary currents of homomeric rat ASIC1alpha, ASIC2a, and ASIC3 expressed in Xenopus oocytes with the patch clamp technique. We describe and characterize properties unique to each of these channels that can be used to distinguish the various types of ASIC channels expressed in mammalian neurons. The amplitudes of the unitary currents in symmetrical Na(+) are similar for the three types of channels (23-18 pS) and are not voltage dependent. However, ASIC1alpha exhibits three subconductance states, ASIC2a exhibits only one, and ASIC3 none. The kinetics of the three types of channels are different: ASIC1alpha and ASIC2a shift between modes of activity, each mode has different open probability and kinetics. In contrast, the kinetics of ASIC3 are uniform throughout the burst of activity. ASIC1alpha, ASIC2a, and ASIC3 are activated by external protons with apparent pH(50) of 5.9, 5.0, and 5.4, respectively. Desensitization in the continual presence of protons is fast and complete in ASIC1alpha and ASIC3 (2.0 and 4.5 s(-1), respectively) but slow and only partial in ASIC2a (0.045 s(-1)). The response to external Ca(2+) also differs: micro M concentrations of extracellular Ca(2+) are necessary for proton gating of ASIC3 (EC(50) = 0.28 micro M), whereas ASIC1alpha and ASIC2a do not require Ca(2+). In addition, Ca(2+) inhibits ASIC1alpha (K(D) = 9.2 +/- 2 mM) by several mechanisms: decrease in the amplitude of unitary currents, shortening of the burst of activity, and decrease in the number of activated channels. Contrary to previous reports, our results indicate that the Ca(2+) permeability of ASIC1alpha is very small.
哺乳动物的神经系统表达一种被称为酸敏感离子通道(ASICs)的质子门控离子通道。根据其位置和特异性,一些神经元表达不止一种类型的ASIC,它们可能形成同聚体或异聚体通道。ASIC电流的宏观特征已有描述,但在单通道水平上了解甚少。在此,我们利用膜片钳技术研究了非洲爪蟾卵母细胞中表达的同聚体大鼠ASIC1α、ASIC2a和ASIC3的单通道电流特性。我们描述并表征了这些通道各自独特的特性,这些特性可用于区分哺乳动物神经元中表达的各种类型的ASIC通道。在对称的Na⁺中,这三种类型通道的单通道电流幅度相似(23 - 18 pS),且不依赖电压。然而,ASIC1α呈现三种亚电导状态,ASIC2a仅呈现一种,ASIC3则没有。这三种类型通道的动力学不同:ASIC1α和ASIC2a在不同活动模式之间转换,每种模式具有不同的开放概率和动力学。相比之下,ASIC3在整个活动爆发期间的动力学是一致的。ASIC1α、ASIC2a和ASIC3分别被细胞外质子激活,其表观pH(50)分别为5.9、5.0和5.4。在持续存在质子的情况下,ASIC1α和ASIC3的脱敏快速且完全(分别为2.0和4.5 s⁻¹),而ASIC2a的脱敏缓慢且仅部分发生(0.045 s⁻¹)。对细胞外Ca²⁺的反应也有所不同:微摩尔浓度的细胞外Ca²⁺对于ASIC3的质子门控是必需的(EC(50) = 0.28 μM),而ASIC1α和ASIC2a则不需要Ca²⁺。此外,Ca²⁺通过多种机制抑制ASIC1α(K(D) = 9.2 ± 2 mM):单通道电流幅度降低、活动爆发缩短以及激活通道数量减少。与先前的报道相反,我们的结果表明ASIC1α的Ca²⁺通透性非常小。