Department of Anatomy, Korea University College of Medicine, Seoul, Republic of Korea.
Department of Physiology, Korea University College of Medicine, Seoul, Republic of Korea.
Int J Neuropsychopharmacol. 2019 Jun 3;22(6):402-414. doi: 10.1093/ijnp/pyz016.
Leukemia inhibitory factor, a novel myokine, is known to be associated with neural function, but the underlying molecular mechanism remains unclear.
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.
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.
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.
白血病抑制因子是一种新型的肌肉因子,已知与神经功能有关,但潜在的分子机制尚不清楚。
使用 HT-22 小鼠海马细胞、原代海马细胞和阿尔茨海默病果蝇模型来确定白血病抑制因子对神经元的影响。采用免疫印迹分析和免疫荧光法分析其生物学机制。
白血病抑制因子在海马细胞中以磷脂酰肌醇 3-激酶依赖的方式增加 Akt 磷酸化。白血病抑制因子还增加了雷帕霉素的哺乳动物靶蛋白和下游 S6K 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和转录激活物的磷酸化。白血病抑制因子通过 Akt 和细胞外信号调节激酶增加 c-fos 的表达。白血病抑制因子通过阻断淀粉样β介导的胰岛素受体下调,阻止淀粉样β诱导的神经活力抑制和葡萄糖摄取损伤。白血病抑制因子阻断了淀粉样β诱导的自噬标记物微管相关蛋白 1A/1B-轻链 3 的诱导。此外,在原代制备的海马细胞中,白血病抑制因子刺激 Akt 和细胞外信号调节激酶,表明白血病抑制因子在体内具有生理相关性。在阿尔茨海默病的果蝇模型中观察到白血病抑制因子抑制自噬标记物轻链 3II。
这些结果表明,白血病抑制因子通过 Akt/细胞外信号调节激酶介导的 c-fos 诱导来保护免受淀粉样β诱导的神经毒性,因此表明白血病抑制因子是阿尔茨海默病的一种潜在药物。