Eukaryotic Gene Expression Laboratory, National Institute of Immunology, New Delhi, India.
Eukaryotic Gene Expression Laboratory, National Institute of Immunology, New Delhi, India.
J Biol Chem. 2024 Sep;300(9):107698. doi: 10.1016/j.jbc.2024.107698. Epub 2024 Aug 22.
Aberrant activation of the cell cycle of terminally differentiated neurons results in their apoptosis and is known to contribute to neuronal loss in various neurodegenerative disorders like Alzheimer's Disease. However, the mechanisms that regulate cell cycle-related neuronal apoptosis are poorly understood. We identified several miRNA that are dysregulated in neurons from a transgenic APP/PS1 mouse model for AD (TgAD). Several of these miRNA are known to and/or are predicted to target cell cycle-related genes. Detailed investigation on miR-449a revealed the following: a, it promotes neuronal differentiation by suppressing the neuronal cell cycle; b, its expression in cortical neurons was impaired in response to amyloid peptide Aβ; c, loss of its expression resulted in aberrant activation of the cell cycle leading to apoptosis. miR-449a may prevent cell cycle-related neuronal apoptosis by targeting cyclin D1 and protein phosphatase CDC25A, which are important for G1-S transition. Importantly, the lentiviral-mediated delivery of miR-449a in TgAD mouse brain significantly reverted the defects in learning and memory, which are associated with AD.
细胞周期的异常激活会导致终末分化神经元的凋亡,这已被证实是多种神经退行性疾病(如阿尔茨海默病)中神经元丢失的原因。然而,调节与细胞周期相关的神经元凋亡的机制还知之甚少。我们在 AD 的转基因 APP/PS1 小鼠模型(TgAD)的神经元中鉴定出了几种失调的 miRNA。其中一些 miRNA 已知和/或预测靶向与细胞周期相关的基因。对 miR-449a 的详细研究揭示了以下几点:a,它通过抑制神经元细胞周期来促进神经元分化;b,其在皮质神经元中的表达对淀粉样肽 Aβ 有反应而受损;c,其表达的缺失导致细胞周期的异常激活,进而导致凋亡。miR-449a 可能通过靶向细胞周期 G1-S 转换的重要蛋白 cyclin D1 和蛋白磷酸酶 CDC25A 来预防与细胞周期相关的神经元凋亡。重要的是,miR-449a 在 TgAD 小鼠大脑中的慢病毒介导传递显著逆转了与 AD 相关的学习和记忆缺陷。