Wu Xiang, Shen Hong, Yu Ling, Peng Mei, Lai Wei-Si, Ding Yi-Ling
Dept. of Gynecology and Obstetrics, The Second Xiangya Hospital, Central South Univ., Changsha, Hunan 410011, China.
Am J Physiol Endocrinol Metab. 2007 Dec;293(6):E1789-94. doi: 10.1152/ajpendo.00249.2007. Epub 2007 Sep 25.
Corticotropin-releasing hormone (CRH) and connexin 43 (Cx43) play crucial roles in uterine contraction and the onset of labor. The aim of the present study was to investigate the regulatory effects of CRH on Cx43 expression in human myometrial smooth muscle cells (SMCs) and, potentially, its activation of the c-Fos/activator protein (AP)-1 signaling pathway. Human myometrial SMCs collected from nonpregnant women were treated with different concentrations of CRH. Transient transfection of AP-1 decoy oligodeoxynucleotide (ODN) was used to block AP-1 sites of Cx43. The transcriptional activity of AP-1 was detected by luciferase assay. Cx43 protein expression was visualized by immunofluorescence staining. mRNA and protein expression of c-Fos and Cx43 were demonstrated by real-time quantitative RT-PCR and Western blot, respectively. CRH facilitated Cx43 expression and enhanced AP-1 promoter activity in human uterine SMCs. After CRH treatment, Cx43 expression in the cytoplasm increased significantly. CRH significantly increased mRNA and protein expression of c-Fos and Cx43 in a dose-dependent manner (P < 0.01). A transient transfection of AP-1 decoy ODN did not affect CRH regulation of c-Fos (P > 0.05) but almost completely abolished CRH-induced enhancement of Cx43 expression (P < 0.01). In human primary myometrial SMCs, CRH enhances Cx43 mRNA and protein expression through upregulation of c-Fos expression. Blockade of AP-1 sites to the Cx43 promoter can neutralize the CRH-induced upregulation of Cx43.
促肾上腺皮质激素释放激素(CRH)和连接蛋白43(Cx43)在子宫收缩和分娩发动中起关键作用。本研究的目的是探讨CRH对人子宫肌层平滑肌细胞(SMC)中Cx43表达的调节作用,以及其对c-Fos/激活蛋白(AP)-1信号通路的激活作用。用不同浓度的CRH处理从非孕妇收集的人子宫肌层SMC。采用AP-1诱饵寡脱氧核苷酸(ODN)瞬时转染来阻断Cx43的AP-1位点。通过荧光素酶测定检测AP-1的转录活性。通过免疫荧光染色观察Cx43蛋白表达。分别通过实时定量RT-PCR和蛋白质印迹法检测c-Fos和Cx43的mRNA和蛋白表达。CRH促进人子宫SMC中Cx43表达并增强AP-1启动子活性。CRH处理后,细胞质中Cx43表达显著增加。CRH以剂量依赖性方式显著增加c-Fos和Cx43的mRNA和蛋白表达(P<0.01)。AP-1诱饵ODN瞬时转染不影响CRH对c-Fos的调节(P>0.05),但几乎完全消除了CRH诱导的Cx43表达增强(P<0.01)。在人原代子宫肌层SMC中,CRH通过上调c-Fos表达增强Cx43 mRNA和蛋白表达。阻断Cx43启动子的AP-1位点可中和CRH诱导的Cx43上调。