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Porcine circovirus 3 capsid protein induces autophagy in HEK293T cells by inhibiting phosphorylation of the mammalian target of rapamycin.猪圆环病毒 3 衣壳蛋白通过抑制哺乳动物雷帕霉素靶蛋白的磷酸化诱导 HEK293T 细胞自噬。
J Zhejiang Univ Sci B. 2020 Jul;21(7):560-570. doi: 10.1631/jzus.B1900657.
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本文引用的文献

1
Porcine circovirus 3 Cap inhibits type I interferon signaling through interaction with STAT2.猪圆环病毒 3 衣壳蛋白通过与 STAT2 相互作用抑制 I 型干扰素信号通路。
Virus Res. 2020 Jan 2;275:197804. doi: 10.1016/j.virusres.2019.197804. Epub 2019 Nov 4.
2
Development and optimization of an intergeneric conjugation system and analysis of promoter activity in Streptomyces rimosus M527.开发和优化链霉菌属间杂交系统及分析棘孢小单孢菌 M527 启动子活性。
J Zhejiang Univ Sci B. 2019;20(11):891-900. doi: 10.1631/jzus.B1900270.
3
The Emerging Roles of mTORC1 in Macromanaging Autophagy.mTORC1在宏观调控自噬中的新作用
Cancers (Basel). 2019 Sep 24;11(10):1422. doi: 10.3390/cancers11101422.
4
Interactions between Autophagy and DNA Viruses.自噬与 DNA 病毒的相互作用。
Viruses. 2019 Aug 23;11(9):776. doi: 10.3390/v11090776.
5
Phosphorylation residue T175 in RsbR protein is required for efficient induction of sigma B factor and survival of Listeria monocytogenes under acidic stress.RsbR 蛋白中的磷酸化残基 T175 对于李斯特菌在酸性应激下有效诱导σB 因子和生存是必需的。
J Zhejiang Univ Sci B. 2019;20(8):660-669. doi: 10.1631/jzus.B1800551.
6
SIP/CacyBP promotes autophagy by regulating levels of BRUCE/Apollon, which stimulates LC3-I degradation.SIP/CacyBP 通过调节 BRUCE/Apollon 的水平来促进自噬,从而刺激 LC3-I 的降解。
Proc Natl Acad Sci U S A. 2019 Jul 2;116(27):13404-13413. doi: 10.1073/pnas.1901039116. Epub 2019 Jun 18.
7
The Role of Primary Cilia in the Crosstalk between the Ubiquitin⁻Proteasome System and Autophagy.原发性纤毛在泛素-蛋白酶体系统与自噬的串扰中的作用。
Cells. 2019 Mar 14;8(3):241. doi: 10.3390/cells8030241.
8
PCV2 replication promoted by oxidative stress is dependent on the regulation of autophagy on apoptosis.氧化应激促进 PCV2 复制依赖于自噬对细胞凋亡的调控。
Vet Res. 2019 Mar 5;50(1):19. doi: 10.1186/s13567-019-0637-z.
9
Induction of Porcine Dermatitis and Nephropathy Syndrome in Piglets by Infection with Porcine Circovirus Type 3.猪圆环病毒 3 型感染诱导仔猪皮炎肾病综合征。
J Virol. 2019 Feb 5;93(4). doi: 10.1128/JVI.02045-18. Print 2019 Feb 15.
10
First detection of porcine circovirus type 3 in Japan.日本首次检测到猪圆环病毒3型。
J Vet Med Sci. 2018 Sep 26;80(9):1468-1472. doi: 10.1292/jvms.18-0079. Epub 2018 Aug 6.

猪圆环病毒 3 衣壳蛋白通过抑制哺乳动物雷帕霉素靶蛋白的磷酸化诱导 HEK293T 细胞自噬。

Porcine circovirus 3 capsid protein induces autophagy in HEK293T cells by inhibiting phosphorylation of the mammalian target of rapamycin.

机构信息

Institute of Preventive Veterinary Medicine, Zhejiang University, Hangzhou 310058, China.

Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine, Hangzhou 310058, China.

出版信息

J Zhejiang Univ Sci B. 2020 Jul;21(7):560-570. doi: 10.1631/jzus.B1900657.

DOI:10.1631/jzus.B1900657
PMID:32633110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7383325/
Abstract

Porcine circovirus 3 (PCV3) has been detected in major pig-producing countries around the world since its first report in the US in 2016. Most current studies have focused on epidemiological investigations and detection methods of PCV3 because of lack of live virus strains for research on its pathogenesis in porcine cells or even in pigs. We constructed a recombinant plasmid pCMV-Cap carrying the PCV3 orf2 gene to investigate the effects of capsid (Cap) protein expression on autophagic response in human embryonic kidney cell line 293T (HEK293T). We demonstrate that PCV3 Cap protein induced complete autophagy shown as formation of autophagosomes and autophagosome-like vesicles as well as LC3-II conversion from LC3-I via inhibiting phosphorylation of the mammalian target of rapamycin (mTOR) in HEK293T cells. The ubiquitin-proteasome pathway is also involved in the autophagy process. These findings provide insight for further exploration of PCV3 pathogenetic mechanisms in porcine cells.

摘要

自 2016 年美国首次报道以来,猪圆环病毒 3 型(PCV3)已在世界主要养猪国家被检出。由于缺乏用于研究其在猪细胞甚至猪体内发病机制的活病毒株,目前大多数研究都集中在 PCV3 的流行病学调查和检测方法上。我们构建了携带 PCV3 orf2 基因的重组质粒 pCMV-Cap,以研究衣壳(Cap)蛋白表达对人胚肾细胞系 293T(HEK293T)自噬反应的影响。我们证明 PCV3 Cap 蛋白通过抑制哺乳动物雷帕霉素靶蛋白(mTOR)的磷酸化,诱导完全自噬,表现为自噬体和自噬体样小泡的形成以及 LC3-I 向 LC3-II 的转化。泛素-蛋白酶体途径也参与自噬过程。这些发现为进一步探索 PCV3 在猪细胞中的致病机制提供了思路。