Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, Ohio, USA.
Department of Neurology and.
J Clin Invest. 2020 Jul 1;130(7):3403-3405. doi: 10.1172/JCI137908.
AMPK is a heterotrimeric complex that serves as a major sensor of energy status in eukaryotic cells. Accumulating evidence depicts a complex role of dysregulated AMPK signaling in Alzheimer's disease (AD). In this issue of the JCI, Zimmermann et al. report on their investigation of AD-specific differential expression of AMPKα1 and AMPKα2 isoforms of the catalytic subunit and demonstrate that genetic reduction of AMPKα1, but not AMPKα2, rescued cognitive decline in AD mouse models. These findings reveal an isoform-specific role of AMPKα in the pathogenesis of AD, which likely provides a more precise target for future therapeutic development.
AMPK 是一种异三聚体复合物,作为真核细胞能量状态的主要传感器。越来越多的证据表明,失调的 AMPK 信号在阿尔茨海默病 (AD) 中发挥着复杂的作用。在本期 JCI 中,Zimmermann 等人报告了他们对 AD 中催化亚基 AMPKα1 和 AMPKα2 同工型的特异性差异表达的研究,并证明 AMPKα1 的遗传减少,而不是 AMPKα2,可挽救 AD 小鼠模型的认知衰退。这些发现揭示了 AMPKα 在 AD 发病机制中的同工型特异性作用,这可能为未来的治疗开发提供更精确的靶点。