Metabolism and Systems Science and Centre for Diabetes, Endocrinology and Metabolism (CEDAM), University of Birmingham, Birmingham, UK.
Centre for Membrane Proteins and Receptors (COMPARE), Universities of Birmingham and Nottingham, Birmingham, UK.
Methods Mol Biol. 2025;2861:43-55. doi: 10.1007/978-1-0716-4164-4_4.
The calcium-sensing receptor (CaSR) has a critical role in maintaining serum calcium concentrations within the normal physiological range, and mutations in the receptor, or components of its signaling and trafficking pathway, cause disorders of calcium homeostasis. Inactivating mutations cause neonatal severe hyperparathyroidism or familial hypocalciuric hypercalcemia (FHH), while gain-of-function mutations cause autosomal dominant hypocalcemia (ADH). Characterizing the functional impact of mutations of the CaSR, and components of the CaSR-signaling pathway, is clinically important to enable correct diagnoses of FHH and ADH, optimize management, and prevent inappropriate parathyroidectomy or vitamin D supplementation. CaSR signals predominantly by activating the G-alpha subunit-11 to mobilize calcium release from intracellular stores. Thus, measurement of CaSR-induced intracellular calcium (Ca) signaling is the gold standard method to investigate the pathogenicity of CaSR genetic variants. This protocol describes a method to assess CaSR-induced Ca signaling using the Indo-1 calcium indicator dye and flow cytometry. This method has been used to assess multiple genetic variants in CaSR and components of its signaling and trafficking pathway in HEK293 cells.
钙敏感受体 (CaSR) 在维持血清钙浓度在正常生理范围内发挥着关键作用,而受体或其信号转导和运输途径的成分中的突变会导致钙稳态紊乱。失活突变会导致新生儿严重甲状旁腺功能亢进或家族性低钙血症性高钙血症 (FHH),而功能获得性突变会导致常染色体显性低钙血症 (ADH)。鉴定 CaSR 及其信号转导途径成分的突变对正确诊断 FHH 和 ADH、优化管理以及防止不适当的甲状旁腺切除术或维生素 D 补充至关重要。CaSR 主要通过激活 G-α亚基-11 来激活细胞内储存的钙释放来发挥作用。因此,测量 CaSR 诱导的细胞内钙 (Ca) 信号是研究 CaSR 遗传变异致病性的金标准方法。该方案描述了一种使用 Indo-1 钙指示剂染料和流式细胞术评估 CaSR 诱导的 Ca 信号的方法。该方法已用于评估 HEK293 细胞中的 CaSR 及其信号转导和运输途径的多个遗传变异。