Department of Pharmacology, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4965, USA.
Annu Rev Neurosci. 2013 Jul 8;36:139-64. doi: 10.1146/annurev-neuro-062012-170313. Epub 2013 May 15.
G protein-coupled receptors (GPCRs) are essential mediators of signal transduction, neurotransmission, ion channel regulation, and other cellular events. GPCRs are activated by diverse stimuli, including light, enzymatic processing of their N-termini, and binding of proteins, peptides, or small molecules such as neurotransmitters. GPCR dysfunction caused by receptor mutations and environmental challenges contributes to many neurological diseases. Moreover, modern genetic technology has helped identify a rich array of mono- and multigenic defects in humans and animal models that connect such receptor dysfunction with disease affecting neuronal function. The visual system is especially suited to investigate GPCR structure and function because advanced imaging techniques permit structural studies of photoreceptor neurons at both macro and molecular levels that, together with biochemical and physiological assessment in animal models, provide a more complete understanding of GPCR signaling.
G 蛋白偶联受体 (GPCRs) 是信号转导、神经递质传递、离子通道调节和其他细胞事件的重要介质。GPCRs 可被多种刺激激活,包括光、N 端的酶处理和蛋白质、肽或小分子(如神经递质)的结合。受体突变和环境挑战引起的 GPCR 功能障碍导致许多神经疾病。此外,现代遗传技术帮助鉴定了人类和动物模型中丰富的单基因和多基因缺陷,这些缺陷将这种受体功能障碍与影响神经元功能的疾病联系起来。视觉系统特别适合研究 GPCR 的结构和功能,因为先进的成像技术允许在宏观和分子水平上对光感受器神经元进行结构研究,结合动物模型中的生化和生理学评估,提供对 GPCR 信号转导的更全面理解。