Red de Apoyo a la Investigación, Universidad Nacional Autónoma de México and Instituto Nacional de Ciencias Médicas y Nutrición SZ, Mexico City 14080, Mexico.
Departamento de Recursos de la Tierra, Universidad Autónoma Metropolitana-Lerma, Lerma de Villada 52005, Estado de México, Mexico.
Int J Mol Sci. 2021 Nov 15;22(22):12329. doi: 10.3390/ijms222212329.
Misfolding of G protein-coupled receptors (GPCRs) caused by mutations frequently leads to disease due to intracellular trapping of the conformationally abnormal receptor. Several endocrine diseases due to inactivating mutations in GPCRs have been described, including X-linked nephrogenic diabetes insipidus, thyroid disorders, familial hypocalciuric hypercalcemia, obesity, familial glucocorticoid deficiency [melanocortin-2 receptor, MC2R (also known as adrenocorticotropin receptor, ACTHR), and reproductive disorders. In these mutant receptors, misfolding leads to endoplasmic reticulum retention, increased intracellular degradation, and deficient trafficking of the abnormal receptor to the cell surface plasma membrane, causing inability of the receptor to interact with agonists and trigger intracellular signaling. In this review, we discuss the mechanisms whereby mutations in GPCRs involved in endocrine function in humans lead to misfolding, decreased plasma membrane expression of the receptor protein, and loss-of-function diseases, and also describe several experimental approaches employed to rescue trafficking and function of the misfolded receptors. Special attention is given to misfolded GPCRs that regulate reproductive function, given the key role played by these particular membrane receptors in sexual development and fertility, and recent reports on promising therapeutic interventions targeting trafficking of these defective proteins to rescue completely or partially their normal function.
G 蛋白偶联受体 (GPCR) 的错误折叠由突变引起,常导致受体构象异常的细胞内捕获,从而引发疾病。已经描述了几种由于 GPCR 失活突变引起的内分泌疾病,包括 X 连锁肾性尿崩症、甲状腺疾病、家族性低钙性高钙血症、肥胖症、家族性糖皮质激素缺乏症[黑素皮质素-2 受体 (MC2R) (也称为促肾上腺皮质激素受体 (ACTHR)) 和生殖障碍。在这些突变受体中,错误折叠导致内质网滞留、细胞内降解增加以及异常受体向细胞表面质膜的转运缺陷,从而导致受体无法与激动剂相互作用并触发细胞内信号转导。在这篇综述中,我们讨论了涉及人类内分泌功能的 GPCR 突变导致错误折叠、受体蛋白在质膜上表达减少和功能丧失疾病的机制,并描述了几种用于挽救错误折叠受体转运和功能的实验方法。特别关注调节生殖功能的错误折叠 GPCR,因为这些特定的膜受体在性发育和生育力中起着关键作用,以及最近关于针对这些有缺陷的蛋白质的转运的有希望的治疗干预的报告,以部分或完全挽救其正常功能。