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神经生长因子对PC12细胞神经突生长的自分泌调节

Autocrine regulation of neurite outgrowth from PC12 cells by nerve growth factor.

作者信息

Gill J S, Schenone A E, Podratz J L, Windebank A J

机构信息

Molecular Neuroscience Program, Mayo Clinic and Mayo Foundation, 1501 Guggenheim Building, 200 First Street SW, Rochester, MN 55905, USA.

出版信息

Brain Res Mol Brain Res. 1998 Jun 1;57(1):123-31. doi: 10.1016/s0169-328x(98)00080-1.

Abstract

The PC12 cell line may be used as a model of NGF-induced neuronal differentiation. Exposure to NGF is accompanied by extension of neurites, cessation of growth and differentiation into cells resembling sympathetic neurons. In this study neurite outgrowth from PC12 cells was induced in serum-free, NGF-free medium conditions. Neurite outgrowth in serum-free conditions was abolished by exposure to anti-NGF antisera. Reverse transcription combined with polymerase chain reaction (RT-PCR) and in situ hybridization of PC12 cells in serum-free medium conditions revealed NGF transcripts. Western blot analysis of these cells revealed tyrosine phosphorylation of the high affinity NGF receptor (TrkA/gp140) and activation of a downstream signal cascade element, ERK-1/MAP kinase. NGF was also detected by a specific enzyme-linked immunoabsorbant assay (ELISA) revealing picogram levels of protein in conditioned medium and cell lysates. Survival of embryonic rat dorsal root ganglion neurons was maintained in cultures grown in this serum-free conditioned medium. This demonstrated that NGF may act as an autocrine or paracrine growth factor for PC12 cell differentiation.

摘要

PC12细胞系可作为神经生长因子(NGF)诱导神经元分化的模型。暴露于NGF会伴随着神经突的延伸、生长停止以及分化为类似交感神经元的细胞。在本研究中,在无血清、无NGF的培养基条件下诱导PC12细胞长出神经突。在无血清条件下,暴露于抗NGF抗血清会消除神经突的生长。在无血清培养基条件下,对PC12细胞进行逆转录聚合酶链反应(RT-PCR)和原位杂交,结果显示有NGF转录本。对这些细胞进行蛋白质免疫印迹分析,结果显示高亲和力NGF受体(TrkA/gp140)发生酪氨酸磷酸化,并且下游信号级联元件ERK-1/丝裂原活化蛋白激酶被激活。通过特异性酶联免疫吸附测定(ELISA)也检测到了NGF,结果显示在条件培养基和细胞裂解物中有皮克水平的蛋白质。在这种无血清条件培养基中培养的胚胎大鼠背根神经节神经元得以存活。这表明NGF可能作为一种自分泌或旁分泌生长因子促进PC12细胞分化。

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