Mouillac Bernard, Mendre Christiane
CNRS UMR 5203, Institut de Génomique Fonctionnelle, F-34000 Montpellier, France; INSERM U661, F-34000 Montpellier, France; Universités de Montpellier 1 and 2, F-34000 Montpellier, France.
CNRS UMR 5203, Institut de Génomique Fonctionnelle, F-34000 Montpellier, France; INSERM U661, F-34000 Montpellier, France; Universités de Montpellier 1 and 2, F-34000 Montpellier, France.
Pharmacol Res. 2014 May;83:74-8. doi: 10.1016/j.phrs.2013.10.007. Epub 2013 Nov 13.
Conformational diseases result from protein misfolding and/or aggregation and constitute a major public health problem. Congenital Nephrogenic Diabetes Insipidus is a typical conformational disease. In most of the cases, it is associated to inactivating mutations of the renal arginine-vasopressin V2 receptor gene leading to misfolding and intracellular retention of the receptor, causing the inability of patients to concentrate their urine in response to the antidiuretic hormone. Cell-permeable pharmacological chaperones have been successfully challenged to restore plasma membrane localization of the receptor mutants and to rescue their function. Interestingly, different classes of specific ligands such as antagonists (vaptans), agonists as well as biased agonists of the V2 receptor have proven their usefulness as efficient pharmacochaperones. These compounds represent a potential therapeutic treatment of this X-linked genetic pathology.
构象疾病由蛋白质错误折叠和/或聚集引起,是一个重大的公共卫生问题。先天性肾性尿崩症是一种典型的构象疾病。在大多数情况下,它与肾血管加压素V2受体基因的失活突变有关,导致受体错误折叠并滞留于细胞内,使患者无法在抗利尿激素作用下浓缩尿液。细胞渗透性药理伴侣已成功用于恢复受体突变体的质膜定位并挽救其功能。有趣的是,不同类别的特异性配体,如拮抗剂(血管加压素受体拮抗剂)、激动剂以及V2受体的偏向激动剂,已证明它们作为有效药理伴侣的有效性。这些化合物代表了这种X连锁遗传疾病的一种潜在治疗方法。