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血小板衍生生长因子介导的突触可塑性基因Arc/Arg3.1的诱导

Platelet-derived growth factor-mediated induction of the synaptic plasticity gene Arc/Arg3.1.

作者信息

Peng Fuwang, Yao Honghong, Bai Xuetao, Zhu Xuhui, Reiner Benjamin C, Beazely Michael, Funa Keiko, Xiong Huangui, Buch Shilpa

机构信息

Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, Nebraska 68198-5880, USA.

出版信息

J Biol Chem. 2010 Jul 9;285(28):21615-24. doi: 10.1074/jbc.M110.107003. Epub 2010 May 7.

Abstract

Platelet-derived growth factor (PDGF) is a pleiotropic protein with critical roles in both developmental as well as pathogenic processes. In the central nervous system specifically, PDGF is critical for neuronal proliferation and differentiation and has also been implicated as a neuroprotective agent. Whether PDGF also plays a role in synaptic plasticity, however, remains poorly understood. In the present study we demonstrated that in the rat hippocampal neurons PDGF regulated the expression of Arc/Arg3.1 gene that has been implicated in both synapse plasticity and long term potentiation. Relevance of these findings was further confirmed in vivo by injecting mice with intracerebral inoculations of PDGF, which resulted in a rapid induction of Arc in the hippocampus of the injected mice. PDGF induced long term potentiation in rat hippocampal slices, which was abolished by PDGF receptor-tyrosine kinase inhibitor STI-571. We also present evidence that PDGF-mediated induction of Arc/Arg3.1 involved activation of the MAPK/ERK (MEK) pathway. Additionally, induction of Arc/Arg3.1 also involved the upstream release of intracellular calcium stores, an effect that could be blocked by thapsigargin but not by EGTA. Pharmacological approach using inhibitors specific for either MAPK/ERK phosphorylation or calcium release demonstrated that the two pathways converged downstream at a common point involving activation of the immediate early gene Egr-1. Chromatin immunoprecipitation assays demonstrated the binding of Egr-1, but not Egr-3, to the Arc promoter. These findings for the first time, thus, suggest an additional role of PDGF, that of induction of Arc.

摘要

血小板衍生生长因子(PDGF)是一种多效性蛋白质,在发育过程和致病过程中都发挥着关键作用。具体而言,在中枢神经系统中,PDGF对神经元的增殖和分化至关重要,并且也被认为是一种神经保护剂。然而,PDGF是否也在突触可塑性中发挥作用,目前仍知之甚少。在本研究中,我们证明在大鼠海马神经元中,PDGF调节Arc/Arg3.1基因的表达,该基因与突触可塑性和长期增强效应均有关联。通过向小鼠脑内注射PDGF进行体内实验,进一步证实了这些发现的相关性,这导致注射小鼠海马中Arc的快速诱导。PDGF在大鼠海马切片中诱导长期增强效应,而PDGF受体酪氨酸激酶抑制剂STI-571可消除这种效应。我们还提供证据表明,PDGF介导的Arc/Arg3.1诱导涉及MAPK/ERK(MEK)途径的激活。此外,Arc/Arg3.1的诱导还涉及细胞内钙库的上游释放,这种效应可被毒胡萝卜素阻断,但不能被乙二醇双四乙酸(EGTA)阻断。使用针对MAPK/ERK磷酸化或钙释放的特异性抑制剂的药理学方法表明,这两条途径在涉及激活即早基因Egr-1的一个共同点下游汇聚。染色质免疫沉淀分析表明Egr-1而非Egr-3与Arc启动子结合。因此,这些发现首次提示了PDGF的另一个作用,即诱导Arc。

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