Wood K W, Qi H, D'Arcangelo G, Armstrong R C, Roberts T M, Halegoua S
Department of Cellular and Molecular Biology, Dana-Farber Cancer Institute, Boston, MA 02115.
Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5016-20. doi: 10.1073/pnas.90.11.5016.
The neuron-like differentiation of PC12 cells is induced by nerve growth factor (NGF) through stimulation of a membrane-bound protooncoprotein signaling pathway containing the NGF receptor Trk, the tyrosine kinase Src, and the GTP-binding protein Ras. The Raf-1 and B-raf protooncogenes encode cytoplasmic serine/threonine kinases that are stimulated by NGF in a Ras-dependent manner. To investigate the possible roles of cytoplasmic Raf kinases in eliciting neuronal differentiation, we have expressed the activated Raf-1 oncogene in PC12 cells. Expression of the raf oncogene results in the elaboration of a neuron-like phenotype, including neurite growth and the induction of the NGF-responsive genes NGFI-A and transin. The actions of activated Raf-1 and NGF are not additive. Furthermore, activated Raf-1 oncoprotein can prime cells for transcription-independent neurite growth by NGF and can elicit rapid neurite growth from NGF-primed cells. Our data indicate that the pathways utilized by NGF and activated raf to effect PC12 differentiation overlap and lead to the suggestion that cellular raf kinase activities play significant roles in transducing the differentiating signals of neuronal growth factors.
神经生长因子(NGF)通过刺激包含NGF受体Trk、酪氨酸激酶Src和GTP结合蛋白Ras的膜结合原癌蛋白信号通路,诱导PC12细胞向神经元样分化。Raf-1和B-raf原癌基因编码细胞质丝氨酸/苏氨酸激酶,它们以Ras依赖的方式被NGF激活。为了研究细胞质Raf激酶在引发神经元分化中的可能作用,我们在PC12细胞中表达了活化的Raf-1癌基因。raf癌基因的表达导致形成神经元样表型,包括神经突生长以及诱导NGF反应性基因NGFI-A和反式激活蛋白。活化的Raf-1和NGF的作用并非相加性的。此外,活化的Raf-1癌蛋白可使细胞对NGF诱导的非转录依赖性神经突生长产生反应,并能从经NGF预处理的细胞中引发快速的神经突生长。我们的数据表明,NGF和活化的raf用于影响PC12分化的信号通路重叠,这表明细胞raf激酶活性在转导神经元生长因子的分化信号中起重要作用。