Roussanne M C, Gogusev J, Hory B, Duchambon P, Souberbielle J C, Nabarra B, Pierrat D, Sarfati E, Drüeke T, Bourdeau A
Unité 90 INSERM and Département de Néphrologie, Hôpital Necker, Paris, France.
J Bone Miner Res. 1998 Mar;13(3):354-62. doi: 10.1359/jbmr.1998.13.3.354.
An original human parathyroid cell culture model from uremic patients with IIo hyperparathyroidism has been developed, with its main feature being long-term functionally active viability up to 5 months, as assessed by persistent responsiveness to changes of extracellular Ca2+ concentrations ([Ca2+]e). In addition to the inhibitory effect of increasing [Ca2+]e, increasing extracellular phosphate exerted a biphasic effect on parathyroid hormone (PTH) secretion. The presence of the Ca2+-sensing receptor (CaR), on which depends the response to [Ca2+]e and its persistence, has been demonstrated in our culture system both by direct detection and by inhibition of its activity. CaR protein was detected by Western blot analysis with a specific anti-CaR antibody. CaR gene transcripts have been identified by reverse transcription-polymerase chain reaction analysis. mRNA (by in situ hybridization) and protein (by immunocytochemistry) expression were detected for both CaR and PTH. Adding a specific anti-CaR antibody to the medium induced a marked reduction of low [Ca2+]e-stimulated PTH release, which decreased to levels equivalent to those obtained in high [Ca2+]e medium. The described long-term functionality could be due to several factors, including the clustered cell type of culture yielded by our preparation procedure, the growth characteristics of hyperplastic uremic tissue, and the use of a phosphate-rich medium. The present model, because of its long-term functionality, is a unique tool for the exploration of PTH synthesis and secretion and for studies of parathyroid cell growth in vitro.
已建立了一种来自患有继发性甲状旁腺功能亢进的尿毒症患者的原代人甲状旁腺细胞培养模型,其主要特征是通过对细胞外Ca2+浓度([Ca2+]e)变化的持续反应性评估,具有长达5个月的长期功能活性生存能力。除了增加[Ca2+]e的抑制作用外,增加细胞外磷酸盐对甲状旁腺激素(PTH)分泌产生双相作用。通过直接检测及其活性抑制,在我们的培养系统中已证实存在Ca2+敏感受体(CaR),对[Ca2+]e的反应及其持续性取决于该受体。用特异性抗CaR抗体通过蛋白质印迹分析检测CaR蛋白。通过逆转录-聚合酶链反应分析鉴定CaR基因转录本。通过原位杂交检测CaR和PTH的mRNA表达,通过免疫细胞化学检测蛋白质表达。向培养基中添加特异性抗CaR抗体可导致低[Ca2+]e刺激的PTH释放显著减少,降至与高[Ca2+]e培养基中获得的水平相当的水平。所描述的长期功能可能归因于几个因素,包括我们的制备程序产生的培养细胞簇类型、增生性尿毒症组织的生长特性以及使用富含磷酸盐的培养基。由于其长期功能,本模型是探索PTH合成和分泌以及体外甲状旁腺细胞生长研究的独特工具。