Heinrich G, Kronenberg H M, Potts J T, Habener J F
Endocrinology. 1983 Feb;112(2):449-58. doi: 10.1210/endo-112-2-449.
The effects of changes in the concentration of extracellular calcium the principal regulatory of PTH secretion, on the cellular levels of the mRNA encoding prepro-PTH, a precursor of PTH, were studied in bovine parathyroid slices in vitro using a sensitive radiodensitometric cDNA hybridization assay and mRNA translation in a wheat germ cell-free system. Although lowering the calcium from 5 to 0.5 mM during 5- to 70-h incubations stimulated the secretion of PTH 4- to 8-fold and pro-PTH synthesis 1.4-fold, the cellular levels of total hybridizable PTH mRNA did not change. However, a 2- to 3-fold increase in PTH mRNA, which could be hybridized to oligo-dT-cellulose [poly(A)-rich], was observed in the slices incubated in 5 mM calcium (suppressed slices). The poly(A)-rich PTH mRNA constituted 30% of the total PTH mRNA in suppressed gland slices and 10% of the total PTH mRNA in stimulated gland slices. PTH mRNA did not decay measurably when RNA synthesis in the gland slices was inhibited with actinomycin D and alpha-amanitin for 6 h. Both the stability and the lack of perturbation of the cellular levels of total of total hybridizable PTH mRNA by changes in the concentration of extracellular calcium suggest that the short term regulation of PTH biosynthesis involves posttranscriptional mechanisms.
细胞外钙浓度变化(甲状旁腺激素分泌的主要调节因素)对甲状旁腺激素前体——前甲状旁腺激素原编码mRNA的细胞水平的影响,采用灵敏的放射密度测定cDNA杂交分析法和麦胚无细胞系统中的mRNA翻译法,在体外牛甲状旁腺切片中进行了研究。虽然在5至70小时的孵育过程中将钙浓度从5 mM降至0.5 mM会刺激甲状旁腺激素分泌增加4至8倍,前甲状旁腺激素合成增加1.4倍,但可杂交的甲状旁腺激素mRNA的细胞水平并未改变。然而,在5 mM钙(抑制切片)中孵育的切片中,观察到可与寡聚dT纤维素[富含多聚(A)]杂交的甲状旁腺激素mRNA增加了2至3倍。富含多聚(A)的甲状旁腺激素mRNA在抑制腺体切片中占总甲状旁腺激素mRNA的30%,在刺激腺体切片中占总甲状旁腺激素mRNA的10%。当用放线菌素D和α-鹅膏蕈碱抑制腺体切片中的RNA合成6小时时,甲状旁腺激素mRNA没有明显降解。细胞外钙浓度变化对可杂交的甲状旁腺激素mRNA总细胞水平的稳定性和无干扰表明,甲状旁腺激素生物合成的短期调节涉及转录后机制。