评估神经元初级纤毛电化学信号的方法

IF 4.5 2区 生物学 Q2 CELL BIOLOGY
Paul G. DeCaen, Louise F. Kimura
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引用次数: 0

摘要

初级纤毛是从极化细胞的顶端突出的多模感觉细胞器。它们存在于所有的大脑半球,但在神经元中最为明显,神经元由海马和小脑的颗粒层组成。编码初级纤毛成分的基因的致病性变异是神经性纤毛病的原因。神经性纤毛病是一组中枢神经系统疾病,以智力残疾、癫痫、共济失调和感觉缺陷等神经发育状况为特征。在海马中,神经元初级纤毛与轴突形成化学突触,它们的膜上充满了独特的离子通道和G蛋白偶联受体(gpcr)。初级纤毛是小而特殊的隔室,对细胞器的研究具有挑战性。详细地,我们描述了纤毛电生理学方法和使用纤毛特异性荧光传感器来测定神经元多囊素通道功能和血清素能受体信号传导。这些工具使研究人员能够实时和半定量地分析孤立神经元中的钙、cAMP和通道相关信号通路,同时增强我们对这种未被研究的细胞器及其在纤毛病疾病状态中的失调的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Methods to Assess Neuronal Primary Cilia Electrochemical Signaling

Methods to Assess Neuronal Primary Cilia Electrochemical Signaling

Primary cilia are polymodal sensory organelles which project from the apical side of polarized cells. They are found in all brain hemispheres but are most pronounced in neurons, which comprise the granular layers of the hippocampus and cerebellum. Pathogenic variants in genes which encode primary cilia components are responsible for neuronal ciliopathies—a group of central nervous system disorders characterized by neurodevelopmental conditions such as intellectual disability, seizure, ataxia, and sensory deficits. In the hippocampus, neuronal primary cilia form chemical synapses with axons and their membranes are populated with unique sets of ion channels and G protein-coupled receptors (GPCRs). Primary cilia are small and privileged compartments that are challenging organelles to study. In detail, we describe cilia electrophysiology methods and the use of cilia-specific fluorescent sensors to assay neuronal polycystin channel function and serotonergic receptor signaling, respectively. These tools allow researchers to assay calcium, cAMP and channel-related signaling pathways in isolated neurons in real-time and in semi-quantitative terms, while enhancing our understanding of this understudied organelle and its dysregulation in ciliopathy disease states.

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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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