Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA; Harvard Stem Cell Institute, Harvard University, Cambridge, MA 02138, USA.
Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA; Harvard Stem Cell Institute, Harvard University, Cambridge, MA 02138, USA.
Cell Rep. 2019 Jan 29;26(5):1143-1156.e5. doi: 10.1016/j.celrep.2019.01.019.
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease affecting both upper and lower motor neurons (MNs). To date, its underlying mechanisms have yet to be clarified completely, and there are no truly effective treatments. Here, we show that MAP4K4, a MAP kinase family member, regulates MN death, with its suppression not only promoting survival but preventing neurite degeneration and decreasing mutant SOD1 levels through autophagy activation. Moreover, we report that MAP4K4 signaling specifically modulates MN viability via phosphorylated JNK3 and activation of the canonical c-Jun apoptotic pathway. Finally, we show the feasibility of MAP4K4 as a drug target by using an available MAP4K4-specific inhibitor, which improves survival of ESC and/or iPSC-derived MNs and MNs cultured from mouse spinal cords. In summary, our studies highlight a MAP4K4-initiated signaling cascade that induces MN degeneration, shedding light on the mechanism underlying MN degeneration and providing a druggable target for ALS therapeutics.
肌萎缩侧索硬化症(ALS)是一种致命的神经退行性疾病,影响上下运动神经元(MNs)。迄今为止,其潜在机制尚未完全阐明,也没有真正有效的治疗方法。在这里,我们表明 MAP4K4,一种 MAP 激酶家族成员,调节 MN 死亡,其抑制不仅促进存活,而且通过自噬激活防止神经突退化和降低突变 SOD1 水平。此外,我们报告 MAP4K4 信号通过磷酸化 JNK3 和激活经典的 c-Jun 凋亡途径特异性调节 MN 的存活。最后,我们通过使用一种可用的 MAP4K4 特异性抑制剂证明了 MAP4K4 作为药物靶点的可行性,该抑制剂可提高 ESC 和/或 iPSC 衍生的 MNs 和从小鼠脊髓培养的 MNs 的存活率。总之,我们的研究强调了 MAP4K4 引发的信号级联反应,该反应导致 MN 退化,为 MN 退化的机制提供了启示,并为 ALS 治疗提供了一个可药物治疗的靶点。