Department of Biochemistry, Weill Cornell Medicine, New York, NY 10065, USA.
Department of Biochemistry, Weill Cornell Medicine, New York, NY 10065, USA; Department of Psychiatry, Weill Cornell Medicine, New York, NY 10065, USA.
Trends Neurosci. 2024 Aug;47(8):635-650. doi: 10.1016/j.tins.2024.05.008. Epub 2024 Jun 11.
In the nervous system, G protein-coupled receptors (GPCRs) control neuronal excitability, synaptic transmission, synaptic plasticity, and, ultimately, behavior through spatiotemporally precise initiation of a variety of signaling pathways. However, despite their critical importance, there is incomplete understanding of how these receptors are regulated to tune their signaling to specific neurophysiological contexts. A deeper mechanistic picture of neuromodulatory GPCR function is needed to fully decipher their biological roles and effectively harness them for the treatment of neurological and psychiatric disorders. In this review, we highlight recent progress in identifying novel modes of regulation of neuromodulatory GPCRs, including G protein- and receptor-targeting mechanisms, receptor-receptor crosstalk, and unique features that emerge in the context of chemical synapses. These emerging principles of neuromodulatory GPCR tuning raise critical questions to be tackled at the molecular, cellular, synaptic, and neural circuit levels in the future.
在神经系统中,G 蛋白偶联受体 (GPCR) 通过时空精确启动各种信号通路来控制神经元兴奋性、突触传递、突触可塑性,最终控制行为。然而,尽管这些受体至关重要,但对于如何调节它们的信号以适应特定的神经生理环境,我们的理解并不完全。为了充分破译它们的生物学作用并有效地将它们用于治疗神经和精神疾病,需要对神经调节 GPCR 功能有更深入的机械论认识。在这篇综述中,我们强调了识别神经调节 GPCR 新调节模式的最新进展,包括 G 蛋白和受体靶向机制、受体-受体串扰以及在化学突触背景下出现的独特特征。这些新兴的神经调节 GPCR 调节原则提出了在未来需要在分子、细胞、突触和神经回路水平上解决的关键问题。