首页> 外文期刊>Regulatory peptides. >Role of CREB in vasoactive intestinal peptide-mediated wound healing in human bronchial epithelial cells.
【24h】

Role of CREB in vasoactive intestinal peptide-mediated wound healing in human bronchial epithelial cells.

机译:CREB在人支气管上皮细胞中血管活性肠肽介导的伤口愈合中的作用。

获取原文
获取原文并翻译 | 示例
           

摘要

Vasoactive intestinal peptide (VIP) is one of the most important sensory neuropeptides in respiratory system. We previously reported that VIP enhances wound healing and proliferation of human bronchial epithelial cells (HBECs), and these effects are mediated by intracellular signaling molecules such as protein kinase A (PKA), protein kinase C (PKC), Calmodulin (CaM), and extracellular signal-regulated kinase (ERK). In the present study, we further investigated the role of cAMP Response Element Binding Protein (CREB) in VIP-promoted protective effects in mechanical-damaged HBECs. VIP-mediated wound healing and cell proliferation in HBECs was inhibited by CREB antisense oligonucleotides (ASO) in a time-dependent manner. VIP increased the CREB DNA binding activity and expression of the p-CREB that were inhibited by VIP receptor antagonist. Increased CREB DNA binding activity and expression of the p-CREB were also partially inhibited by PKA and ERK inhibitors. These results suggest that the VIP-mediated wound repair of HBECs is associated with activation of CREB via PKA and ERK dependent pathway.
机译:血管活性肠肽(VIP)是呼吸系统中最重要的感觉神经肽之一。我们先前曾报道VIP增强了人类支气管上皮细胞(HBEC)的伤口愈合和增殖,并且这些作用是由细胞内信号分子介导的,例如蛋白激酶A(PKA),蛋白激酶C(PKC),钙调蛋白(CaM)和细胞外信号调节激酶(ERK)。在本研究中,我们进一步研究了cAMP反应元件结合蛋白(CREB)在VIP促进的机械损伤HBEC保护作用中的作用。 CREB反义寡核苷酸(ASO)以时间依赖性方式抑制HBEC中VIP介导的伤口愈合和细胞增殖。 VIP增加了VIP受体拮抗剂抑制的CREB ​​DNA结合活性和p-CREB的表达。增加的CREB ​​DNA结合活性和p-CREB的表达也被PKA和ERK抑制剂部分抑制。这些结果表明,VIP介导的HBEC伤口修复与通过PKA和ERK依赖性途径激活CREB有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号