Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Italy.
FEBS Lett. 2022 Sep;596(18):2364-2381. doi: 10.1002/1873-3468.14441. Epub 2022 Jul 10.
Deregulated metabolism is a well-known feature of several challenging diseases, including diabetes, obesity and cancer. Besides their important role as intracellular bioenergetic molecules, dietary nutrients and metabolic intermediates are released in the extracellular environment. As such, they may achieve unconventional roles as hormone-like molecules by activating cell surface G-protein-coupled receptors (GPCRs) that regulate several pathophysiological processes. In this review, we provide an insight into the role of lactate, succinate, fatty acids, amino acids as well as ketogenesis-derived and β-oxidation-derived intermediates as extracellular signalling molecules. Moreover, the mechanisms by which their cognate metabolite-sensing GPCRs integrate nutritional and metabolic signals with specific intracellular pathways will be described. A better comprehension of these aspects is of fundamental importance to identify GPCRs as novel druggable targets.
代谢失调是包括糖尿病、肥胖症和癌症在内的多种棘手疾病的显著特征。除了作为细胞内生物能量分子的重要作用外,膳食营养素和代谢中间产物也会释放到细胞外环境中。因此,它们可能通过激活细胞表面 G 蛋白偶联受体(GPCR)发挥非传统的激素样分子作用,调节多种病理生理过程。在这篇综述中,我们深入探讨了乳酸盐、琥珀酸盐、脂肪酸、氨基酸以及酮体生成和β氧化衍生中间产物作为细胞外信号分子的作用。此外,还将描述其同源代谢物感应 GPCR 将营养和代谢信号与特定的细胞内途径整合的机制。更好地理解这些方面对于将 GPCR 鉴定为新型可药物靶标至关重要。