Billestrup N, Mitchell R L, Vale W, Verma I M
Clayton Foundation Laboratories for Peptide Biology, Salk Institute, La Jolla, California 92037.
Mol Endocrinol. 1987 Apr;1(4):300-5. doi: 10.1210/mend-1-4-300.
GH-releasing factor (GRF) and somatostatin regulates the secretion and biosynthesis of GH as well as the proliferation of GH-producing cells. In order to further characterize the mitogenic effect of GRF, we studied the expression of the proto-oncogene c-fos in primary pituitary cells. Maximal induction of c-fos mRNA was observed 20-60 min after stimulation with 5 nM GRF, returning to basal levels after 2 h. Somatostatin-14 (5 nM) partially inhibited the GRF induced c-fos expression. Forskolin and phorbol 12, 13 dibutyrate induced c-fos gene in cultured primary pituitary cells with similar kinetics. Transcription of the fos gene was accompanied by biosynthesis of the fos protein. Indirect immunofluorescence using a fos specific antibody, showed exclusive nuclear localization of the fos protein. These data demonstrate that GRF and somatostatin, in addition to regulating GH secretion and somatotroph proliferation, can also regulate the expression of c-fos proto-oncogene in primary somatotrophs.
生长激素释放因子(GRF)和生长抑素调节生长激素的分泌和生物合成以及生长激素分泌细胞的增殖。为了进一步明确GRF的促有丝分裂作用,我们研究了原癌基因c-fos在原代垂体细胞中的表达。在用5 nM GRF刺激后20 - 60分钟观察到c-fos mRNA的最大诱导,2小时后恢复到基础水平。生长抑素-14(5 nM)部分抑制GRF诱导的c-fos表达。福斯高林和佛波酯12,13 - 二丁酸酯以相似的动力学在培养的原代垂体细胞中诱导c-fos基因。fos基因的转录伴随着fos蛋白的生物合成。使用fos特异性抗体的间接免疫荧光显示fos蛋白仅定位于细胞核。这些数据表明,GRF和生长抑素除了调节生长激素分泌和生长激素分泌细胞增殖外,还可调节原代生长激素分泌细胞中原癌基因c-fos的表达。