Department of Gastroenterology and Hepatology, University Hospital Zurich, University of Zurich, 8091, Zurich, CH, Switzerland.
Pflugers Arch. 2024 Apr;476(4):611-622. doi: 10.1007/s00424-024-02943-y. Epub 2024 Mar 22.
Low pH in the gut is associated with severe inflammation, fibrosis, and colorectal cancer (CRC) and is a hallmark of active inflammatory bowel disease (IBD). Subsequently, pH-sensing mechanisms are of interest for the understanding of IBD pathophysiology. Tissue hypoxia and acidosis-two contributing factors to disease pathophysiology-are linked to IBD, and understanding their interplay is highly relevant for the development of new therapeutic options. One member of the proton-sensing G protein-coupled receptor (GPCR) family, GPR65 (T-cell death-associated gene 8, TDAG8), was identified as a susceptibility gene for IBD in a large genome-wide association study. In response to acidic extracellular pH, GPR65 induces an anti-inflammatory response, whereas the two other proton-sensing receptors, GPR4 and GPR68 (ovarian cancer G protein-coupled receptor 1, OGR1), mediate pro-inflammatory responses. Here, we review the current knowledge on the role of these proton-sensing receptors in IBD and IBD-associated fibrosis and cancer, as well as colitis-associated cancer (CAC). We also describe emerging small molecule modulators of these receptors as therapeutic opportunities for the treatment of IBD.
肠道内的低 pH 值与严重的炎症、纤维化和结直肠癌(CRC)有关,是活动性炎症性肠病(IBD)的标志。因此,pH 感应机制是理解 IBD 病理生理学的关键。组织缺氧和酸中毒——两种导致疾病病理生理学的因素——与 IBD 有关,了解它们之间的相互作用对于开发新的治疗选择非常重要。质子感应 G 蛋白偶联受体(GPCR)家族的一个成员,GPR65(T 细胞死亡相关基因 8,TDAG8),在一项大型全基因组关联研究中被确定为 IBD 的易感基因。当细胞外 pH 值降低时,GPR65 会引发抗炎反应,而另外两个质子感应受体,GPR4 和 GPR68(卵巢癌 G 蛋白偶联受体 1,OGR1),则介导促炎反应。在这里,我们回顾了这些质子感应受体在 IBD 及其相关纤维化和癌症以及结肠炎相关癌症(CAC)中的作用的最新知识。我们还描述了这些受体的新兴小分子调节剂,作为治疗 IBD 的治疗机会。