University of Texas Health Science Center at San Antonio, Department of Cellular and Integrative Physiology, San Antonio, TX, 78229, USA.
Xiangya School of Medicine, Central South University, Changsha, Hunan, China.
Sci Rep. 2019 Nov 13;9(1):16683. doi: 10.1038/s41598-019-53087-4.
Many neurons, including cerebellar granule cells, exhibit a tonic GABA current mediated by extrasynaptic GABA receptors. This current is a critical regulator of firing and the target of many clinically relevant compounds. Using a combination of patch clamp electrophysiology and photolytic uncaging of RuBi-GABA we show that GABA receptors are tonically active and enhance extrasynaptic GABA receptor currents in cerebellar granule cells. This enhancement is not associated with meaningful changes in GABA receptor potency, mean channel open-time, open probability, or single-channel current. However, there was a significant (~40%) decrease in the number of channels participating in the GABA uncaging current and an increase in receptor desensitization. Furthermore, we find that adenylate cyclase, PKA, CaMKII, and release of Ca from intracellular stores are necessary for modulation of GABA receptors. Overall, this work reveals crosstalk between postsynaptic GABA and GABA receptors and identifies the signaling pathways and mechanisms involved.
许多神经元,包括小脑颗粒细胞,表现出由突触外 GABA 受体介导的紧张性 GABA 电流。该电流是放电的关键调节剂,也是许多具有临床相关性的化合物的作用靶点。我们使用膜片钳电生理学和 RuBi-GABA 的光解离技术相结合,表明 GABA 受体处于紧张状态,并增强小脑颗粒细胞中的突触外 GABA 受体电流。这种增强与 GABA 受体效力、平均通道开放时间、开放概率或单通道电流没有明显变化相关。然而,参与 GABA 光解电流的通道数量显著减少(约 40%),受体脱敏增加。此外,我们发现腺苷酸环化酶、PKA、CaMKII 和细胞内储存的 Ca 释放对于 GABA 受体的调节是必需的。总的来说,这项工作揭示了突触后 GABA 和 GABA 受体之间的串扰,并确定了涉及的信号通路和机制。