• 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

小鼠肝炎病毒A59株从不同上皮细胞类型的相对面释放。

Mouse hepatitis virus strain A59 is released from opposite sides of different epithelial cell types.

作者信息

Rossen J W, Strous G J, Horzinek M C, Rottier P J

机构信息

Department of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht University, The Netherlands.

出版信息

J Gen Virol. 1997 Jan;78 ( Pt 1):61-9. doi: 10.1099/0022-1317-78-1-61.

DOI:10.1099/0022-1317-78-1-61
PMID:9010286
Abstract

Coronaviruses infect humans and animals through epithelial cells of the gastrointestinal and respiratory tracts that serve as their primary target. When studying infections in cultured polarized epithelial cells, we found previously that coronaviruses are released from specific plasma-membrane domains; thus, mouse hepatitis virus (strain A59; MHV-A59) leaves murine epithelial kidney cells from the basolateral surface, whereas release of transmissible gastroenteritis virus from porcine epithelial kidney cells is confined to the apical membrane. This observation begged the question whether a particular coronavirus is consistently shed through the same membrane, irrespective of the nature of the epithelial cell. We therefore extended our studies with MHV-A59 to Madin-Darby canine kidney (MDCK) strain I and human colon carcinoma (Caco-2) cells, both of which are naturally refractory to MHV-A59 but were made susceptible to infection by transfection with recombinant MHV receptor cDNA. The release of MHV-A59 from Caco(MHVR) cells occurred preferentially from the basolateral side, consistent with our previous observations. In contrast, release from MDCK(MHVR) cells occurred almost exclusively from the apical surface. Because of this difference, we studied MHV-A59 infection of MDCK(MHVR) cells in more detail. The virus entered the cells preferentially from the apical side, a situation similar to that in murine epithelial cells, where the highest density of MHV receptor glycoprotein was found. The results from this and previous studies show that targeting of vesicles containing MHV-A59 to a specific side of epithelial cells may vary in different epithelial cell types.

摘要

冠状病毒通过作为其主要靶标的胃肠道和呼吸道上皮细胞感染人类和动物。在研究培养的极化上皮细胞中的感染时,我们之前发现冠状病毒从特定的质膜结构域释放;因此,小鼠肝炎病毒(A59株;MHV - A59)从鼠肾上皮细胞的基底外侧表面离开,而传染性胃肠炎病毒从猪肾上皮细胞的释放局限于顶端膜。这一观察结果引发了一个问题,即特定的冠状病毒是否无论上皮细胞的性质如何,都始终通过同一膜释放。因此,我们将对MHV - A59的研究扩展到了麦迪逊 - 达比犬肾(MDCK)I株和人结肠癌细胞(Caco - 2),这两种细胞对MHV - A59天然具有抗性,但通过转染重组MHV受体cDNA使其易受感染。MHV - A59从Caco(MHVR)细胞的释放优先发生在基底外侧,这与我们之前的观察结果一致。相比之下,从MDCK(MHVR)细胞的释放几乎完全发生在顶端表面。由于这种差异,我们更详细地研究了MHV - A59对MDCK(MHVR)细胞的感染。病毒优先从顶端进入细胞,这种情况类似于在鼠上皮细胞中发现的情况,在鼠上皮细胞中发现了最高密度的MHV受体糖蛋白。这项研究和之前研究的结果表明,含有MHV - A59的囊泡靶向到上皮细胞特定一侧的情况在不同的上皮细胞类型中可能有所不同。

相似文献

1
Mouse hepatitis virus strain A59 is released from opposite sides of different epithelial cell types.小鼠肝炎病毒A59株从不同上皮细胞类型的相对面释放。
J Gen Virol. 1997 Jan;78 ( Pt 1):61-9. doi: 10.1099/0022-1317-78-1-61.
2
Coronaviruses in polarized epithelial cells.极化上皮细胞中的冠状病毒。
Adv Exp Med Biol. 1995;380:135-8. doi: 10.1007/978-1-4615-1899-0_22.
3
The viral spike protein is not involved in the polarized sorting of coronaviruses in epithelial cells.病毒刺突蛋白不参与冠状病毒在上皮细胞中的极性分选。
J Virol. 1998 Jan;72(1):497-503. doi: 10.1128/JVI.72.1.497-503.1998.
4
The murine coronavirus mouse hepatitis virus strain A59 from persistently infected murine cells exhibits an extended host range.来自持续感染小鼠细胞的鼠冠状病毒A59株表现出扩大的宿主范围。
J Virol. 1997 Dec;71(12):9499-507. doi: 10.1128/JVI.71.12.9499-9507.1997.
5
Selection in persistently infected murine cells of an MHV-A59 variant with extended host range.在持续感染的鼠细胞中筛选具有扩大宿主范围的MHV - A59变体。
Adv Exp Med Biol. 1998;440:735-41. doi: 10.1007/978-1-4615-5331-1_95.
6
MHV-A59 enters polarized murine epithelial cells through the apical surface but is released basolaterally.MHV - A59通过顶端表面进入极化的小鼠上皮细胞,但从基底外侧释放。
Virology. 1995 Jun 20;210(1):54-66. doi: 10.1006/viro.1995.1316.
7
A murine and a porcine coronavirus are released from opposite surfaces of the same epithelial cells.一种鼠冠状病毒和一种猪冠状病毒从同一上皮细胞的相对表面释放出来。
Virology. 1996 Oct 1;224(1):345-51. doi: 10.1006/viro.1996.0540.
8
Persistent infection of cultured cells with mouse hepatitis virus (MHV) results from the epigenetic expression of the MHV receptor.小鼠肝炎病毒(MHV)对培养细胞的持续感染源于MHV受体的表观遗传表达。
J Virol. 1995 Sep;69(9):5535-43. doi: 10.1128/JVI.69.9.5535-5543.1995.
9
Several members of the mouse carcinoembryonic antigen-related glycoprotein family are functional receptors for the coronavirus mouse hepatitis virus-A59.小鼠癌胚抗原相关糖蛋白家族的几个成员是冠状病毒小鼠肝炎病毒A59的功能性受体。
J Virol. 1993 Jan;67(1):1-8. doi: 10.1128/JVI.67.1.1-8.1993.
10
Purified, soluble recombinant mouse hepatitis virus receptor, Bgp1(b), and Bgp2 murine coronavirus receptors differ in mouse hepatitis virus binding and neutralizing activities.纯化的可溶性重组小鼠肝炎病毒受体Bgp1(b)和Bgp2鼠冠状病毒受体在小鼠肝炎病毒结合和中和活性方面存在差异。
J Virol. 1998 Sep;72(9):7237-44. doi: 10.1128/JVI.72.9.7237-7244.1998.

引用本文的文献

1
Preferential apical infection of Caco-2 intestinal cell monolayers by SARS-CoV-2 is associated with damage to cellular barrier integrity: Implications for the pathophysiology of COVID-19.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)对Caco-2肠细胞单层的优先顶端感染与细胞屏障完整性受损有关:对2019冠状病毒病病理生理学的启示。
PLoS One. 2025 Feb 10;20(2):e0313068. doi: 10.1371/journal.pone.0313068. eCollection 2025.
2
Endocytosis and Transcytosis of SARS-CoV-2 Across the Intestinal Epithelium and Other Tissue Barriers.SARS-CoV-2 经肠道上皮和其他组织屏障的内吞作用和转胞吞作用。
Front Immunol. 2021 Sep 7;12:636966. doi: 10.3389/fimmu.2021.636966. eCollection 2021.
3
Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells.
从肾小管上皮细胞中释放致病性旧世界汉坦病毒。
Virol J. 2012 Nov 30;9:299. doi: 10.1186/1743-422X-9-299.
4
Transmissible gastroenteritis virus (TGEV)-based vectors with engineered murine tropism express the rotavirus VP7 protein and immunize mice against rotavirus.基于传染性胃肠炎病毒(TGEV)的工程化鼠嗜性载体表达轮状病毒 VP7 蛋白,并可使小鼠对轮状病毒产生免疫。
Virology. 2011 Feb 5;410(1):107-18. doi: 10.1016/j.virol.2010.10.036. Epub 2010 Nov 21.
5
Mouse hepatitis coronavirus RNA replication depends on GBF1-mediated ARF1 activation.小鼠肝炎冠状病毒RNA复制依赖于GBF1介导的ARF1激活。
PLoS Pathog. 2008 Jun 13;4(6):e1000088. doi: 10.1371/journal.ppat.1000088.
6
Cyclooxygenase activity is important for efficient replication of mouse hepatitis virus at an early stage of infection.环氧化酶活性对于小鼠肝炎病毒在感染早期的有效复制很重要。
Virol J. 2007 Jun 7;4:55. doi: 10.1186/1743-422X-4-55.
7
Entry of viruses through the epithelial barrier: pathogenic trickery.病毒通过上皮屏障的进入:致病的伎俩。
Nat Rev Mol Cell Biol. 2003 Jan;4(1):57-68. doi: 10.1038/nrm1005.
8
Sorting of Marburg virus surface protein and virus release take place at opposite surfaces of infected polarized epithelial cells.马尔堡病毒表面蛋白的分选和病毒释放发生在受感染的极化上皮细胞的相对表面。
J Virol. 2001 Feb;75(3):1274-83. doi: 10.1128/JVI.75.3.1274-1283.2001.
9
Human coronavirus 229E infects polarized airway epithelia from the apical surface.人冠状病毒229E从顶端表面感染极化的气道上皮细胞。
J Virol. 2000 Oct;74(19):9234-9. doi: 10.1128/jvi.74.19.9234-9239.2000.
10
The viral spike protein is not involved in the polarized sorting of coronaviruses in epithelial cells.病毒刺突蛋白不参与冠状病毒在上皮细胞中的极性分选。
J Virol. 1998 Jan;72(1):497-503. doi: 10.1128/JVI.72.1.497-503.1998.