Allinson E T, Drucker D J
Department of Clinical Biochemistry, University of Toronto, Ontario, Canada.
Cancer Res. 1992 Jun 1;52(11):3103-9.
The parathyroid hormone-like peptide (PLP) gene is widely expressed in normal and neoplastic tissues. Previous studies have demonstrated that PLP gene expression is regulated by serum and cycloheximide, features common to the regulation of a number of different early response genes. We now report that PLP mRNA transcripts are induced within 5 min of exposure of rat keratinocytes to serum, return to control values at 20 min, and then increase and remain elevated for at least 4 h, following which they return to baseline levels. The PLP mRNA t1/2 was approximately 90 min in both serum-deprived and serum-stimulated cells. The serum induction was blocked by actinomycin D. Cycloheximide alone induced PLP gene expression; however, PLP mRNA transcripts were not superinduced in the presence of both serum and cycloheximide. Dexamethasone and 1,25-dihydroxyvitamin D3 inhibited the basal levels of PLP mRNA transcripts but did not eliminate the serum induction of PLP gene expression. Epidermal growth factor or transforming growth factor-beta alone induced PLP mRNA transcripts, but no induction was observed following exposure of cells to epidermal growth factor and transforming growth factor-beta together. Treatment with 12-O-tetradecanoylphorbol-13-acetate for 90 min did not induce PLP mRNA transcripts, but 12-O-tetradecanoylphorbol-13-acetate blocked the rapid serum induction of PLP gene expression. These features of PLP gene expression suggest that PLP is a member of the growth factor-regulated early response gene family. The rapid serum stimulation of PLP gene expression raises the possibility that PLP may contribute in an autocrine fashion to the early cellular response to growth factor stimulation.
甲状旁腺激素样肽(PLP)基因在正常组织和肿瘤组织中广泛表达。先前的研究表明,PLP基因表达受血清和环己酰亚胺调节,这是许多不同早期反应基因调节的共同特征。我们现在报告,大鼠角质形成细胞暴露于血清后5分钟内PLP mRNA转录本被诱导,20分钟时恢复到对照值,然后升高并至少维持4小时,之后恢复到基线水平。在血清剥夺和血清刺激的细胞中,PLP mRNA的半衰期约为90分钟。放线菌素D可阻断血清诱导。单独使用环己酰亚胺可诱导PLP基因表达;然而,在同时存在血清和环己酰亚胺的情况下,PLP mRNA转录本并未超诱导。地塞米松和1,25-二羟基维生素D3抑制PLP mRNA转录本的基础水平,但并未消除血清对PLP基因表达的诱导。单独的表皮生长因子或转化生长因子-β可诱导PLP mRNA转录本,但细胞同时暴露于表皮生长因子和转化生长因子-β后未观察到诱导作用。用12-O-十四烷酰佛波醇-13-乙酸酯处理90分钟未诱导PLP mRNA转录本,但12-O-十四烷酰佛波醇-13-乙酸酯可阻断血清对PLP基因表达的快速诱导。PLP基因表达的这些特征表明PLP是生长因子调节的早期反应基因家族的成员。血清对PLP基因表达的快速刺激增加了PLP可能以自分泌方式参与细胞对生长因子刺激的早期反应的可能性。