Porcine Circovirus Type 2 Induces Autophagy via the AMPK/ERK/TSC2/mTOR Signaling Pathway in PK-15 Cells

被引:79
作者
Zhu, Binglin [1 ,2 ]
Zhou, Yingshan [1 ,2 ]
Xu, Fei [1 ,2 ]
Shuai, Jiangbing [3 ]
Li, Xiaoliang [1 ,2 ]
Fang, Weihuan [1 ,2 ]
机构
[1] Zhejiang Univ, Inst Prevent Vet Med, Zhejiang Prov Key Lab Prevent Vet Med, Hangzhou 310003, Zhejiang, Peoples R China
[2] Zhejiang Univ, Minist Educ, Key Lab Mol Anim Nutr, Hangzhou 310003, Zhejiang, Peoples R China
[3] Zhejiang Entry Exit Inspect & Quarantine Bur, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
HEPATITIS-C VIRUS; ACTIVATED PROTEIN-KINASE; NF-KAPPA-B; TUBEROUS SCLEROSIS; TRIGGERS AUTOPHAGY; REPLICATION; ERK; PHOSPHORYLATION; AMPK; MACHINERY;
D O I
10.1128/JVI.01434-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porcine circovirus type 2 (PCV2) uses autophagy machinery to enhance its replication in PK-15 cells. However, the underlying mechanisms are unknown. By the use of specific inhibitors, RNA interference, and coimmunoprecipitation, we show that PCV2 induces autophagy in PK-15 cells through a pathway involving the kinases AMP-activated protein kinase (AMPK) and extracellular signal-regulated kinase 1/2 (ERK1/2), the tumor suppressor protein TSC2, and the mammalian target of rapamycin (mTOR). AMPK and ERK1/2 positively regulate autophagy through negative control of the mTOR pathway by phosphorylating TSC2 in PCV2-infected PK-15 cells. Thus, PCV2 might induce autophagy via the AMPK/ERK/TSC2/mTOR signaling pathway in the host cells, representing a pivotal mechanism for PCV2 pathogenesis.
引用
收藏
页码:12003 / 12012
页数:10
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