3-Anhydro-6-hydroxy-ophiobolin A, a fungal sesterterpene from Bipolaris oryzae induced autophagy and promoted the degradation of α-synuclein in PC12 cells

被引:20
作者
Xue, Danfeng [1 ,2 ]
Wang, Quanxin
Chen, Ziheng [1 ,2 ]
Cai, Lei [3 ]
Bao, Li [3 ]
Qi, Qiuyue [3 ]
Liu, Lei [2 ]
Wang, Xiaohui [1 ]
Jin, Haijing [1 ]
Wang, Jun [1 ]
Wu, Hao [1 ,2 ]
Liu, Hongwei [3 ]
Chen, Quan [1 ,2 ,4 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100101, Peoples R China
[3] Chinese Acad Sci, Inst Microbiol, State Key Lab Mycol, Beijing 100101, Peoples R China
[4] Nankai Univ, Coll Life Sci, Tianjin Key Lab Prot Sci, Tianjin 300071, Peoples R China
关键词
3-Anhydro-6-hydroxy-ophiobolin A; Autophagy; ROS; alpha-Synuclein; THERAPEUTIC TARGET; JNK1-MEDIATED PHOSPHORYLATION; PARKINSONS-DISEASE; APOPTOSIS; GROWTH; DEATH; OPHIOBOLIN; CLEARANCE; INDUCTION; PROTEINS;
D O I
10.1016/j.bmcl.2015.02.030
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Autophagy is defined as an evolutionarily conserved process responsible for degradation of the cytoplasmic components including protein aggregates via the lysosomal machinery. Increasing evidence has linked defective autophagic degradation of protein aggregates with the pathogenesis of neurodegenerative disorders, and it is suggested that promotion of autophagy is regarded as a potential therapeutic for these diseases including Parkinson's disease (PD). Here we identified, 3-anhydro-6-hydroxy-ophiobolin A (X15-2), an ophiobolin derivative from Bipolaris oryzae that can strongly induce autophagic degradation of alpha-synuclein, the major constituent of Lewy bodies. We showed that X15-2 induced autophagy is dependent on both Beclin1 and Beclin2. Knockout of ATG5 by CRISPER/Cas9 prevented X15-2 induced autophagy and degradation of alpha-synuclein. Mechanistically, we showed that X15-2 induces ROS and the activation of JNK signaling for the autophagic degradation of alpha-synuclein in PC12 cells. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1464 / 1470
页数:7
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