Department of Physiology and Pharmacology, Sapienza University, Rome, Italy.
Istituto Italiano di Tecnologia, CLNS@Sapienza, Rome, Italy.
Sci Rep. 2017 Jun 23;7(1):4184. doi: 10.1038/s41598-017-04452-8.
Microglia cells, resident immune cells of the brain, survey brain parenchyma by dynamically extending and retracting their processes. Cl channels, activated in the cellular response to stretch/swelling, take part in several functions deeply connected with microglia physiology, including cell shape changes, proliferation, differentiation and migration. However, the molecular identity and functional properties of these Cl channels are largely unknown. We investigated the properties of swelling-activated currents in microglial from acute hippocampal slices of Cx3cr1 mice by whole-cell patch-clamp and imaging techniques. The exposure of cells to a mild hypotonic medium, caused an outward rectifying current, developing in 5-10 minutes and reverting upon stimulus washout. This current, required for microglia ability to extend processes towards a damage signal, was carried mainly by Cl ions and dependent on intracellular Ca. Moreover, it involved swelling-induced ATP release. We identified a purine-dependent mechanism, likely constituting an amplification pathway of current activation: under hypotonic conditions, ATP release triggered the Ca-dependent activation of anionic channels by autocrine purine receptors stimulation. Our study on native microglia describes for the first time the functional properties of stretch/swelling-activated currents, representing a key element in microglia ability to monitor the brain parenchyma.
小胶质细胞是大脑中常驻的免疫细胞,通过动态地伸展和缩回其突起来监测脑实质。Cl 通道在细胞对拉伸/肿胀的反应中被激活,参与了与小胶质细胞生理学密切相关的多种功能,包括细胞形状变化、增殖、分化和迁移。然而,这些 Cl 通道的分子特征和功能特性在很大程度上是未知的。我们通过全细胞膜片钳和成像技术研究了 Cx3cr1 小鼠急性海马切片中小胶质细胞肿胀激活电流的特性。将细胞暴露于轻度低渗介质中,会引起外向整流电流,该电流在 5-10 分钟内发展,并在刺激冲洗时恢复。这种电流对于小胶质细胞向损伤信号延伸突起的能力是必需的,主要由 Cl 离子携带,并依赖于细胞内 Ca。此外,它涉及肿胀诱导的 ATP 释放。我们确定了一种嘌呤依赖性机制,可能构成电流激活的放大途径:在低渗条件下,ATP 释放通过自分泌嘌呤受体刺激触发 Ca 依赖性阴离子通道的激活。我们对天然小胶质细胞的研究首次描述了拉伸/肿胀激活电流的功能特性,这是小胶质细胞监测脑实质能力的关键要素。