首页> 外文期刊>The Journal of Physiology >Integration of K+ and Cl- currents regulate steady-state and dynamic membrane potentials in cultured rat microglia.
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Integration of K+ and Cl- currents regulate steady-state and dynamic membrane potentials in cultured rat microglia.

机译:K +和Cl-电流的整合调节了培养的大鼠小胶质细胞的稳态和动态膜电位。

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摘要

The role of ion channels and membrane potential (V(m)) in non-excitable cells has recently come under increased scrutiny. Microglia, the brain's resident immune cells, express voltage-gated Kv1.3 channels, a Kir2.1-like inward rectifier, a swelling-activated Cl(-) current and several other channels. We previously showed that Kv1.3 and Cl(-) currents are needed for microglial cell proliferation and that Kv1.3 is important for the respiratory burst. Although their mechanisms of action are unknown, one general role for these channels is to maintain a negative V(m). An impediment to measuring V(m) in non-excitable cells is that many have a very high electrical resistance, which makes them extremely susceptible to leak-induced depolarization. Using non-invasive V(m)-sensitive dyes, we show for the first time that the membrane resistance of microglial cells is several gigaohms; much higher than the seal resistance during patch-clamp recordings. Surprisingly, we observed that small current injections can evoke large V(m) oscillations in some microglial cells, and that injection of sinusoidal currents of varying frequency exposes a strong intrinsic electrical resonance in the 5- to 20-Hz frequency range in all microglial cells tested. Using a dynamic current clamp that we developed to actively compensate for the damage done by the patch-clamp electrode, we found that the V(m) oscillations and resonance were more prevalent and larger. Both types of electrical behaviour required Kv1.3 channels, as they were eliminated by the Kv1.3 blocker, agitoxin-2. To further determine how the ion currents integrate in these cells, voltage-clamp recordings from microglial cells displaying these behaviours were used to analyse the biophysical properties of the Kv1.3, Kir and Cl(-) currents. A mathematical model that incorporated only these three currents reproduced the observed V(m) oscillations and electrical resonance. Thus, the electrical behaviour of this 'non-excitable' cell type is much more complex than previously suspected, and might reflect a more common oversight in high resistance cells.
机译:离子通道和膜电位(V(m))在非兴奋性细胞中的作用最近受到了越来越多的审查。小胶质细胞,大脑的常驻免疫细胞,表达电压门控的Kv1.3通道,类似Kir2.1的内向整流器,溶胀激活的Cl(-)电流和其他几个通道。我们以前表明,Kv1.3和Cl(-)电流对于小胶质细胞增殖是必需的,并且Kv1.3对于呼吸爆发很重要。尽管它们的作用机理尚不清楚,但这些通道的一般作用是维持负V(m)。测量非激励单元的V(m)的障碍是许多单元具有很高的电阻,这使得它们极易受到泄漏引起的去极化作用。使用非侵入性的V(m)敏感染料,我们首次表明小胶质细胞的膜电阻为几千兆欧;远高于膜片钳记录期间的密封电阻。出乎意料的是,我们观察到小电流注入会在某些小胶质细胞中引起大的V(m)振荡,而不同频率的正弦电流注入会在所有小胶质细胞的5至20 Hz频率范围内暴露出强大的固有共振。经过测试。使用我们开发的动态电流钳来主动补偿膜片钳电极造成的损坏,我们发现V(m)的振荡和谐振更为普遍和较大。两种类型的电气行为都需要Kv1.3通道,因为它们被Kv1.3阻断剂agitoxin-2消除了。为了进一步确定离子电流如何在这些细胞中整合,来自显示这些行为的小胶质细胞的电压钳记录用于分析Kv1.3,Kir和Cl(-)电流的生物物理特性。仅包含这三个电流的数学模型再现了观察到的V(m)振荡和电谐振。因此,这种“非激励”电池的电性能比以前怀疑的要复杂得多,并且可能反映了高电阻电池中更常见的疏忽。

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