Russell J, Zhao W, Christ G, Ashok S, Angeletti R H
Department of Medicine, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Mol Cell Biol Res Commun. 1999 Jun;1(3):221-6. doi: 10.1006/mcbr.1999.0135.
It has been well established that increases in extracellular calcium concentration ([Ca2+]) inhibit parathyroid hormone (PTH) secretion. The effects of [Ca2+] are mediated through a G-protein-coupled receptor that has been cloned and characterized. Additionally, it has been demonstrated in parathyroid cells that an increase in [Ca2+] results in an increase in steady-state levels of intracellular calcium ([Ca2+]i). At present, it has not been fully resolved whether changes in [Ca2+]i are related to changes in PTH secretion. In the current study, the effect of increased [Ca2+] on PTH secretion and the connection regarding changes in concentrations of intracellular calcium [Ca2+]i have been examined in primary cultures of bovine parathyroid cells. PTH secretion was measured by radioimmunoassay and intracellular calcium was determined by single cell calcium imaging. Bovine parathyroid cells pre-incubated with either 0.5 or 1 mM calcium responded to rapid increases in [Ca2+] (> or = 0.5 mM) with an immediate and sustained increase in steady-state levels of [Ca2+]i that persisted for time intervals greater than 15 minutes. Although the magnitude of the sustained increase in [Ca2+]i varied among individual cells (approximately 40% to > 300%), the overall pattern and course of time were similar in all cells examined (n = 142). In all trials, [Ca2+]i immediately returned to baseline levels following the addition of the calcium chelator, 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (BAPTA). Additional control studies, however, suggest that sustained increases in [Ca2+]i do not correlate with regulation of parathyroid hormone secretion. Sustained elevations of [Ca2+]i were not observed when [Ca2+] was gradually increased by the addition of 0.1 mM increments at 1 minute intervals. Furthermore, the effect on inhibition of PTH secretion was the same regardless of whether [Ca2+] was increased by gradual or rapid addition.
细胞外钙浓度([Ca2+])升高会抑制甲状旁腺激素(PTH)分泌,这一点已经得到充分证实。[Ca2+]的作用是通过一种已被克隆和鉴定的G蛋白偶联受体介导的。此外,在甲状旁腺细胞中已经证实,[Ca2+]升高会导致细胞内钙([Ca2+]i)的稳态水平升高。目前,[Ca2+]i的变化是否与PTH分泌的变化相关尚未完全明确。在本研究中,在牛甲状旁腺细胞原代培养物中检测了[Ca2+]升高对PTH分泌的影响以及与细胞内钙浓度[Ca2+]i变化的关联。通过放射免疫测定法测量PTH分泌,通过单细胞钙成像测定细胞内钙。预先用0.5或1 mM钙孵育的牛甲状旁腺细胞对[Ca2+]的快速升高(≥0.5 mM)作出反应,[Ca2+]i的稳态水平立即且持续升高,持续时间超过15分钟。尽管[Ca2+]i持续升高的幅度在各个细胞之间有所不同(约40%至>300%),但在所检查的所有细胞(n = 142)中,总体模式和时间进程相似。在所有试验中,加入钙螯合剂1,2-双(2-氨基苯氧基)乙烷-N,N,N',N'-四乙酸(BAPTA)后,[Ca2+]i立即恢复到基线水平。然而,额外的对照研究表明,[Ca2+]i的持续升高与甲状旁腺激素分泌的调节无关。当以1分钟间隔逐次添加0.1 mM使[Ca2+]逐渐升高时,未观察到[Ca2+]i的持续升高。此外,无论[Ca2+]是通过逐渐添加还是快速添加而升高,对PTH分泌抑制的效果都是相同的。