Monstein H J, Pedersen K, Haahr P M
Department of Clinical Biochemistry (KK 3013), State University Hospital (Rigshospitalet), Copenhagen, Denmark.
Neuropeptides. 1992 Oct;23(2):107-13. doi: 10.1016/0143-4179(92)90087-d.
The effect of fetal-calf serum (FCS) and Forskolin (FKN) on cholecystokinin (CCK) and proto-oncogene c-fos mRNA expression in the human neuroblastoma cell line SK-N-MC, cultured in serum free medium was studied by Northern blot analysis and nuclear run-off transcription analysis. Addition of FCS or FKN gradually increased the basal CCK mRNA level approximately four to six-fold after 2-4 h. In contrast, a strong and transient increase of the c-fos mRNA-level was observed, approximately forty to fifty-fold after 50-60 min over unstimulated cells. Nuclear run-off transcription analysis indicates that c-fos mRNA is constitutively expressed and transcription may be further stimulated by FCS and FKN. Moreover, in SK-N-MC nuclei, transcription of the c-fos gene clearly precedes stimulated CCK-mRNA expression. This suggests that FOS, which is known to form a AP-1 heterodimer transcription complex with the proto-oncogen product, Jun, may bind to the tentative AP-1 binding site, found within the human CCK promoter and thereby modulates basal and enhanced CCK-mRNA expression in SK-N-MC cells.
采用Northern印迹分析和细胞核转录分析方法,研究了胎牛血清(FCS)和福斯高林(FKN)对在无血清培养基中培养的人神经母细胞瘤细胞系SK-N-MC中胆囊收缩素(CCK)和原癌基因c-fos mRNA表达的影响。添加FCS或FKN后,2 - 4小时内基础CCK mRNA水平逐渐增加约4至6倍。相反,观察到c-fos mRNA水平有强烈且短暂的增加,在50 - 60分钟后比未刺激的细胞增加约40至50倍。细胞核转录分析表明,c-fos mRNA组成性表达,转录可能受到FCS和FKN的进一步刺激。此外,在SK-N-MC细胞核中,c-fos基因的转录明显先于受刺激的CCK-mRNA表达。这表明,已知与原癌基因产物Jun形成AP-1异二聚体转录复合物的FOS,可能与在人CCK启动子内发现的假定AP-1结合位点结合,从而调节SK-N-MC细胞中基础和增强的CCK-mRNA表达。