Zhang Yuan, Lv Xuan, Bai Ying, Zhu Xinjian, Wu Xiaodong, Chao Jie, Duan Ming, Buch Shilpa, Chen Ling, Yao Honghong
Department of Pharmacology, Medical School of Southeast University, 87 Dingjiaqiao, Nanjing, Jiangsu, 210009, China.
Department of Physiology, Medical School of Southeast University, 87 Dingjiaqiao, Nanjing, 210009, China.
J Neuroinflammation. 2015 Feb 17;12:29. doi: 10.1186/s12974-015-0250-7.
Although it has been documented that methamphetamine induces astrocyte activation, the mechanism(s) underlying this effect remain poorly understood. We thus sought to examine the molecular mechanisms involved in methamphetamine-mediated activation of astrocytes with a focus on the role of sigma-1 receptor (σ-1R) in this process.
The expression of σ-1R and glial fibrillary acidic protein (GFAP) was examined by reverse transcription PCR (RT-PCR), real-time PCR, Western blot, and immunofluorescent staining; phosphorylation of cell signaling pathways was detected by Western blot analysis. Immunoprecipitation was used to determine the interaction between σ-1R and p-Src. Chromatin immunoprecipitation (ChIP) assay was employed to discern the binding of cAMP-response element-binding protein (CREB) with the promoter of σ-1R. The role of σ-1R in astrocyte activation was further validated in σ-1R knockout (KO) mice by Western blot combined with immunofluorescent staining.
Exposure of primary rat astrocytes to methamphetamine increased the expression of σ-1R via the activation of Src, ERK mitogen-activated protein kinase, and downstream CREB pathways. Subsequently, CREB translocated into nucleus and interacted with the promoter of σ-1R resulting in increased expression of σ-1R with a concomitant increase in expression of GFAP. This effect was inhibited in cells treated with the σ-1R antagonist-BD1047, thereby implicating the role of σ-1R in the activation of astrocytes. In vivo relevance of these findings was further corroborated in σ-1R KO mice that were administered methamphetamine. In the methamphetamine administered mice, there was a failure of the drug to induce activation of astrocytes, an effect that was evident in wild-type (WT) mice exposed to methamphetamine.
The study presented herein demonstrates that methamphetamine-mediated activation of astrocytes involved up-regulation of σ-1R through a positive-feedback mechanism. Understanding the regulation of σ-1R expression could provide insights into the development of potential therapeutic strategies for astrocyte activation induced by methamphetamine.
尽管已有文献记载甲基苯丙胺可诱导星形胶质细胞活化,但其潜在机制仍知之甚少。因此,我们试图研究甲基苯丙胺介导的星形胶质细胞活化所涉及的分子机制,重点关注σ-1受体(σ-1R)在此过程中的作用。
通过逆转录聚合酶链反应(RT-PCR)、实时PCR、蛋白质印迹法和免疫荧光染色检测σ-1R和胶质纤维酸性蛋白(GFAP)的表达;通过蛋白质印迹分析检测细胞信号通路的磷酸化。免疫沉淀法用于确定σ-1R与磷酸化Src(p-Src)之间的相互作用。采用染色质免疫沉淀(ChIP)分析来识别环磷酸腺苷反应元件结合蛋白(CREB)与σ-1R启动子的结合。通过蛋白质印迹结合免疫荧光染色在σ-1R基因敲除(KO)小鼠中进一步验证σ-1R在星形胶质细胞活化中的作用。
原代大鼠星形胶质细胞暴露于甲基苯丙胺后,通过Src、细胞外信号调节激酶(ERK)丝裂原活化蛋白激酶和下游CREB通路的激活增加了σ-1R的表达。随后,CREB易位至细胞核并与σ-1R的启动子相互作用,导致σ-1R表达增加,同时GFAP表达也随之增加。在用σ-1R拮抗剂BD1047处理的细胞中,这种效应受到抑制,从而表明σ-1R在星形胶质细胞活化中的作用。这些发现的体内相关性在给予甲基苯丙胺的σ-1R KO小鼠中得到进一步证实。在给予甲基苯丙胺 的小鼠中,该药物未能诱导星形胶质细胞活化,而在暴露于甲基苯丙胺的野生型(WT)小鼠中这种效应很明显。
本文提出的研究表明,甲基苯丙胺介导的星形胶质细胞活化通过正反馈机制涉及σ-1R的上调。了解σ-1R表达的调节可能为开发针对甲基苯丙胺诱导的星形胶质细胞活化的潜在治疗策略提供见解。