Journal
MOLECULAR NEUROBIOLOGY
Volume 53, Issue 1, Pages 706-719Publisher
SPRINGER
DOI: 10.1007/s12035-014-9028-7
Keywords
Autophagy; MTOR; FBXW7; Persistent prion infection
Categories
Funding
- Chinese National Natural Science Foundation [81100980, 81101302, 31100117]
- China Mega-Project for Infectious Disease [2011ZX10004-101, 2012ZX10004215]
- SKLID Development Grant [2012SKLID102, 2011SKLID302, 2011SKLID204, 2011SKLID211]
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Autophagy is an important protein degradation pathway and a part of the innate immune system that is activated in the brain tissue during animal and human prion diseases. However, the possible mechanism by which prion infection triggers autophagy and the significance of activated autophagy on prion accumulation remain unknown. Here, we demonstrated that autophagic flux was enhanced in the persistent prion-infected cell line, SMB-S15. Knockdown of ATG5 and the presence of three autophagic inhibitors resulted in a significant increase of PrPSc. The mammalian target of rapamycin (MTOR) levels in SMB-S15 cells were also markedly decreased, in direct relation to PrPSc accumulation. F-box and WD repeat domain containing 7 (FBXW7) levels in SMB-S15 cells and in the brains of scrapie-agent 263K-infected hamsters were upregulated at the early stage of infection, leading to active ubiquitination and degradation of MTOR. Knockdown of FBXW7 in SMB-S15 cells remarkably inhibited autophagic flux and increased PrPSc accumulation. Thus, we conclude that prion infection induced the expression of FBXW7, which mediated MTOR ubiquitination and degradation, further altering phosphorylation status through cross talk between MTORC1 and AMPK and increasing autophagic flux. Autophagy may serve as innate immunity to degrade PrPSc and maintain prion homeostasis.
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