Autophagy is involved in oral rAAV/Aβ vaccine-induced Aβ clearance in APP/PS1 transgenic mice

被引:31
作者
Wang, He-Cheng [1 ,2 ]
Zhang, Tao [1 ,2 ]
Kuerban, Bolati [1 ,2 ]
Jin, Ying-Lan [1 ,2 ]
Le, Weidong [3 ]
Hara, Hideo [4 ]
Fan, Dong-Sheng [5 ]
Wang, Yan-Jiang [6 ]
Tabira, Takeshi [7 ]
Chui, De-Hua [1 ,2 ,5 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Neurosci Res Inst, Sch Basic Med Sci, Beijing 100191, Peoples R China
[2] Peking Univ, Hlth Sci Ctr, Dept Neurobiol, Sch Basic Med Sci, Beijing 100191, Peoples R China
[3] Dalian Med Univ, Affiliated Hosp 1, Ctr Translat Res Neurol Dis, Dalian 116011, Peoples R China
[4] Saga Univ, Fac Med, Dept Internal Med, Div Neurol, Saga 8498501, Japan
[5] Peking Univ, Hosp 3, Dept Neurol, Beijing 100191, Peoples R China
[6] Third Mil Med Univ, Daping Hosp, Dept Neurol, Chongqing 400042, Peoples R China
[7] Juntendo Univ, Grad Sch Med, Dept Neurol, Tokyo 1130033, Japan
基金
中国国家自然科学基金;
关键词
oral vaccination; autophagy; Akt/mTOR pathway; A beta clearance; Alzheimer's disease; ALZHEIMERS-DISEASE; AMYLOID-BETA; MOUSE MODEL; HYPOTHETICAL MODEL; MAMMALIAN TARGET; SENILE PLAQUES; NEURODEGENERATION; IMMUNOTHERAPY; COMPLEMENT; MEMORY;
D O I
10.1007/s12264-015-1546-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The imbalance between beta-amyloid (A beta) generation and clearance plays a fundamental role in the pathogenesis of Alzheimer's disease (AD). The sporadic form of AD is characterized by an overall impairment in A beta clearance. Immunotherapy targeting A beta clearance is believed to be a promising approach and is under active clinical investigation. Autophagy is a conserved pathway for degrading abnormal protein aggregates and is crucial for A beta clearance. We previously reported that oral vaccination with a recombinant AAV/A beta vaccine increased the clearance of A beta from the brain and improved cognitive ability in AD animal models, while the underlying mechanisms were not well understood. In this study, we first demonstrated that oral vaccination with rAAV/A beta decreased the p62 level and up-regulated the LC3BII/LC3B-I ratio in APP/PS1 mouse brain, suggesting enhanced autophagy. Further, inhibition of the Akt/mTOR pathway may account for autophagy enhancement. We also found increased anti-A beta antibodies in the sera of APP/PS1 mice with oral vaccination, accompanied by elevation of complement factors C1q and C3 levels in the brain. Our results indicate that autophagy is closely involved in oral vaccination-induced A beta clearance, and modulating the autophagy pathway may be an important strategy for AD prevention and intervention.
引用
收藏
页码:491 / 504
页数:14
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