Soto Enrique, Ortega-Ramírez Audrey, Vega Rosario
Instituto de Fisiología, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.
Front Cell Neurosci. 2018 Oct 10;12:342. doi: 10.3389/fncel.2018.00342. eCollection 2018.
In this review, evidence demonstrating that protons (H) constitute a complex, regulated intercellular signaling mechanisms are presented. Given that pH is a strictly regulated variable in multicellular organisms, localized extracellular pH changes may constitute significant signals of cellular processes that occur in a cell or a group of cells. Several studies have demonstrated that the low pH of synaptic vesicles implies that neurotransmitter release is always accompanied by the co-release of H into the synaptic cleft, leading to transient extracellular pH shifts. Also, evidence has accumulated indicating that extracellular H concentration regulation is complex and implies a source of protons in a network of transporters, ion exchangers, and buffer capacity of the media that may finally establish the extracellular proton concentration. The activation of membrane transporters, increased production of CO and of metabolites, such as lactate, produce significant extracellular pH shifts in nano- and micro-domains in the central nervous system (CNS), constituting a reliable signal for intercellular communication. The acid sensing ion channels (ASIC) function as specific signal sensors of proton signaling mechanism, detecting subtle variations of extracellular H in a range varying from pH 5 to 8. The main question in relation to this signaling system is whether it is only synaptically restricted, or a volume modulator of neuron excitability. This signaling system may have evolved from a metabolic activity detection mechanism to a highly localized extracellular proton dependent communication mechanism. In this study, evidence showing the mechanisms of regulation of extracellular pH shifts and of the ASICs and its function in modulating the excitability in various systems is reviewed, including data and its role in synaptic neurotransmission, volume transmission and even segregated neurotransmission, leading to a reliable extracellular signaling mechanism.
在本综述中,展示了质子(H⁺)构成复杂且受调控的细胞间信号传导机制的证据。鉴于pH值在多细胞生物中是一个严格调控的变量,局部细胞外pH值变化可能构成细胞或一组细胞中发生的细胞过程的重要信号。多项研究表明,突触小泡的低pH值意味着神经递质释放总是伴随着H⁺共同释放到突触间隙,导致细胞外pH值短暂变化。此外,已有证据表明细胞外H⁺浓度调节很复杂,意味着在转运体、离子交换体网络以及最终可能决定细胞外质子浓度的介质缓冲能力中存在质子来源。膜转运体的激活、CO和代谢产物(如乳酸)产量的增加,会在中枢神经系统(CNS)的纳米和微区产生显著的细胞外pH值变化,构成细胞间通讯的可靠信号。酸敏感离子通道(ASIC)作为质子信号传导机制的特定信号传感器,可检测细胞外H⁺在pH 5至8范围内的细微变化。与该信号系统相关的主要问题是,它是否仅受突触限制,还是神经元兴奋性的容积调节因子。该信号系统可能已从代谢活动检测机制演变为高度局部化的细胞外质子依赖性通讯机制。在本研究中,回顾了显示细胞外pH值变化调节机制、ASIC及其在调节各种系统兴奋性中的功能的证据,包括其在突触神经传递、容积传递甚至分离神经传递中的数据及其作用,从而形成一种可靠的细胞外信号传导机制。