Symes A J, Pitts R L, Conover J, Kos K, Coulombe J
Department of Pharmacology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814, USA.
Mol Endocrinol. 2000 Mar;14(3):429-39. doi: 10.1210/mend.14.3.0429.
Activin, a member of the transforming growth factor-beta superfamily, can regulate neuropeptide gene expression in the nervous system and in neuroblastoma cells. Among the neuropeptide genes whose expression can be regulated by activin is the gene encoding the neuropeptide vasoactive intestinal peptide (VIP). To investigate the molecular mechanisms by which activin regulates neuronal gene expression, we have examined activin's regulation of VIP gene expression in NBFL neuroblastoma cells. We report here that NBFL cells respond to activin by increasing expression of VIP mRNA. Activin regulates VIP gene transcription in NBFL cells through a 180-bp element in the VIP promoter that was previously characterized to be necessary and sufficient to mediate the induction of VIP by the neuropoietic cytokines and termed the cytokine response element (CyRE). We find that the VIP CyRE is necessary and sufficient to mediate the transcriptional response to activin. In addition, ciliary neurotrophic factor (CNTF), a neuropoietic cytokine, synergizes with activin to increase VIP mRNA expression and transcription through the VIP CyRE. Mutations in either the Stat (signal transducer and activator of transcription) or AP-1 sites within the CyRE that reduce the response to CNTF, also reduce the response to activin. However, mutating both the Stat and AP-1 sites within the wild-type CyRE, while reducing the separate responses to either activin or CNTF, eliminates the synergy between them. These data suggest that activin and CNTF, two factors that appear to signal though distinct pathways, activate VIP gene transcription through a common transcriptional element, the VIP CyRE.
激活素是转化生长因子-β超家族的成员之一,可调节神经系统和神经母细胞瘤细胞中神经肽基因的表达。其表达可受激活素调节的神经肽基因中,包括编码神经肽血管活性肠肽(VIP)的基因。为了研究激活素调节神经元基因表达的分子机制,我们检测了激活素对NBFL神经母细胞瘤细胞中VIP基因表达的调节作用。我们在此报告,NBFL细胞对激活素的反应是增加VIP mRNA的表达。激活素通过VIP启动子中的一个180 bp元件调节NBFL细胞中的VIP基因转录,该元件先前已被鉴定为介导神经生成细胞因子诱导VIP所必需且充分的元件,称为细胞因子反应元件(CyRE)。我们发现VIP CyRE对于介导对激活素的转录反应是必需且充分的。此外,神经生成细胞因子睫状神经营养因子(CNTF)与激活素协同作用,通过VIP CyRE增加VIP mRNA的表达和转录。CyRE内Stat(信号转导子和转录激活子)或AP-1位点的突变会降低对CNTF的反应,同时也会降低对激活素的反应。然而,在野生型CyRE内同时突变Stat和AP-1位点,虽然会降低对激活素或CNTF的单独反应,但会消除它们之间的协同作用。这些数据表明,激活素和CNTF这两种似乎通过不同途径发出信号的因子,通过一个共同的转录元件VIP CyRE激活VIP基因转录。