...
首页> 外文期刊>The international journal of neuropsychopharmacology >LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells
【24h】

LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells

机译:LIF,一种新型的肌动蛋白,通过Akt介导的自噬信号在海马细胞中防御淀粉样β诱导的神经毒性。

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Background Leukemia inhibitory factor, a novel myokine, is known to be associated with neural function, but the underlying molecular mechanism remains unclear. Methods HT-22 mouse hippocampal cells, primary hippocampal cells, and Drosophila Alzheimer’s disease model were used to determine the effect of leukemia inhibitory factor on neurons. Immunoblot analysis and immunofluorescence method were used to analyze biological mechanism. Results Leukemia inhibitory factor increased Akt phosphorylation in a phosphoinositide-3-kinase-dependent manner in hippocampal cells. Leukemia inhibitory factor also increased the phosphorylation of the mammalian target of rapamycin and the downstream S6K. Leukemia inhibitory factor stimulated the phosphorylation of signal transducer and activator of transcription via extracellular signal-regulated kinases. Leukemia inhibitory factor increased c-fos expression through both Akt and extracellular signal-regulated kinases. Leukemia inhibitory factor blocked amyloid β-induced neural viability suppression and inhibited amyloid β-induced glucose uptake impairment through the block of amyloid β-mediated insulin receptor downregulation. Leukemia inhibitory factor blocked amyloid β-mediated induction of the autophagy marker, microtubule-associated protein 1A/1B-light chain 3. Additionally, in primary prepared hippocampal cells, leukemia inhibitory factor stimulated Akt and extracellular signal-regulated kinase, demonstrating that leukemia inhibitory factor has physiological relevance in vivo. Suppression of the autophagy marker, light chain 3II, by leukemia inhibitory factor was observed in a Drosophila model of Alzheimer’s disease. Conclusions These results demonstrate that leukemia inhibitory factor protects against amyloid β-induced neurotoxicity via Akt/extracellular signal-regulated kinase-mediated c-fos induction, and thus suggest that leukemia inhibitory factor is a potential drug for Alzheimer’s disease.
机译:背景白血病抑制因子,一种新型的肌动蛋白,已知与神经功能有关,但其潜在的分子机制仍不清楚。方法采用HT-22小鼠海马细胞,原代海马细胞和果蝇阿尔茨海默氏病模型确定白血病抑制因子对神经元的影响。免疫印迹分析和免疫荧光法分析其生物学机制。结果白血病抑制因子以磷酸肌醇3激酶依赖性方式增加海马细胞中Akt的磷酸化。白血病抑制因子还增加了雷帕霉素和下游S6K哺乳动物靶标的磷酸化。白血病抑制因子通过细胞外信号调节激酶刺激信号转导子和转录激活子的磷酸化。白血病抑制因子通过Akt和细胞外信号调节激酶增加c-fos表达。白血病抑制因子通过阻止β淀粉样蛋白介导的胰岛素受体下调,阻断了β淀粉样蛋白引起的神经活力抑制,并抑制β淀粉样蛋白引起的葡萄糖摄取障碍。白血病抑制因子阻断了淀粉样蛋白β介导的自噬标记物微管相关蛋白1A / 1B-轻链3的诱导。此外,在原代准备的海马细胞中,白血病抑制因子刺激了Akt和细胞外信号调节激酶,证明了白血病抑制作用因子在体内具有生理相关性。在阿尔茨海默氏病的果蝇模型中观察到白血病抑制因子抑制了自噬标记轻链3II。结论这些结果表明,白血病抑制因子可通过Akt /细胞外信号调节激酶介导的c-fos诱导来防止淀粉样β诱导的神经毒性,因此表明白血病抑制因子是治疗阿尔茨海默氏病的潜在药物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号