Klinz F J, Wolff P, Heumann R
Department of Molecular Neurobiochemistry, Ruhr-Universität Bochum, Germany.
J Neurosci Res. 1996 Dec 15;46(6):720-6. doi: 10.1002/(SICI)1097-4547(19961215)46:6<720::AID-JNR8>3.0.CO;2-H.
Nerve growth factor (NGF)-stimulated neurite outgrowth in the rat PC12 tumor cell line recently has been shown to depend on the activation of the mitogen-activated protein (MAP) kinase kinase 1 (MEK1) (Pang et al.: J Biol Chem 270:13585-13588, 1995). In this study we have analyzed whether or not function of the MAP kinase pathway is necessary for NGF-stimulated neurite outgrowth in two subtypes of primary neurons derived from the embryonic chick peripheral nervous system (PNS). Treatment of p21ras-dependent dorsal root ganglion (DRG) sensory neurons (E9) with the MEK1 inhibitor PD98059 at concentrations up to 100 microM did not prevent NGF-stimulated neurite outgrowth. At this concentration NGF-stimulated tyrosine phosphorylation of MAP kinase p42 as well as MAP kinase activity both were decreased by approximately 80%. Essentially the same results were obtained with p21ras-independent sympathetic neurons (E12). We conclude that, in contrast to the PC12 tumor cell line, NGF-stimulated MAP kinase activity is not necessary for neurite outgrowth of DRG sensory and sympathetic neurons derived from the chick PNS.
神经生长因子(NGF)刺激大鼠PC12肿瘤细胞系的神经突生长最近已被证明依赖于丝裂原活化蛋白(MAP)激酶激酶1(MEK1)的激活(庞等人:《生物化学杂志》270:13585 - 13588,1995)。在本研究中,我们分析了MAP激酶途径的功能对于源自胚胎鸡外周神经系统(PNS)的两种原代神经元亚型中NGF刺激的神经突生长是否必要。用浓度高达100微摩尔的MEK1抑制剂PD98059处理p21ras依赖性背根神经节(DRG)感觉神经元(E9),并未阻止NGF刺激的神经突生长。在此浓度下,NGF刺激的MAP激酶p42的酪氨酸磷酸化以及MAP激酶活性均降低了约80%。用p21ras非依赖性交感神经元(E12)也得到了基本相同的结果。我们得出结论,与PC12肿瘤细胞系不同,NGF刺激的MAP激酶活性对于源自鸡PNS的DRG感觉神经元和交感神经元的神经突生长不是必需的。