Suppr超能文献

降钙素抑制大鼠垂体GGH3细胞中催乳素启动子活性:p42/44丝裂原活化蛋白激酶参与降钙素作用的证据。

Calcitonin inhibits prolactin promoter activity in rat pituitary GGH3 cells: evidence for involvement of p42/44 mitogen-activated protein kinase in calcitonin action.

作者信息

Ren Yuan, Sun Ya-Ping, Shah Girish V

机构信息

Department of Pharmceutical Sciences, Texas Tech University Health Science Center, Amarillo, TX 79109, USA.

出版信息

Endocrine. 2003 Feb-Mar;20(1-2):13-22. doi: 10.1385/ENDO:20:1-2:13.

Abstract

Previous findings from our laboratory have shown that pituitary calcitonin-like peptide (pit-CT) is synthesized and released by gonadotrophs and inhibits prolactin (PRL) release, synthesis, and lactotroph proliferation. To investigate further the regulation of PRL gene transcription by CT, we examined the effect of CT on rat PRL (rPRL) promoter activity in rat pituitary GGH3 cells. GGH3 cells were transiently transfected with rPRL promoter- luciferase and control plasmids. Thirty-six hours later, the cells were treated with CT or other agents and their effect on luciferase activity was examined. The effect of CT and/or thyrotropin-releasing hormone (TRH) on p42/44 mitogen-activated protein kinase (MAPK) activity was also investigated. CT inhibited basal rPRL promoter activity in a dose-dependent fashion, with an approximate IC(50) of 3 nM. The maximal inhibition occurred 1 h after the CT addition, and the peptide was equipotent in inhibiting 600 and 2500 rPRL promoter constructs. CT also inhibited TRH-, Bay K 8644-, and ionomycin-induced rPRL promoter activity. CT mimicked the actions of MEK inhibitors U0126 and PD 980089. However, CT could not inhibit rPRL promoter activity in GGH3 cells expressing constitutively active ERK1 or ERK2. CT markedly attenuated phospho-MAPK immunoreactivity in untreated as well as TRH-treated GGH3 cells. These results suggest that CT inhibits rPRL promoter activity by antagonizing Ca(2+) and ERK1/2-mediated signaling events. They also demonstrate that CT is a potent inhibitor of early events associated with PRL gene activation and may play an important role in regulation of lactotroph function.

摘要

我们实验室先前的研究结果表明,垂体降钙素样肽(pit-CT)由促性腺激素细胞合成并释放,可抑制催乳素(PRL)的释放、合成及催乳素细胞增殖。为进一步研究降钙素(CT)对PRL基因转录的调控作用,我们检测了CT对大鼠垂体GGH3细胞中大鼠PRL(rPRL)启动子活性的影响。将rPRL启动子-荧光素酶质粒和对照质粒瞬时转染至GGH3细胞。36小时后,用CT或其他试剂处理细胞,并检测其对荧光素酶活性的影响。同时还研究了CT和/或促甲状腺激素释放激素(TRH)对p42/44丝裂原活化蛋白激酶(MAPK)活性的影响。CT以剂量依赖方式抑制基础rPRL启动子活性,其半数抑制浓度(IC50)约为3 nM。最大抑制作用在添加CT后1小时出现,该肽对抑制600和2500 rPRL启动子构建体的效果相同。CT还抑制TRH-、Bay K 8644-和离子霉素诱导的rPRL启动子活性。CT模拟了MEK抑制剂U012,6和PD 98059的作用。然而,CT不能抑制组成型激活的ERK1或ERK2表达的GGH3细胞中的rPRL启动子活性。CT显著减弱了未处理以及TRH处理的GGH3细胞中的磷酸化MAPK免疫反应性。这些结果表明,CT通过拮抗Ca(2+)和ERK1/2介导的信号事件来抑制rPRL启动子活性。它们还表明,CT是与PRL基因激活相关的早期事件的有效抑制剂,可能在催乳素细胞功能的调节中起重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验