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自发分化并延伸神经突的变异型PC12细胞系。

Variant PC12 cell line that spontaneously differentiates and extends neuritic processes.

作者信息

Xiao Jingnan, Zhou Qiong, Liu Yuechueng

机构信息

Department of Pathology, University of Oklahoma School of Medicine, Oklahoma City, Oklahoma, USA.

出版信息

J Neurosci Res. 2002 Jul 1;69(1):104-9. doi: 10.1002/jnr.10260.

Abstract

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.

摘要

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。

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