Key Laboratory of Anti-inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Centre of Anti-inflammatory and Immune Medicine, Institute of Clinical Pharmacology, Anhui Medical University, Hefei, Anhui Province, China.
Acta Physiol (Oxf). 2022 Oct;236(2):e13866. doi: 10.1111/apha.13866. Epub 2022 Aug 22.
Human G protein-coupled receptor 56 (GPR56) is encoded by gene ADGRG1 from chromosome 16q21 and is homologously encoded in mice, at chromosome 8. Both 687 and 693 splice forms are present in humans and mice. GPR56 has a 381 amino acid-long N-terminal extracellular segment and a GPCR proteolysis site upstream from the first transmembrane domain. GPR56 is mainly expressed in the heart, brain, thyroid, platelets, and peripheral blood mononuclear cells. Accumulating evidence indicates that GPR56 promotes the formation of myelin sheaths and the development of oligodendrocytes in the cerebral cortex of the central nervous system. Moreover, GPR56 contributes to the development and differentiation of hematopoietic stem cells, induces adipogenesis, and regulates the function of immune cells. The lack of GPR56 leads to nervous system dysfunction, platelet disorders, and infertility. Abnormal expression of GPR56 is related to the malignant transformation and tumor metastasis of several cancers including melanoma, neuroglioma, and gastrointestinal cancer. Metabolic disorders and cardiovascular diseases are also associated with dysregulation of GPR56 expression, and GPR56 is involved in the pharmacological resistance to some antidepressant and cancer drug treatments. In this review, the molecular structure, expression profile, and signal transduction of GPR56 are introduced, and physiological and pathological functions of GRP56 are comprehensively summarized. Attributing to its significant biological functions and its long N-terminal extracellular region that interacts with multiple ligands, GPR56 is becoming an attractive therapeutic target in treating neurological and hematopoietic diseases.
人类 G 蛋白偶联受体 56(GPR56)由染色体 16q21 上的基因 ADGRG1 编码,在小鼠中同源编码于染色体 8 上。人类和小鼠中均存在 687 和 693 种剪接形式。GPR56 具有 381 个氨基酸长的 N 端细胞外段和位于第一个跨膜域上游的 GPCR 蛋白水解位点。GPR56 主要在心脏、大脑、甲状腺、血小板和外周血单核细胞中表达。越来越多的证据表明,GPR56 促进中枢神经系统大脑皮层髓鞘的形成和少突胶质细胞的发育。此外,GPR56 有助于造血干细胞的发育和分化,诱导脂肪生成,并调节免疫细胞的功能。GPR56 的缺失导致神经系统功能障碍、血小板紊乱和不孕。GPR56 的异常表达与黑色素瘤、神经胶质瘤和胃肠道癌等多种癌症的恶性转化和肿瘤转移有关。代谢紊乱和心血管疾病也与 GPR56 表达的失调有关,GPR56 参与了一些抗抑郁药和癌症药物治疗的药理耐药性。本文介绍了 GPR56 的分子结构、表达谱和信号转导,全面总结了 GPR56 的生理和病理功能。由于其重要的生物学功能及其与多个配体相互作用的长 N 端细胞外区,GPR56 正在成为治疗神经和血液系统疾病的有吸引力的治疗靶点。