Department of Neuroscience , Washington University School of Medicine , Saint Louis , Missouri 63110 , United States.
ACS Chem Neurosci. 2018 Sep 19;9(9):2162-2172. doi: 10.1021/acschemneuro.7b00516. Epub 2018 Feb 16.
The trillions of synaptic connections within the human brain are shaped by experience and neuronal activity, both of which underlie synaptic plasticity and ultimately learning and memory. G protein-coupled receptors (GPCRs) play key roles in synaptic plasticity by strengthening or weakening synapses and/or shaping dendritic spines. While most studies of synaptic plasticity have focused on cell surface receptors and their downstream signaling partners, emerging data point to a critical new role for the very same receptors to signal from inside the cell. Intracellular receptors have been localized to the nucleus, endoplasmic reticulum, lysosome, and mitochondria. From these intracellular positions, such receptors may couple to different signaling systems, display unique desensitization patterns, and/or show distinct patterns of subcellular distribution. Intracellular GPCRs can be activated at the cell surface, endocytosed, and transported to an intracellular site or simply activated in situ by de novo ligand synthesis, diffusion of permeable ligands, or active transport of non-permeable ligands. Current findings reinforce the notion that intracellular GPCRs play a dynamic role in synaptic plasticity and learning and memory. As new intracellular GPCR roles are defined, the need to selectively tailor agonists and/or antagonists to both intracellular and cell surface receptors may lead to the development of more effective therapeutic tools.
人类大脑中的数万亿个突触连接是由经验和神经元活动塑造的,这两者都构成了突触可塑性的基础,最终影响学习和记忆。G 蛋白偶联受体(GPCR)通过增强或减弱突触和/或塑造树突棘在突触可塑性中发挥关键作用。虽然大多数关于突触可塑性的研究都集中在细胞表面受体及其下游信号伙伴上,但新出现的数据表明,这些受体从细胞内部发出信号具有至关重要的新作用。细胞内受体已被定位到细胞核、内质网、溶酶体和线粒体。从这些细胞内位置,这些受体可以与不同的信号系统偶联,表现出独特的脱敏模式,和/或显示出不同的细胞内分布模式。细胞内 GPCR 可以在细胞表面被激活,内吞,并被转运到细胞内位置,或者简单地通过从头合成配体、可渗透配体的扩散或非渗透配体的主动转运在原位被激活。目前的发现强化了这样一种观点,即细胞内 GPCR 在突触可塑性和学习记忆中发挥着动态作用。随着新的细胞内 GPCR 作用被定义,有必要选择性地针对细胞内和细胞表面受体定制激动剂和/或拮抗剂,这可能会导致更有效的治疗工具的发展。