Markakis Ioannis, Charitakis Ioannis, Beeton Christine, Galani Melpomeni, Repousi Elpida, Aggeloglou Stella, Sfikakis Petros P, Pennington Michael W, Chandy K George, Poulopoulou Cornelia
National and Kapodistrian University of Athens, Medical School, Athens, Greece.
Department of Neurology, "St. Panteleimon" General State Hospital, Nikaia, Greece.
Front Pharmacol. 2021 Sep 23;12:714841. doi: 10.3389/fphar.2021.714841. eCollection 2021.
Voltage-gated Kv1.3 potassium channels are key regulators of T lymphocyte activation, proliferation and cytokine production, by providing the necessary membrane hyper-polarization for calcium influx following immune stimulation. It is noteworthy that an accumulating body of and evidence links these channels to multiple sclerosis pathophysiology. Here we studied the electrophysiological properties and the transcriptional and translational expression of T lymphocyte Kv1.3 channels in multiple sclerosis, by combining patch clamp recordings, reverse transcription polymerase chain reaction and flow cytometry on freshly isolated peripheral blood T lymphocytes from two patient cohorts with multiple sclerosis, as well as from healthy and disease controls. Our data demonstrate that T lymphocytes in MS, manifest a significant up-regulation of Kv1.3 mRNA, Kv1.3 membrane protein and Kv1.3 current density and therefore of functional membrane channel protein, compared to control groups ( < 0.001). Interestingly, patient sub-grouping shows that Kv1.3 channel density is significantly higher in secondary progressive, compared to relapsing-remitting multiple sclerosis ( < 0.001). Taking into account the tight connection between Kv1.3 channel activity and calcium-dependent processes, our data predict and could partly explain the reported alterations of T lymphocyte function in multiple sclerosis, while they highlight Kv1.3 channels as potential therapeutic targets and peripheral biomarkers for the disease.
电压门控性Kv1.3钾通道是T淋巴细胞激活、增殖和细胞因子产生的关键调节因子,它能在免疫刺激后为钙内流提供必要的膜超极化。值得注意的是,越来越多的证据将这些通道与多发性硬化症的病理生理学联系起来。在这里,我们通过对来自两个多发性硬化症患者队列以及健康和疾病对照的新鲜分离的外周血T淋巴细胞进行膜片钳记录、逆转录聚合酶链反应和流式细胞术,研究了多发性硬化症中T淋巴细胞Kv1.3通道的电生理特性以及转录和翻译表达。我们的数据表明,与对照组相比(<0.001),多发性硬化症患者的T淋巴细胞中Kv1.3 mRNA、Kv1.细胞膜蛋白和Kv1.3电流密度以及功能性膜通道蛋白均显著上调。有趣的是,患者亚组分析显示,与复发缓解型多发性硬化症相比,继发进展型多发性硬化症中Kv1.3通道密度显著更高(<0.001)。考虑到Kv1.3通道活性与钙依赖性过程之间的紧密联系,我们的数据预测并可以部分解释多发性硬化症中报道的T淋巴细胞功能改变,同时突出了Kv1.3通道作为该疾病潜在治疗靶点和外周生物标志物的地位。