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培养的甲状旁腺组织中钙对甲状旁腺激素信使核糖核酸的调节作用。

Regulation by calcium of parathyroid hormone mRNA in cultured parathyroid tissue.

作者信息

Brookman J J, Farrow S M, Nicholson L, O'Riordan J L, Hendy G N

机构信息

Department of Medicine, Middlesex Hospital, London, U.K.

出版信息

J Bone Miner Res. 1986 Dec;1(6):529-37. doi: 10.1002/jbmr.5650010607.

Abstract

We have examined the effect of changes in the concentration of extracellular calcium on parathyroid hormone mRNA in both short-term (hours) and long-term (days) cultures of bovine parathyroid tissue. Using a 32P-labeled PreProPTH cDNA probe, PTH mRNA was measured by gel blot hybridization of total RNA from tissue slices incubated for 4 h in low (0.5 mM) or high (5 mM) calcium concentrations and also by dot blot hybridization of cytoplasmic RNA extracted from aggregates of partially dispersed cells cultured up to 72 h in low (0.4 mM), normal (1 mM), or high (3 mM) calcium concentrations. PTH mRNA was unchanged over 4 h while high calcium had suppressed PTH secretion. However PTH mRNA did respond during long-term culture. By 24 h in high calcium there was a 50% suppression which was maintained for a further 48 h. PTH mRNA in normal calcium remained unchanged over 72 h while in low calcium it had increased slightly by 48 h. In contrast to the effect seen in cultured bovine parathyroid cells, PTH mRNA in human parathyroid adenoma cells cultured for 48 h in high calcium was decreased by only 10%.

摘要

我们研究了细胞外钙浓度变化对牛甲状旁腺组织短期(数小时)和长期(数天)培养中甲状旁腺激素mRNA的影响。使用32P标记的前甲状旁腺素原cDNA探针,通过对在低钙(0.5 mM)或高钙(5 mM)浓度下孵育4小时的组织切片的总RNA进行凝胶印迹杂交,以及对在低钙(0.4 mM)、正常钙(1 mM)或高钙(3 mM)浓度下培养长达72小时的部分分散细胞聚集体中提取的细胞质RNA进行斑点印迹杂交来测量甲状旁腺激素mRNA。在4小时内甲状旁腺激素mRNA没有变化,而高钙抑制了甲状旁腺激素的分泌。然而,在长期培养过程中甲状旁腺激素mRNA确实有反应。在高钙环境中培养24小时后,其水平受到50%的抑制,并在接下来的48小时内保持这一水平。正常钙浓度下的甲状旁腺激素mRNA在72小时内保持不变,而在低钙环境中,到48小时时略有增加。与培养的牛甲状旁腺细胞中观察到的效应相反,在高钙环境中培养48小时的人甲状旁腺腺瘤细胞中的甲状旁腺激素mRNA仅下降了10%。

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