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Kv1.3/Kv1.5异源通道损害巨噬细胞中的药理反应。

Kv1.3/Kv1.5 heteromeric channels compromise pharmacological responses in macrophages.

作者信息

Villalonga Núria, Escalada Artur, Vicente Rubén, Sánchez-Tilló Ester, Celada Antonio, Solsona Carles, Felipe Antonio

机构信息

Molecular Physiology Laboratory, Departament de Bioquímica i Biologia Molecular, Universitat de Barcelona, Avda. Diagonal 645, E-08028 Barcelona, Spain.

出版信息

Biochem Biophys Res Commun. 2007 Jan 26;352(4):913-8. doi: 10.1016/j.bbrc.2006.11.120. Epub 2006 Dec 4.

Abstract

Voltage-dependent K(+) (Kv) channels are involved in the immune response. Kv1.3 is highly expressed in activated macrophages and T-effector memory cells of autoimmune disease patients. Macrophages are actively involved in T-cell activation by cytokine production and antigen presentation. However, unlike T-cells, macrophages express Kv1.5, which is resistant to Kv1.3-drugs. We demonstrate that mononuclear phagocytes express different Kv1.3/Kv1.5 ratios, leading to biophysically and pharmacologically distinct channels. Therefore, Kv1.3-based treatments to alter physiological responses, such as proliferation and activation, are impaired by Kv1.5 expression. The presence of Kv1.5 in the macrophagic lineage should be taken into account when designing Kv1.3-based therapies.

摘要

电压依赖性钾离子(Kv)通道参与免疫反应。Kv1.3在自身免疫性疾病患者的活化巨噬细胞和效应记忆T细胞中高度表达。巨噬细胞通过细胞因子产生和抗原呈递积极参与T细胞活化。然而,与T细胞不同,巨噬细胞表达Kv1.5,其对Kv1.3药物具有抗性。我们证明单核吞噬细胞表达不同的Kv1.3/Kv1.5比率,导致在生物物理和药理学上不同的通道。因此,基于Kv1.3的改变生理反应(如增殖和活化)的治疗会因Kv1.5的表达而受损。在设计基于Kv1.3的疗法时,应考虑巨噬细胞谱系中Kv1.5的存在。

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