G蛋白偶联受体
受体
突变体
兴奋剂
化学
HEK 293细胞
葡萄糖稳态
野生型
细胞生物学
胰高血糖素样肽1受体
信号转导
细胞表面受体
内分泌学
肠促胰岛素
生物
化学伴侣
细胞
小分子
生物化学
内科学
细胞信号
G蛋白
伴侣(临床)
细胞膜
胰高血糖素受体
作者
Ya‐Xiong Tao,Shuangyu Lian,Florence Gbahou,Julie Dam,Ralf Jockers
标识
DOI:10.1210/jendso/bvaf149.1231
摘要
Abstract Disclosure: Y. Tao: None. S. Lian: None. F. Gbahou: None. J. Dam: None. R. Jockers: None. Glucagon-like peptide 1 (GLP1) is an incretin hormone released in response to food intake and increase in blood glucose. GLP1 regulates glucose homeostasis via its membrane receptor, GLP1R, a member of G protein-coupled receptor (GPCR) superfamily. GLP1R typically activates the cAMP signaling pathway to promote insulin secretion. We recently showed that many naturally occurring variants in GLP1R that are associated with increased adiposity and impaired glucose balance have decreased cell surface expression (Gao W. et al., 2023. Nature Metabolism 5:1673-1684). Pharmacological chaperone (pharmacoperone) are small molecule lipophilic ligands that can bind to the misfolded mutants retained intracellularly and facilitate the folding and anterograde trafficking of the mutants. Pharmacoperones have been identified for mutant GPCRs associated with several diseases, including endocrine diseases such as nephrogenic diabetes insipidus, obesity, and hypogonadism. In this study, we identified a small molecule GLP1R agonist, in Class III clinical trials, as a potent pharmacoperone. In HEK293 cells, cell surface expression was increased in most of the 21 mutants tested, and some mutants increased up to 20-fold, reaching that of the wild-type (WT) GLP1R. Indeed, the cell surface expression of the WT GLP1R was also increased, suggesting that the folding of the WT GLP1R was not optimal and could be enhanced. Total expression of these receptors was not affected. We further showed that a 24h, but not an acute, treatment with the small molecule GLP1R agonist increased cAMP production of several mutants. Some of them also became responsive to additional GLP1(7-36) stimulation. We then expressed the mutant receptors in INS-1 insulinoma cells lacking endogenous GLP1R. A 24h treatment with the small molecule GLP1R agonist restored GLP1(7-36)-induced insulin secretion in these cells for at least five GLP1R mutants. In summary, we identified a small molecule GLP1R agonist as a pharmacoperone rescuing impaired insulin secretion of natural GLP1R mutants. This can become a potential precision medicine strategy for treatment patients with T2DM due to GLP1R mutations. Presentation: Sunday, July 13, 2025
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