Cappelletti Graziella, Galbiati Mariarita, Ronchi Cristina, Maggioni Maria Grazia, Onesto Elisa, Poletti Angelo
Department of Biology, University of Milan, Milan, Italy.
J Neurosci Res. 2007 Sep;85(12):2702-13. doi: 10.1002/jnr.21235.
Neuritin is a small, highly conserved GPI-anchored protein involved in neurite outgrowth. We have analyzed the involvement of neuritin in NGF-induced differentiation of PC12 cells by investigating the time-course of neuritin expression, the effects of its overexpression or silencing, and the possible mechanisms of its regulation and action. Real-time PCR analysis has shown that neuritin gene is upregulated by NGF in PC12 cells hours before neurite outgrowth becomes appreciable. PC12 cells transfected with a plasmid expressing neuritin display a significant increase in the response to NGF: 1) in the levels of SMI312 positive phosphorylated neurofilament proteins (markers for axonal processes) and tyrosine hydroxylase; 2) in the percentage of cells bearing neurites; as well as 3) in the average length of neurites when compared to control cells. On the contrary, neuritin silencing significantly reduces neurite outgrowth. These data suggest that neuritin is a modulator of NGF-induced neurite extension in PC12 cells. We also showed that neuritin potentiated the NGF-induced differentiation of PC12 cells without affecting TrkA or EGF receptor mRNAs expression. Moreover, the S-methylisothiourea (MIU), a potent inhibitor of inducible nitric oxide synthases, partially counteracts the NGF-mediated neuritin induction. These data suggest that NGF regulates neuritin expression in PC12 cells via the signaling pathway triggered by NO. This study reports the first evidence that neuritin plays a role in modulating neurite outgrowth during the progression of NGF-induced differentiation of PC12 cells. PC12 cells could be considered a valuable model to unravel the mechanism of action of neuritin on neurite outgrowth. (c) 2007 Wiley-Liss, Inc.
神经突素是一种参与神经突生长的小型、高度保守的糖基磷脂酰肌醇锚定蛋白。我们通过研究神经突素表达的时间进程、其过表达或沉默的影响以及其调节和作用的可能机制,分析了神经突素在神经生长因子(NGF)诱导的PC12细胞分化中的作用。实时PCR分析表明,在神经突生长明显出现之前数小时,NGF可使PC12细胞中的神经突素基因上调。用表达神经突素的质粒转染的PC12细胞对NGF的反应显著增加:1)SMI312阳性磷酸化神经丝蛋白(轴突过程的标志物)和酪氨酸羟化酶水平;2)有神经突的细胞百分比;3)与对照细胞相比,神经突的平均长度。相反,神经突素沉默显著减少神经突生长。这些数据表明神经突素是PC12细胞中NGF诱导的神经突延伸的调节剂。我们还表明,神经突素增强了NGF诱导的PC12细胞分化,而不影响TrkA或表皮生长因子受体mRNA的表达。此外,诱导型一氧化氮合酶的强效抑制剂S-甲基异硫脲(MIU)部分抵消了NGF介导的神经突素诱导。这些数据表明,NGF通过一氧化氮触发的信号通路调节PC12细胞中神经突素的表达。本研究首次报道了神经突素在NGF诱导的PC12细胞分化过程中调节神经突生长中发挥作用的证据。PC12细胞可被视为揭示神经突素对神经突生长作用机制的有价值模型。(c)2007威利-利斯公司。