Ran Sha, Pan Liang, Shen Yan
School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, PR China.
School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, PR China.
Gene. 2025 Sep 10;964:149625. doi: 10.1016/j.gene.2025.149625. Epub 2025 Jun 9.
G-protein-coupled receptors (GPCRs) play a pivotal role in mediating responses to various hormones, neurotransmitters, and external stimuli, making them essential therapeutic targets for multiple conditions. GPR39, an orphan GPCR that detects changes in extracellular Zn levels, is widely expressed in diverse tissues such as the pancreas, gastrointestinal tract, liver, kidneys, skin, adipose tissue, and brain. Recent studies have increasingly highlighted the involvement of GPR39 in the pathogenesis and progression of inflammatory diseases. By activating Gαq, Gαs, and Gα12/13 signaling pathways, GPR39 modulates key inflammatory signaling cascades, including NF-κB and MAPK, thereby inhibiting the release of inflammatory mediators, mitigating tissue damage, promoting cell proliferation, and enhancing tissue repair. Emerging evidence suggests that GPR39 acts as a significant modulator in neuroinflammation, pancreatitis, inflammatory bowel disease, arthritis, and skin wound healing Moreover, investigations into exogenous agonists like TC-G 1008 have further substantiated the therapeutic potential of GPR39 in inflammatory diseases. This review elucidates the molecular mechanisms of GPR39 and its multifaceted roles in inflammatory diseases, explores its prospects as a therapeutic target, and provides a theoretical foundation for future drug development targeting GPR39.
G蛋白偶联受体(GPCRs)在介导对各种激素、神经递质和外部刺激的反应中起关键作用,使其成为多种病症的重要治疗靶点。GPR39是一种检测细胞外锌水平变化的孤儿GPCR,在胰腺、胃肠道、肝脏、肾脏、皮肤、脂肪组织和大脑等多种组织中广泛表达。最近的研究越来越多地强调GPR39参与炎症性疾病的发病机制和进展。通过激活Gαq、Gαs和Gα12/13信号通路,GPR39调节关键的炎症信号级联反应,包括NF-κB和MAPK,从而抑制炎症介质的释放,减轻组织损伤,促进细胞增殖,并增强组织修复。新出现的证据表明,GPR39在神经炎症、胰腺炎、炎症性肠病、关节炎和皮肤伤口愈合中起重要调节作用。此外,对TC-G 1008等外源性激动剂的研究进一步证实了GPR39在炎症性疾病中的治疗潜力。本综述阐明了GPR39的分子机制及其在炎症性疾病中的多方面作用,探讨了其作为治疗靶点前景,并为未来针对GPR39的药物开发提供理论基础。