Breuer W, Kartner N, Riordan J R, Cabantchik Z I
Department of Biological Chemistry, Hebrew University of Jerusalem, Israel.
J Biol Chem. 1992 May 25;267(15):10465-9.
The cystic fibrosis transmembrane conductance regulator (CFTR) was studied in HT-29 human colonic carcinoma cells with the aim of assessing possible mechanisms of up-regulation of its expression. CFTR was identified and quantified in total cell extracts by Western immunoblots using a monoclonal anti-CFTR antibody and was functionally assessed by tracer Cl-efflux from intact cells. It was found that various stimuli that lead to a sustained (greater than or equal to 8 h) elevation of intracellular cyclic AMP elicited a marked and specific increase in CFTR expression in cell membranes and concomitant activation of Cl- secretion. Further activation of Cl- secretion was obtained by additional short term activation by cyclic AMP analogues or cyclic AMP-inducing agents. Blockers of transcription or translation largely depressed the cAMP-mediated induction of CFTR levels and associated function, indicating that the inductive phenomenon was at the transcriptional level. The results imply the involvement of putative cyclic AMP responsive (and related) elements that are present in the CFTR gene promoter and that are known to modulate eukaryotic gene expression. Activation of these elements by various stimuli might provide pharmacological tools for up-regulation of CFTR expression at both biochemical and physiological levels.
在HT - 29人结肠癌细胞中对囊性纤维化跨膜传导调节因子(CFTR)进行了研究,目的是评估其表达上调的可能机制。通过使用单克隆抗CFTR抗体的Western免疫印迹法在总细胞提取物中鉴定并定量CFTR,并通过完整细胞的示踪剂Cl-外流对其功能进行评估。发现导致细胞内环磷酸腺苷(cAMP)持续(大于或等于8小时)升高的各种刺激会引起细胞膜中CFTR表达的显著且特异性增加,并伴随Cl-分泌的激活。通过环磷酸腺苷类似物或环磷酸腺苷诱导剂进行额外的短期激活可进一步激活Cl-分泌。转录或翻译的阻滞剂在很大程度上抑制了cAMP介导的CFTR水平诱导及其相关功能,表明诱导现象发生在转录水平。结果表明CFTR基因启动子中存在假定的环磷酸腺苷反应性(及相关)元件参与其中,并且已知这些元件可调节真核基因表达。各种刺激对这些元件的激活可能为在生化和生理水平上上调CFTR表达提供药理学工具。