Department of Medical Sciences and Public Health, University of Cagliari, Monserrato, Italy.
Department of Electrical and Electronic Engineering, University of Cagliari, Cagliari, Italy.
Inflamm Bowel Dis. 2023 Dec 5;29(12):1981-1989. doi: 10.1093/ibd/izad161.
Inflammatory bowel disease, whose major forms are Crohn's disease and ulcerative colitis, is characterized by chronic inflammation of the gut due to the loss of tolerance toward antigens normally contained in the gut lumen. G protein-coupled receptor (GPR) 120 has gained considerable attention as a potential therapeutic target for metabolic disorders due to its implication in the production of the incretin hormone glucagon-like peptide 1 and the secretion of cholecystokinin. Recent studies have also highlighted the role of GPR120 in regulating immune system activity and inflammation. GPR120, expressed by intestinal epithelial cells, proinflammatory macrophages, enteroendocrine L cells, and CD4+ T cells, suppresses proinflammatory and enhances anti-inflammatory cytokine production, suggesting that GPR120 might have a pivotal role in intestinal inflammation and represent a possible therapeutic target in inflammatory bowel disease. This narrative review aims at summarizing the role of GPR120 in the maintenance of intestinal homeostasis through the analysis of the most recent studies.
炎症性肠病(IBD)主要包括克罗恩病(Crohn's disease)和溃疡性结肠炎(ulcerative colitis),其特征为肠道慢性炎症,这是由于对通常存在于肠腔中的抗原失去耐受性所致。G 蛋白偶联受体(GPR)120 因其参与肠促胰岛素激素胰高血糖素样肽 1(glucagon-like peptide 1)的产生和胆囊收缩素(cholecystokinin)的分泌而成为代谢紊乱的潜在治疗靶点,引起了广泛关注。最近的研究还强调了 GPR120 在调节免疫系统活性和炎症中的作用。GPR120 由肠道上皮细胞、促炎巨噬细胞、肠内分泌 L 细胞和 CD4+T 细胞表达,可抑制促炎细胞因子的产生并增强抗炎细胞因子的产生,这表明 GPR120 可能在肠道炎症中发挥关键作用,并可能成为炎症性肠病的治疗靶点。本综述旨在通过分析最近的研究,总结 GPR120 在维持肠道内稳态中的作用。