粒体自噬
调节器
品脱1
神经科学
神经保护
线粒体
脱甲基酶
帕金森病
生物
神经退行性变
疾病
功能(生物学)
细胞生物学
失调家庭
磷脂病
负调节器
氧化应激
表型
人类疾病
核糖核酸
损失函数
医学
神经病理学
化学
氧化磷酸化
平衡
机制(生物学)
作者
Y Li,S. M. Yu,Ke Lü,Yujie Zhang,Mingjie Dong,You Peng,Liang Xue,Waleed Alam,Yuxuan Shui,Yi Zhou,Wuyunhan Ma,Meng Bao,Peiming Li,Peiyi Luo,Tiezhan Lu,Jiajia Li,Kang Zhang,Yuying Wang,Shuchen Yang,Na Yin
标识
DOI:10.1002/advs.202522572
摘要
Amyloid-beta (Aβ) aggregation, mitochondrial dysfunction, and cognitive decline are hallmarks of Alzheimer's disease (AD), but its initiating molecular events remain unknown. Given that RNA modifications regulate neurodevelopment and neurodegeneration, we explore their functional role in 5xFAD mice, an Aβ AD model. We discover that N1-methyladenosine (m1A) is the most altered RNA modification, and that its regulator demethylase, ALKBH3 is upregulated. Strikingly, Alkbh3 reduction decreases Aβ plaques and restores cognition. Conversely, elevated ALKBH3 levels, observed in AD patients, compromise neuronal morphology and mitochondrial function by impairing mitophagy (degradation of dysfunctional mitochondria), a known driver of neuronal dysfunction. Mechanistically, we reveal that ALKBH3 removes m1A from PINK1 mRNA, the mitophagy master regulator. Given that ALKBH3 is elevated in human AD, causally linked to mitophagy impairment, and confers neuroprotection when depleted, we present ALKBH3 as a mechanistically validated therapeutic target in AD.
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