Inserm Unité 901 Marseille, France ; Aix-Marseille Université Marseille, France ; INMED Marseille, France.
Front Mol Neurosci. 2013 Apr 10;6:7. doi: 10.3389/fnmol.2013.00007. eCollection 2013.
Chloride (Cl(-)) homeostasis is known to be fundamental for central nervous system functioning. Alterations in intracellular Cl(-) concentration ([Cl(-)]i) and changes in the efficacy of Cl(-) extrusion are involved in numerous neurological disorders. Therefore, there is a strong need for studies of the dynamics of [Cl(-)]i in different cell types under physiological conditions and during pathology. Several previous works reported having successfully achieved recording of [Cl(-)]i using genetically encoded Cl-Sensor that is composed of the cyan fluorescent protein (CFP) and Cl(-)-sensitive mutant of the yellow fluorescent protein (YFPCl). However, all reported works were performed using specially designed setups with ultra-sensitive CCD cameras. Our multiple attempts to monitor Cl(-)-dependent fluorescence of Cl-Sensor using conventional epifluorescence microscopes did not yield successful results. In the present work, we have analysed the reason of our failures and found that they were caused by a strong inactivation of the YFPCl component of Cl-Sensor during excitation of the CFP with 430 nm light. Based on the obtained results, we reduced 20-fold the intensity of the 430 nm excitation and modified the recording protocol that allows now stable long-lasting ratiometric measurements of Cl-Sensor fluorescence in different cell types including cultured hippocampal neurons and their tiny dendrites and spines. Simultaneous imaging and patch clamp recording revealed that in mature neurons, the novel protocol allows detection of as little as 2 mM changes of [Cl(-)]i from the resting level of 5-10 mM. We demonstrate also a usefulness of the developed [Cl(-)]i measurement procedure for large scale screening of the activity of exogenously expressed potassium-chloride co-transporter KCC2, a major neuronal Cl(-) extruder that is implicated in numerous neurological disorders and is a target for novel therapeutical treatments.
氯离子(Cl(-))稳态对于中枢神经系统的功能至关重要。细胞内氯离子浓度 ([Cl(-)]i) 的改变和氯离子外排效率的变化与许多神经疾病有关。因此,强烈需要研究生理条件下和病理状态下不同细胞类型中 [Cl(-)]i 的动力学。以前的几项工作报道了使用由青色荧光蛋白(CFP)和氯离子敏感型黄色荧光蛋白(YFPCl)突变体组成的基因编码氯离子传感器(Cl-Sensor)成功地实现了 [Cl(-)]i 的记录。然而,所有报道的工作都是使用具有超灵敏 CCD 相机的特殊设计的设备进行的。我们多次尝试使用常规荧光显微镜监测 Cl-Sensor 的氯离子依赖性荧光,但均未获得成功结果。在本工作中,我们分析了失败的原因,发现这是由于 430nm 光激发 CFP 时 Cl-Sensor 的 YFPCl 部分强烈失活所致。基于获得的结果,我们将 430nm 激发的强度降低了 20 倍,并修改了记录方案,现在可以稳定地进行不同细胞类型(包括培养的海马神经元及其微小的树突和棘突)中 Cl-Sensor 荧光的长时比测量。同时的成像和膜片钳记录表明,在成熟神经元中,新的方案允许检测到 [Cl(-)]i 从 5-10mM 的静息水平仅变化 2mM。我们还证明了开发的 [Cl(-)]i 测量程序对于体外表达的钾氯离子共转运体 KCC2 的活性的大规模筛选是有用的,KCC2 是一种主要的神经元氯离子外排器,与许多神经疾病有关,是新的治疗靶点。