听力学
听力损失
转基因小鼠
海马体
蛋白激酶B
转基因
信号转导
医学
生物
内分泌学
细胞生物学
神经科学
遗传学
基因
作者
Lina Pan,Chunrui Li,Lanxia Meng,Guoxin Zhang,Li Zou,Ye Tian,Sen Chen,Yu Sun,Dandan Su,Xingyu Zhang,Min Xiong,Tingting Xiao,Danhao Xia,Zheng‐Yuan Hong,Zhentao Zhang
出处
期刊:Nature Aging
日期:2024-03-15
卷期号:4 (4): 568-583
被引量:5
标识
DOI:10.1038/s43587-024-00592-5
摘要
Hearing loss is associated with an increased risk of Alzheimer disease (AD). However, the mechanisms of hearing loss promoting the onset of AD are poorly understood. Here we show that hearing loss aggravates cognitive impairment in both wild-type mice and mouse models of AD. Embryonic growth/differentiation factor 1 (GDF1) is downregulated in the hippocampus of deaf mice. Knockdown of GDF1 mimics the detrimental effect of hearing loss on cognition, while overexpression of GDF1 in the hippocampus attenuates the cognitive impairment induced by deafness. Strikingly, overexpression of GDF1 also attenuates cognitive impairment in APP/PS1 transgenic mice. GDF1 activates Akt, which phosphorylates asparagine endopeptidase and inhibits asparagine endopeptidase-induced synaptic degeneration and amyloid-β production. The expression of GDF1 is downregulated by the transcription factor CCAAT-enhancer binding protein-β. These findings indicate that hearing loss could promote AD pathological changes by inhibiting the GDF1 signaling pathway; thus, GDF1 may represent a therapeutic target for AD. Pan et al. demonstrate that hearing loss promotes cognitive decline in an APP/PS1 mouse model of Alzheimer disease via inhibition of the GDF1 signaling pathway, unveiling GDF1 as a therapeutic target for Alzheimer disease.
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