Centre for Neuroendocrinology, Faculty of Health Sciences, University of Pretoria, Private Bag X323, Pretoria 0031, South Africa.
Department of Physiology, Faculty of Health Sciences, University of Pretoria, Private Bag X323, Pretoria 0031, South Africa.
Int J Mol Sci. 2022 Apr 21;23(9):4587. doi: 10.3390/ijms23094587.
G protein-coupled receptors (GPCRs) facilitate the majority of signal transductions across cell membranes in humans, with numerous diseases attributed to inactivating GPCR mutations. Many of these mutations result in misfolding during nascent receptor synthesis in the endoplasmic reticulum (ER), resulting in intracellular retention and degradation. Pharmacological chaperones (PCs) are cell-permeant small molecules that can interact with misfolded receptors in the ER and stabilise/rescue their folding to promote ER exit and trafficking to the cell membrane. The neurokinin 3 receptor (NK3R) plays a pivotal role in the hypothalamic-pituitary-gonadal reproductive axis. We sought to determine whether NK3R missense mutations result in a loss of cell surface receptor expression and, if so, whether a cell-permeant small molecule NK3R antagonist could be repurposed as a PC to restore function to these mutants. Quantitation of cell surface expression levels of seven mutant NK3Rs identified in hypogonadal patients indicated that five had severely impaired cell surface expression. A small molecule NK3R antagonist, M8, increased cell surface expression in four of these five and resulted in post-translational receptor processing in a manner analogous to the wild type. Importantly, there was a significant improvement in receptor activation in response to neurokinin B (NKB) for all four receptors following their rescue with M8. This demonstrates that M8 may have potential for therapeutic development in the treatment of hypogonadal patients harbouring NK3R mutations. The repurposing of existing small molecule GPCR modulators as PCs represents a novel and therapeutically viable option for the treatment of disorders attributed to mutations in GPCRs that cause intracellular retention.
G 蛋白偶联受体(GPCRs)在人体中促进了大多数跨细胞膜的信号转导,许多疾病归因于 GPCR 突变失活。这些突变中的许多在新生受体在内质网(ER)中合成时导致错误折叠,导致细胞内滞留和降解。药理学伴侣(PCs)是细胞渗透性的小分子,可与 ER 中的错误折叠受体相互作用并稳定/挽救其折叠,以促进 ER 出口和转运至细胞膜。神经激肽 3 受体(NK3R)在下丘脑-垂体-性腺生殖轴中发挥关键作用。我们试图确定 NK3R 错义突变是否导致细胞表面受体表达丧失,如果是这样,是否可以将细胞渗透性小分子 NK3R 拮抗剂重新用作 PC 来恢复这些突变体的功能。定量分析在性腺功能减退患者中鉴定的七个突变 NK3R 的细胞表面表达水平表明,其中五个具有严重的细胞表面表达受损。一种小分子 NK3R 拮抗剂 M8 增加了其中五个中的四个的细胞表面表达,并以类似于野生型的方式导致受体的翻译后加工。重要的是,在用 M8 拯救后,所有四个受体对神经激肽 B(NKB)的受体激活均有显著改善。这表明 M8 可能有潜力用于治疗携带 NK3R 突变的性腺功能减退患者。将现有的小分子 GPCR 调节剂重新用作 PC 代表了一种治疗由于 GPCR 突变导致细胞内滞留而引起的疾病的新型和可行的治疗选择。