Montreal Heart Institute, Montréal, Québec H1T 1C8, Canada; Departments of Biochemistry and Molecular Medicine, Medicine, Pharmacology and Physiology, Université de Montréal, Montréal, Québec H3T 1J4, Canada.
Montreal Heart Institute, Montréal, Québec H1T 1C8, Canada.
Cell Signal. 2024 Nov;123:111358. doi: 10.1016/j.cellsig.2024.111358. Epub 2024 Aug 22.
G protein-coupled receptors (GPCRs) have historically been associated with signalling events driven from the plasma membrane. More recently, signalling from endosomes has been recognized as a feature of internalizing receptors. However, there was little consideration given to the notion that GPCRs can be targeted to distinct subcellular locations that did not involve an initial trafficking to the cell surface. Here, we focus on the evidence for and the potential impact of GPCR signalling specifically initiated from the nuclear membrane. We also discuss the possibilities for selectively targeting this and other internal pools of receptors as novel venues for drug discovery.
G 蛋白偶联受体(GPCRs)传统上与来自质膜的信号事件有关。最近,内体的信号转导已被认为是内吞受体的一个特征。然而,很少有人考虑到 GPCR 可以被靶向到不涉及最初向细胞表面运输的不同亚细胞位置的概念。在这里,我们重点介绍从核膜特异性启动的 GPCR 信号转导的证据及其潜在影响。我们还讨论了靶向这种和其他内部受体库的可能性,作为药物发现的新途径。