Ito E, Sonnenberg J L, Narayanan R
Department of Molecular Genetics, Roche Research Center, Nutley, New Jersey 07110.
Oncogene. 1989 Oct;4(10):1193-9.
Rat pheochromocytoma (PC-12) cells respond to nerve growth factor (NGF) by cessation of cell division and by expression of several properties resembling those of differentiated sympathetic neurons. Within minutes after addition, NGF rapidly stimulates transient expression of c-fos. To investigate the possible role of c-fos in NGF-induced differentiation, activated mouse c-fos genes were introduced into PC-12 cells by electroporation. Constitutive expression of fos inhibited NGF-induced differentiation although transfected cells harbored intact NGF receptors. Dibutyryl cyclic AMP (db cAMP) and basic fibroblast growth factor (b-FGF)-induced differentiation were also inhibited. Transcriptional activation of c-fos, c-jun, and ornithine decarboxylase (ODC) by NGF was down-regulated, whereas expression of egr-1 was unaffected in PC-12 fos clones. These results suggest that deregulated expression of fos can interfere with the normal role of NGF in neuronal differentiation.
大鼠嗜铬细胞瘤(PC - 12)细胞通过停止细胞分裂以及表达一些类似于分化交感神经元的特性来对神经生长因子(NGF)作出反应。添加NGF后几分钟内,它会迅速刺激c - fos的瞬时表达。为了研究c - fos在NGF诱导分化中的可能作用,通过电穿孔将活化的小鼠c - fos基因导入PC - 12细胞。尽管转染细胞具有完整的NGF受体,但fos的组成型表达抑制了NGF诱导的分化。二丁酰环磷腺苷(db cAMP)和碱性成纤维细胞生长因子(b - FGF)诱导的分化也受到抑制。在PC - 12 fos克隆中,NGF对c - fos、c - jun和鸟氨酸脱羧酶(ODC)的转录激活被下调,而egr - 1的表达未受影响。这些结果表明,fos的失控表达会干扰NGF在神经元分化中的正常作用。