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酸敏感离子通道2(ASIC2)调节海马神经元中ASIC1的H⁺激活电流。

Acid-sensing ion channel 2 (ASIC2) modulates ASIC1 H+-activated currents in hippocampal neurons.

作者信息

Askwith Candice C, Wemmie John A, Price Margaret P, Rokhlina Tania, Welsh Michael J

机构信息

Department of Internal Medicine, Howard Hughes Medical Institute, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

J Biol Chem. 2004 Apr 30;279(18):18296-305. doi: 10.1074/jbc.M312145200. Epub 2004 Feb 11.

Abstract

Hippocampal neurons express subunits of the acid-sensing ion channel (ASIC1 and ASIC2) and exhibit large cation currents that are transiently activated by acidic extracellular solutions. Earlier work indicated that ASIC1 contributed to the current in these neurons and suggested its importance for normal behavior. However, the specific contribution of ASIC1 and ASIC2 subunits to acid-evoked currents in hippocampal neurons remained uncertain. To decipher the individual role of the ASIC subunits, we studied H(+)-gated currents in neurons from both ASIC1 and ASIC2 null mice. We found that much of the current was produced by ASIC1a/2a heteromultimeric channels, and individual subunits made distinct contributions. The ASIC1a subunit was key in establishing current amplitude. The ASIC2a subunit had little effect on amplitude but influenced desensitization, recovery from desensitization, pH sensitivity, and the response to modulatory agents. We also found heterogeneity in the contribution of ASIC2 throughout the neuronal population, with individual neurons expressing both ASIC1a homomultimeric and ASIC1a/2a heteromultimeric channels. Studies of neurons heterozygous for disrupted ASIC alleles indicated that the properties of H(+)-gated currents are dependent on the proportion of the individual subunits. These findings indicate that the absolute and relative amounts of ASIC subunits determine the amplitude and properties of hippocampal H(+)-gated currents and therefore may contribute to normal physiology and pathophysiology.

摘要

海马神经元表达酸敏感离子通道的亚基(ASIC1和ASIC2),并表现出大的阳离子电流,这些电流可被酸性细胞外溶液短暂激活。早期研究表明,ASIC1对这些神经元中的电流有贡献,并表明其对正常行为的重要性。然而,ASIC1和ASIC2亚基对海马神经元酸诱发电流的具体贡献仍不确定。为了解析ASIC亚基的个体作用,我们研究了来自ASIC1和ASIC2基因敲除小鼠神经元中的H⁺门控电流。我们发现,大部分电流是由ASIC1a/2a异源多聚体通道产生的,且各个亚基发挥了不同的作用。ASIC1a亚基是确定电流幅度的关键。ASIC2a亚基对幅度影响不大,但影响脱敏、脱敏恢复、pH敏感性以及对调节剂的反应。我们还发现,在整个神经元群体中,ASIC2的贡献存在异质性,单个神经元同时表达ASIC1a同源多聚体和ASIC1a/2a异源多聚体通道。对ASIC等位基因破坏的杂合神经元的研究表明,H⁺门控电流的特性取决于各个亚基的比例。这些发现表明,ASIC亚基的绝对和相对量决定了海马H⁺门控电流的幅度和特性,因此可能对正常生理和病理生理有影响。

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