Leyton Paula, Riquelme Denise, Peralta Francisco A, Navarro Franco D, Leiva-Salcedo Elias
Department of Biology, Faculty of Chemistry and Biology, University of Santiago, Santiago, Chile.
Front Cell Dev Biol. 2024 Jul 23;12:1440140. doi: 10.3389/fcell.2024.1440140. eCollection 2024.
TRPM4 is a calcium activated non-selective cation channel, impermeable to Ca, in neurons it has been implicated in the regulation of the excitability and in the persistent firing. Cholinergic stimulation is also implicated in changes in excitability that leads neurons to an increased firing frequency, however it is not clear whether TRPM4 is involved in the cholinergic-induced increase in firing frequency. Here using a combination of patch clamp electrophysiology, Ca imaging, immunofluorescence, fluorescence recovery after photobleaching (FRAP) and pharmacological approach, we demonstrate that carbachol (Cch) increases firing frequency, intracellular Ca and that TRPM4 inhibition using 9-Ph and CBA reduces firing frequency and decreases the peak in intracellular Ca induced by Cch in cortical pyramidal neurons in culture. Moreover, we determined that cholinergic stimulation reduces TRPM4 recycling and stabilizes TRPM4 in the plasma membrane. Together our results indicate that cholinergic stimulation increases firing in a TRPM4 dependent manner, and also increases the TRPM4 stability in the membrane, suggesting that TRPM4 is locked in microdomains in the membrane, possibly signaling or cytoskeleton proteins complexes.
瞬时受体电位通道蛋白4(TRPM4)是一种钙激活的非选择性阳离子通道,对钙离子不通透,在神经元中,它与兴奋性调节和持续性放电有关。胆碱能刺激也与兴奋性变化有关,这种变化会导致神经元放电频率增加,然而尚不清楚TRPM4是否参与胆碱能诱导的放电频率增加。在这里,我们结合膜片钳电生理学、钙成像、免疫荧光、光漂白后荧光恢复(FRAP)和药理学方法,证明卡巴胆碱(Cch)增加了放电频率、细胞内钙离子浓度,并且使用9-苯基菲啶(9-Ph)和氯苯氨丁酸(CBA)抑制TRPM4可降低培养的皮质锥体神经元的放电频率,并降低Cch诱导的细胞内钙离子峰值。此外,我们确定胆碱能刺激减少了TRPM4的再循环,并使TRPM4在质膜中稳定。我们的结果共同表明,胆碱能刺激以TRPM4依赖的方式增加放电,并增加TRPM4在膜中的稳定性,这表明TRPM4锁定在膜中的微结构域中,可能是信号或细胞骨架蛋白复合物。