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地塞米松与钙在甲状旁腺细胞中甲状旁腺激素和嗜铬粒蛋白A分泌及信使核糖核酸水平的调节中相互作用。

Dexamethasone and calcium interact in the regulation of parathormone and chromogranin-A secretion and messenger ribonucleic acid levels in parathyroid cells.

作者信息

Zhang J X, Fasciotto B H, Cohn D V

机构信息

Department of Biological and Biophysical Sciences, University of Louisville Health Sciences Center, Kentucky 40292.

出版信息

Endocrinology. 1993 Jul;133(1):152-8. doi: 10.1210/endo.133.1.8319562.

Abstract

We investigated the interaction of dexamethasone and Ca2+ on the secretion of PTH and chromogranin-A (CgA) by porcine parathyroid cells in culture and on the cellular levels of PTH and CgA mRNA. Freshly dispersed parathyroid cells were cultured for 6 days in Ham's F-12 medium containing 10% fetal calf serum and 1 mM Ca2+. The experiments were initiated at 0.5 or 3.0 mM Ca2+ in 0.5% serum with or without dexamethasone for an additional 24 or 48 h. Secretion of PTH and CgA was 50-60% less, and the respective mRNAs levels were about 75% lower at 3.0 than at 0.5 mM Ca2+. Dexamethasone (10(-9)-10(-7) M) stimulated the secretion of PTH in a dose-dependent fashion about 2-fold at both 3.0 and 0.5 mM Ca2+ and increased the PTH mRNA level 15-fold at the high and 3-fold at the low Ca2+ concentration. In contrast, the direction of action of dexamethasone on the secretion of CgA and CgA mRNA was dependent upon the Ca2+ concentration. At 3.0 mM Ca2+, dexamethasone increased CgA secretion and mRNA levels about 2- and 8-fold, respectively. In contrast, at 0.5 mM Ca2+ dexamethasone decreased CgA secretion to one half and its mRNA to one tenth that cells without the glucocorticoid. The stimulatory action of dexamethasone on PTH and CgA mRNA could be noted in 12 h or less and continued through 24-48 h. These results demonstrate a decoupling of PTH and CgA secretion and gene regulation. Our data accord with a role for CgA as an autocrine regulator of parathyroid gland secretion.

摘要

我们研究了地塞米松和钙离子(Ca2+)对培养的猪甲状旁腺细胞甲状旁腺激素(PTH)和嗜铬粒蛋白A(CgA)分泌以及PTH和CgA mRNA细胞水平的相互作用。将新鲜分散的甲状旁腺细胞在含有10%胎牛血清和1 mM Ca2+的Ham's F-12培养基中培养6天。实验在含0.5%血清、0.5或3.0 mM Ca2+且有或无地塞米松的条件下再进行24或48小时。在3.0 mM Ca2+时,PTH和CgA的分泌减少50 - 60%,各自的mRNA水平比0.5 mM Ca2+时低约75%。地塞米松(10(-9) - 10(-7) M)以剂量依赖方式刺激PTH分泌,在3.0和0.5 mM Ca2+时均约为2倍,并在高钙浓度下使PTH mRNA水平增加15倍,在低钙浓度下增加3倍。相反,地塞米松对CgA分泌和CgA mRNA的作用方向取决于Ca2+浓度。在3.0 mM Ca2+时地塞米松使CgA分泌和mRNA水平分别增加约2倍和8倍。相比之下,在0.5 mM Ca2+时,地塞米松使CgA分泌降至无糖皮质激素细胞的一半,其mRNA降至十分之一。地塞米松对PTH和CgA mRNA的刺激作用在12小时或更短时间内即可观察到,并持续24 - 48小时。这些结果表明PTH和CgA分泌及基因调控存在解偶联。我们的数据符合CgA作为甲状旁腺分泌自分泌调节因子的作用。

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