• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

乙型肝炎病毒的进入、组装和释放。

Hepatitis B virus entry, assembly, and egress.

作者信息

Chuang Yu-Chen, Ou J-H James

机构信息

Department of Molecular Microbiology and Immunology, University of Southern California Keck School of Medicine, Los Angeles, California, USA.

出版信息

Microbiol Mol Biol Rev. 2024 Dec 18;88(4):e0001424. doi: 10.1128/mmbr.00014-24. Epub 2024 Oct 23.

DOI:10.1128/mmbr.00014-24
PMID:39440957
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11653734/
Abstract

SUMMARYHepatitis B virus (HBV) is an important human pathogen that chronically infects approximately 250 million people in the world, resulting in ~1 million deaths annually. This virus is a hepatotropic virus and can cause severe liver diseases including cirrhosis and hepatocellular carcinoma. The entry of HBV into hepatocytes is initiated by the interaction of its envelope proteins with its receptors. This is followed by the delivery of the viral nucleocapsid to the nucleus for the release of its genomic DNA and the transcription of viral RNAs. The assembly of the viral capsid particles may then take place in the nucleus or the cytoplasm and may involve cellular membranes. This is followed by the egress of the virus from infected cells. In recent years, significant research progresses had been made toward understanding the entry, the assembly, and the egress of HBV particles. In this review, we discuss the molecular pathways of these processes and compare them with those used by hepatitis delta virus and hepatitis C virus , two other hepatotropic viruses that are also enveloped. The understanding of these processes will help us to understand how HBV replicates and causes diseases, which will help to improve the treatments for HBV patients.

摘要

摘要

乙型肝炎病毒(HBV)是一种重要的人类病原体,全球约有2.5亿人长期感染该病毒,每年导致约100万人死亡。这种病毒是嗜肝病毒,可引起包括肝硬化和肝细胞癌在内的严重肝脏疾病。HBV进入肝细胞是由其包膜蛋白与受体相互作用引发的。随后,病毒核衣壳被递送至细胞核以释放其基因组DNA并转录病毒RNA。病毒衣壳颗粒的组装可能在细胞核或细胞质中进行,且可能涉及细胞膜。随后病毒从受感染细胞中释放出来。近年来,在了解HBV颗粒的进入、组装和释放方面取得了重大研究进展。在本综述中,我们讨论这些过程的分子途径,并将它们与丁型肝炎病毒和丙型肝炎病毒(另外两种包膜嗜肝病毒)所使用的途径进行比较。对这些过程的理解将有助于我们了解HBV如何复制并引发疾病,这将有助于改善对HBV患者的治疗。

相似文献

1
Hepatitis B virus entry, assembly, and egress.乙型肝炎病毒的进入、组装和释放。
Microbiol Mol Biol Rev. 2024 Dec 18;88(4):e0001424. doi: 10.1128/mmbr.00014-24. Epub 2024 Oct 23.
2
NIH Consensus Statement on Management of Hepatitis C: 2002.美国国立卫生研究院关于丙型肝炎管理的共识声明:2002年。
NIH Consens State Sci Statements. 2002;19(3):1-46.
3
Asymmetric Modification of Hepatitis B Virus (HBV) Genomes by an Endogenous Cytidine Deaminase inside HBV Cores Informs a Model of Reverse Transcription.内源性胞嘧啶脱氨酶在乙型肝炎病毒核心内对乙型肝炎病毒(HBV)基因组进行不对称修饰,为逆转录模型提供了信息。
J Virol. 2018 Apr 27;92(10). doi: 10.1128/JVI.02190-17. Print 2018 May 15.
4
Therapeutic interventions aimed at cccDNA: unveiling mechanisms and evaluating the potency of natural products.针对cccDNA的治疗干预措施:揭示作用机制并评估天然产物的效力
Front Cell Infect Microbiol. 2025 Jun 17;15:1598872. doi: 10.3389/fcimb.2025.1598872. eCollection 2025.
5
Autographa californica multiple nucleopolyhedrovirus Ac51 interacts with Ac66 and facilitates its nuclear localization to promote the nuclear egress of nucleocapsids.苜蓿银纹夜蛾多核型多角体病毒Ac51与Ac66相互作用,并促进其核定位以促进核衣壳的核输出。
J Virol. 2025 Jun 17;99(6):e0196924. doi: 10.1128/jvi.01969-24. Epub 2025 May 28.
6
Surveillance of cirrhosis for hepatocellular carcinoma: systematic review and economic analysis.肝细胞癌肝硬化监测:系统评价与经济分析
Health Technol Assess. 2007 Sep;11(34):1-206. doi: 10.3310/hta11340.
7
The Lived Experience of Autistic Adults in Employment: A Systematic Search and Synthesis.成年自闭症患者的就业生活经历:系统检索与综述
Autism Adulthood. 2024 Dec 2;6(4):495-509. doi: 10.1089/aut.2022.0114. eCollection 2024 Dec.
8
Depalmitoylase ABHD16A negatively regulates the anti-hepatitis B virus activity of IFITM1.去棕榈酰化酶ABHD16A负向调节IFITM1的抗乙型肝炎病毒活性。
Microbiol Spectr. 2025 Jul;13(7):e0309524. doi: 10.1128/spectrum.03095-24. Epub 2025 May 28.
9
Signs and symptoms to determine if a patient presenting in primary care or hospital outpatient settings has COVID-19.在基层医疗机构或医院门诊环境中,如果患者出现以下症状和体征,可判断其是否患有 COVID-19。
Cochrane Database Syst Rev. 2022 May 20;5(5):CD013665. doi: 10.1002/14651858.CD013665.pub3.
10
Hepatitis B immunoglobulin during pregnancy for prevention of mother-to-child transmission of hepatitis B virus.孕期使用乙型肝炎免疫球蛋白预防乙肝病毒母婴传播。
Cochrane Database Syst Rev. 2017 Feb 11;2(2):CD008545. doi: 10.1002/14651858.CD008545.pub2.

引用本文的文献

1
Effects of cellular membranes and the precore protein on hepatitis B virus core particle assembly and DNA replication.细胞膜和前核心蛋白对乙型肝炎病毒核心颗粒组装及DNA复制的影响。
mBio. 2025 Apr 9;16(4):e0397224. doi: 10.1128/mbio.03972-24. Epub 2025 Mar 5.

本文引用的文献

1
Exosomes as Conduits: Facilitating Hepatitis B Virus-Independent Hepatitis D Virus Transmission and Propagation in Hepatocytes.外泌体作为载体:促进乙型肝炎病毒非依赖性丙型肝炎病毒在肝细胞中的传播和复制。
Viruses. 2024 May 22;16(6):825. doi: 10.3390/v16060825.
2
Treatment of Hepatitis D - A Future Role for Combination Therapy.丁型肝炎的治疗——联合疗法的未来作用
N Engl J Med. 2024 Jul 11;391(2):181-183. doi: 10.1056/NEJMe2406180. Epub 2024 Jun 6.
3
Exosomes target HBV-host interactions to remodel the hepatic immune microenvironment.外泌体靶向 HBV-宿主相互作用重塑肝脏免疫微环境。
J Nanobiotechnology. 2024 Jun 5;22(1):315. doi: 10.1186/s12951-024-02544-y.
4
Roles Played by DOCK11, a Guanine Nucleotide Exchange Factor, in HBV Entry and Persistence in Hepatocytes.DOCK11 作为鸟嘌呤核苷酸交换因子在 HBV 进入和在肝细胞中持续存在中的作用。
Viruses. 2024 May 8;16(5):745. doi: 10.3390/v16050745.
5
Hepatitis B surface antigen expression impairs endoplasmic reticulum stress-related autophagic flux by decreasing LAMP2.乙肝表面抗原表达通过降低溶酶体相关膜蛋白2(LAMP2)来损害内质网应激相关的自噬通量。
JHEP Rep. 2024 Jan 28;6(4):101012. doi: 10.1016/j.jhepr.2024.101012. eCollection 2024 Apr.
6
Hepatitis B virus RNAs co-opt ELAVL1 for stabilization and CRM1-dependent nuclear export.乙型肝炎病毒 RNA 劫持 ELAVL1 实现稳定,并通过 CRM1 依赖途径进行核输出。
PLoS Pathog. 2024 Feb 2;20(2):e1011999. doi: 10.1371/journal.ppat.1011999. eCollection 2024 Feb.
7
Structural basis for nuclear import of hepatitis B virus (HBV) nucleocapsid core.乙型肝炎病毒核衣壳核心的核输入的结构基础。
Sci Adv. 2024 Jan 12;10(2):eadi7606. doi: 10.1126/sciadv.adi7606. Epub 2024 Jan 10.
8
Conditional replication and secretion of hepatitis B virus genome uncover the truncated 3' terminus of encapsidated viral pregenomic RNA.条件复制和分泌乙型肝炎病毒基因组揭示了包裹的病毒前基因组 RNA 的截断 3'末端。
J Virol. 2023 Oct 31;97(10):e0076023. doi: 10.1128/jvi.00760-23. Epub 2023 Sep 27.
9
EGFR trafficking: effect of dimerization, dynamics, and mutation.表皮生长因子受体(EGFR)的转运:二聚化、动力学及突变的影响
Front Oncol. 2023 Sep 11;13:1258371. doi: 10.3389/fonc.2023.1258371. eCollection 2023.
10
Cellular Factors Involved in the Hepatitis D Virus Life Cycle.参与丁型肝炎病毒生命周期的细胞因子。
Viruses. 2023 Aug 3;15(8):1687. doi: 10.3390/v15081687.