Neuroscience Program, Smith College, Northampton, MA 01063, USA.
Int J Mol Sci. 2022 Apr 5;23(7):4028. doi: 10.3390/ijms23074028.
Recent studies have shed light on the diverse and complex roles of G-protein coupled receptors (GPCRs) in the pathophysiology of stroke. These receptors constitute a large family of seven transmembrane-spanning proteins that play an intricate role in cellular communication mechanisms which drive both tissue injury and repair following ischemic stroke. Orphan GPCRs represent a unique sub-class of GPCRs for which no natural ligands have been found. Interestingly, the majority of these receptors are expressed within the central nervous system where they represent a largely untapped resource for the treatment of neurological diseases. The focus of this review will thus be on the emerging roles of two brain-expressed orphan GPCRs, GPR37 and GPR37 L1, in regulating various cellular and molecular processes underlying ischemic stroke.
最近的研究揭示了 G 蛋白偶联受体(GPCR)在中风病理生理学中的多样而复杂的作用。这些受体构成了一个大型的七跨膜蛋白家族,在细胞通讯机制中发挥着复杂的作用,这些机制既驱动了缺血性中风后的组织损伤,也驱动了组织修复。孤儿 GPCR 是 GPCR 的一个独特亚类,尚未发现其天然配体。有趣的是,这些受体中的大多数在中枢神经系统中表达,它们代表了治疗神经疾病的一个尚未充分利用的资源。因此,本综述的重点将放在两个在大脑中表达的孤儿 GPCR,GPR37 和 GPR37L1,在调节缺血性中风下各种细胞和分子过程中的新兴作用上。