De Luca F, Ray K, Mancilla E E, Fan G F, Winer K K, Gore P, Spiegel A M, Baron J
Developmental Endocrinology Branch, National Institute of Child Health and Human Development Bethesda, Maryland 20892, USA.
J Clin Endocrinol Metab. 1997 Aug;82(8):2710-5. doi: 10.1210/jcem.82.8.4166.
Activating mutations of the Ca(2+)-sensing receptor (CaR) gene have been identified in families with autosomal dominant hypoparathyroidism and in one patient with sporadic hypoparathyroidism. Here, we describe two additional patients with sporadic hypoparathyroidism. One patient presented with mild symptoms at age 18 yr; the other was severely symptomatic from infancy. A heterozygous missense mutation was identified in each patient. One mutation (L773R) involved the fifth transmembrane domain of the CaR, the other (N118K) affected the amino-terminal, extracellular domain. In both cases, the probands' parents lacked the mutation, indicating that the mutations arose de novo. In expression studies the mutations shifted the concentration-response curve to the left and increased maximal activity. We conclude that 1) sporadic hypoparathyroidism can be caused by de novo gain-of-function mutations of the CaR; 2) the phenotype can vary from mild to life-threatening hypocalcemia; 3) gain-of-function mutations can involve not only extracellular regions, as previously reported, but also transmembrane domains of the CaR; and 4) the mechanism of activation can involve both increased receptor sensitivity to Ca2+ and increased maximal signal transduction.
在常染色体显性遗传性甲状旁腺功能减退症家族以及一名散发性甲状旁腺功能减退症患者中,已发现钙敏感受体(CaR)基因的激活突变。在此,我们描述另外两名散发性甲状旁腺功能减退症患者。一名患者18岁时出现轻微症状;另一名从婴儿期起就有严重症状。在每名患者中均鉴定出一个杂合错义突变。一个突变(L773R)涉及CaR的第五个跨膜结构域,另一个(N118K)影响氨基末端的细胞外结构域。在这两个病例中,先证者的父母均无此突变,表明这些突变是新发的。在表达研究中,这些突变使浓度-反应曲线向左移动并增加了最大活性。我们得出结论:1)散发性甲状旁腺功能减退症可由CaR的新发功能获得性突变引起;2)表型可从轻度到危及生命的低钙血症不等;3)功能获得性突变不仅可累及如先前报道的细胞外区域,还可累及CaR的跨膜结构域;4)激活机制可涉及受体对Ca2+敏感性增加以及最大信号转导增加。