Xiao Jingnan, Zhou Qiong, Liu Yuechueng
Department of Pathology, University of Oklahoma School of Medicine, Oklahoma City, Oklahoma, USA.
J Neurosci Res. 2002 Jul 1;69(1):104-9. doi: 10.1002/jnr.10260.
The rat pheochromocytoma PC12 cells differentiate into neuronal-like cells in response to treatment with neurotrophins. The cells have been extensively used for investigating neuronal differentiation and axonal growth. Here we report the isolation of a variant PC12 cell line, named PC12-N1, which spontaneously differentiates and extends neuritic processes. The PC12-N1 cells expressed many neuronal specific proteins, including the synaptosomal associated protein of 25 kDa (SNAP-25), synaptotagmin, and synaptobrevin (also known as VAMP). The cells also expressed neurofilament protein of 68 kDa, a marker for differentiated neurons. In addition to the spontaneous neurite outgrowth, the PC12-N1 cells showed a marked increase in neurite outgrowth upon treatment with nerve growth factor (NGF), basic fibroblast growth factor (bFGF), and cyclic AMP (cAMP). The activation of mitogen-activated protein (MAP) kinases was examined by immunoblot analysis using phospho-specific antibodies. No overactivation was observed with ERK1/2 or p38. However, the c-Jun N-terminal kinase JNK/SAPK was activated approximately 10-fold over the parental PC12 cells. These results suggest that activation of JNK/SAPK may be involved in the spontaneous neurite extension in the PC12-N1 cells. Moreover, the PC12-N1 cells may be used as a model for investigating molecular signaling mechanisms underlying neuronal differentiation and axonal outgrowth.
大鼠嗜铬细胞瘤PC12细胞在神经营养因子的作用下可分化为神经元样细胞。这些细胞已被广泛用于研究神经元分化和轴突生长。在此,我们报告了一种变异的PC12细胞系的分离,命名为PC12-N1,它能自发分化并延伸神经突。PC12-N1细胞表达了许多神经元特异性蛋白,包括25 kDa的突触体相关蛋白(SNAP-25)、突触结合蛋白和突触小泡蛋白(也称为VAMP)。这些细胞还表达了68 kDa的神经丝蛋白,这是分化神经元的一个标志物。除了自发的神经突生长外,PC12-N1细胞在接受神经生长因子(NGF)、碱性成纤维细胞生长因子(bFGF)和环磷酸腺苷(cAMP)处理后,神经突生长显著增加。使用磷酸化特异性抗体通过免疫印迹分析检测丝裂原活化蛋白(MAP)激酶的激活情况。未观察到ERK1/2或p38的过度激活。然而,c-Jun N端激酶JNK/SAPK的激活程度比亲代PC12细胞高出约10倍。这些结果表明,JNK/SAPK的激活可能参与了PC12-N1细胞中自发的神经突延伸。此外,PC12-N1细胞可作为研究神经元分化和轴突生长潜在分子信号机制的模型。