Department of Biomedical Sciences, University of Guelph, Guelph, ON, Canada.
Cell Mol Neurobiol. 2013 Mar;33(2):269-82. doi: 10.1007/s10571-012-9894-3. Epub 2012 Nov 29.
The mechanisms by which nerve growth factor (NGF) increases the level of low density lipoprotein receptor-related protein (LRP1) are not known. Administration of nitric oxide synthase (NOS) inhibitors modulates several of the neurotrophic actions of NGF, including TrkA signalling pathway activation, increases in gene expression and neurite outgrowth. The present study investigated whether NGF regulates the transcription of LRP1 as well as the role of NO and the individual TrkA signalling pathways in this action of NGF. PC12 cells were transfected with luciferase reporter constructs containing various sized fragments of the LRP1 promoter and treated with NGF (50 ng/mL) to establish whether NGF altered LRP transcription. NGF significantly increased luciferase activity in all LRP1 promoter construct-transfected cells with the NGF-responsive region of the promoter identified to be present in the first 1000 bp. The non-selective NOS inhibitor N(ω)-nitro-L-arginine methylester (L-NAME; 20 mM) had no effect on the NGF-mediated increase in luciferase activity, while the inducible NOS selective inhibitor s-methylisothiourea (S-MIU; 2 mM) attenuated the NGF-induced activation of the LRP1 promoter. Pretreatment of PC12 cells with 10 μM bisindolylmaleimide 1 (BIS-1) prevented the NGF-mediated increase in LRP1 promoter activation while 50 μM U0126 partially inhibited this response. In combination with S-MIU, all of the TrkA signalling pathway inhibitors blocked the ability of NGF to increase LRP1 transcription. These data suggest the NGF-mediated increase in LRP1 levels occurs, at least in part, at the level of transcription and that NO and the TrkA signalling pathways cooperate in the modulation of LRP1 transcription.
神经生长因子(NGF)增加低密度脂蛋白受体相关蛋白(LRP1)水平的机制尚不清楚。一氧化氮合酶(NOS)抑制剂的给药调节了 NGF 的几种神经营养作用,包括 TrkA 信号通路的激活、基因表达的增加和神经突的生长。本研究探讨了 NGF 是否调节 LRP1 的转录,以及 NO 和各个 TrkA 信号通路在 NGF 这一作用中的作用。PC12 细胞用包含 LRP1 启动子各种大小片段的荧光素酶报告构建体转染,并用 NGF(50ng/ml)处理,以确定 NGF 是否改变 LRP 转录。NGF 显著增加了所有转染 LRP1 启动子构建体的细胞中的荧光素酶活性,而启动子的 NGF 反应区被鉴定为存在于前 1000bp 中。非选择性 NOS 抑制剂 N(ω)-硝基-L-精氨酸甲酯(L-NAME;20mM)对 NGF 介导的荧光素酶活性增加没有影响,而诱导型 NOS 选择性抑制剂 S-甲基异硫脲(S-MIU;2mM)减弱了 NGF 诱导的 LRP1 启动子激活。PC12 细胞用 10μM 双吲哚马来酰亚胺 1(BIS-1)预处理可阻止 NGF 介导的 LRP1 启动子激活增加,而 50μM U0126 部分抑制了这一反应。与 S-MIU 联合使用时,所有的 TrkA 信号通路抑制剂都阻断了 NGF 增加 LRP1 转录的能力。这些数据表明,NGF 介导的 LRP1 水平增加至少部分发生在转录水平,NO 和 TrkA 信号通路在 LRP1 转录的调节中合作。