Burstein D E, Seeley P J, Greene L A
J Cell Biol. 1985 Sep;101(3):862-70. doi: 10.1083/jcb.101.3.862.
LiCl (2.5-20 mM) reversibly suppressed nerve growth factor (NGF)-induced neurite outgrowth by cultured rat PC 12 pheochromocytoma cells. Similar concentrations of LiCl also reversibly blocked NGF-dependent regeneration of neurites by PC12 cells that had been primed by long-term pre-exposure to NGF and by cultured newborn mouse sympathetic neurons. In contrast, transcription-dependent responses of PC12 cells to NGF such as priming and induction of the NGF-inducible large external glycoprotein, occurred despite the presence of Li+. SDS PAGE analysis of total cellular phosphoproteins (labeled by 2-h exposure to 32P-orthophosphate) from neurite-bearing primed PC12 cells revealed that Li+ reversibly inhibited the phosphorylation of a band of Mr 64,000 that was barely detectable in NGF-untreated PC12 cells. However, Li+ did not appear to affect the labeling of other phosphoproteins in either NGF-primed or untreated PC12 cultures, nor did it affect the rapid increase in phosphorylation of several proteins that occurs when NGF is first added to unprimed cultures. Several criteria indicated that the NGF-inducible phosphoprotein of Mr 64,000 is a microtubule-associated protein (MAP). Of the NGF-inducible phosphorylated MAPs that have been detected in PC12 cells (Mr 64,000, 72,000, 80,000, and 320,000), several (Mr 64,000, 72,000, and 80,000) were found to be substantially less phosphorylated in the presence of Li+. Neither a phorbol ester tumor promotor nor permeant cAMP analogs reversed the inhibitory effects of Li+ on neurite outgrowth or on phosphorylation of the component of Mr 64,000. Microtubules are a major and required constituent of neurites, and MAPs may regulate the assembly and stability of neuritic microtubules. The observation that Li+ selectively inhibits NGF-induced neurite outgrowth and MAP phosphorylation suggests a possible causal relationship between these two events.
氯化锂(2.5 - 20 mM)可逆转地抑制培养的大鼠嗜铬细胞瘤PC12细胞的神经生长因子(NGF)诱导的神经突生长。相似浓度的氯化锂也可逆转地阻断由长期预先暴露于NGF而致敏的PC12细胞以及培养的新生小鼠交感神经元的NGF依赖性神经突再生。相比之下,尽管存在锂离子,PC12细胞对NGF的转录依赖性反应,如致敏和诱导NGF诱导的大细胞外糖蛋白,仍会发生。对来自带有神经突的致敏PC12细胞的总细胞磷蛋白(通过暴露于32P - 正磷酸盐2小时进行标记)进行SDS - PAGE分析显示,锂离子可逆转地抑制一条分子量为64,000的条带的磷酸化,该条带在未用NGF处理的PC12细胞中几乎检测不到。然而,锂离子似乎既不影响在NGF致敏或未处理的PC12培养物中其他磷蛋白的标记,也不影响首次将NGF添加到未致敏培养物时几种蛋白质磷酸化的快速增加。多项标准表明,分子量为64,000的NGF诱导的磷蛋白是一种微管相关蛋白(MAP)。在PC12细胞中检测到的NGF诱导的磷酸化MAPs(分子量为64,000、72,000、80,000和320,000)中,有几种(分子量为64,000、72,000和80,000)在有锂离子存在时磷酸化程度明显降低。佛波酯肿瘤促进剂或渗透性cAMP类似物均不能逆转锂离子对神经突生长或对分子量为64,000的成分磷酸化的抑制作用。微管是神经突的主要且必需的组成部分,而MAPs可能调节神经突微管的组装和稳定性。锂离子选择性抑制NGF诱导的神经突生长和MAP磷酸化这一观察结果表明这两个事件之间可能存在因果关系。