• 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

小鼠细小病毒(MVMi)对造血干细胞和定向祖细胞的体外骨髓抑制作用。

In vitro myelosuppressive effects of the parvovirus minute virus of mice (MVMi) on hematopoietic stem and committed progenitor cells.

作者信息

Segovia J C, Real A, Bueren J A, Almendral J M

机构信息

Unidad de Biología Celular y Molecular, CIEMAT, Madrid, Spain.

出版信息

Blood. 1991 Mar 1;77(5):980-8.

PMID:1847313
Abstract

The interaction of two strains of the parvovirus minute virus of mice (MVM) with the mouse hematopoietic system has been studied. The immunosuppressive strain MVMi, but not the prototype virus MVMp, inhibited hematopoiesis in vitro, as judged by colony-forming assays of the erythroid burst-forming unit and granulocyte-monocyte colony-forming unit (CFU-GM) progenitors. Interestingly, primitive hematopoietic cells of the stem compartment (CFU-S12d), were equally susceptible to the MVMi cytotoxic infection, unravelling an unprecedented feature of virus-hematopoiesis interactions. The replication of both strains of MVM virus was evaluated in primary myeloid cells of long-term bone marrow cultures. A high viral DNA synthesis and maturation was observed in MVMi-infected myeloid cells, but it was undetectable in MVMp infections; moreover, the expression of the cytotoxic nonstructural NS-1 protein, a more reliable parameter of cell permissiveness to MVM infection, was only detected in MVMi-infected cells. Correspondingly, MVMi was propagated to high titers of infectious virus and it mediated an acute myelosuppression in these cultures. We conclude that MVMi has a wider tropism than was previously suspected and it is proposed that cytotoxic infection of hematopoietic stem cells, besides that of committed progenitors, may provide an additional basis to understand the pathogenesis of certain animal and human bone marrow failures of viral etiology.

摘要

已经研究了两株小鼠细小病毒(MVM)与小鼠造血系统的相互作用。通过对红系爆式集落形成单位和粒细胞-单核细胞集落形成单位(CFU-GM)祖细胞进行集落形成分析判断,免疫抑制性毒株MVMi而非原型病毒MVMp在体外抑制造血作用。有趣的是,干细胞区室的原始造血细胞(CFU-S12d)对MVMi细胞毒性感染同样敏感,这揭示了病毒与造血相互作用的一个前所未有的特征。在长期骨髓培养的原代髓系细胞中评估了两株MVM病毒的复制情况。在感染MVMi的髓系细胞中观察到高水平的病毒DNA合成和成熟,但在MVMp感染中未检测到;此外,细胞毒性非结构NS-1蛋白的表达是细胞对MVM感染易感性的一个更可靠参数,仅在感染MVMi的细胞中检测到。相应地,MVMi能繁殖至高滴度的感染性病毒,并在这些培养物中介导急性骨髓抑制。我们得出结论,MVMi的嗜性比之前怀疑的更广,并且提出除了定向祖细胞外,造血干细胞的细胞毒性感染可能为理解某些病毒病因导致的动物和人类骨髓衰竭的发病机制提供额外依据。

相似文献

1
In vitro myelosuppressive effects of the parvovirus minute virus of mice (MVMi) on hematopoietic stem and committed progenitor cells.小鼠细小病毒(MVMi)对造血干细胞和定向祖细胞的体外骨髓抑制作用。
Blood. 1991 Mar 1;77(5):980-8.
2
Cytotoxic infection of hematopoietic stem and committed progenitor cells by the parvovirus minute virus of mice. Propagation of an acute myelosuppression in culture.小鼠细小病毒对造血干细胞和定向祖细胞的细胞毒性感染。培养中急性骨髓抑制的传播。
Ann N Y Acad Sci. 1991;628:262-72. doi: 10.1111/j.1749-6632.1991.tb17255.x.
3
The pathogenesis of infection with minute virus of mice depends on expression of the small nonstructural protein NS2 and on the genotype of the allotropic determinants VP1 and VP2.小鼠微小病毒感染的发病机制取决于小非结构蛋白NS2的表达以及同种异型决定簇VP1和VP2的基因型。
J Virol. 1992 May;66(5):3118-24. doi: 10.1128/JVI.66.5.3118-3124.1992.
4
Severe leukopenia and dysregulated erythropoiesis in SCID mice persistently infected with the parvovirus minute virus of mice.持续感染小鼠细小病毒的重症联合免疫缺陷(SCID)小鼠出现严重白细胞减少和红细胞生成失调。
J Virol. 1999 Mar;73(3):1774-84. doi: 10.1128/JVI.73.3.1774-1784.1999.
5
Parvovirus infection suppresses long-term repopulating hematopoietic stem cells.细小病毒感染会抑制长期重建造血干细胞。
J Virol. 2003 Aug;77(15):8495-503. doi: 10.1128/jvi.77.15.8495-8503.2003.
6
In vitro and in vivo susceptibility of mouse megakaryocytic progenitors to strain i of parvovirus minute virus of mice.小鼠巨核细胞祖细胞对小鼠细小病毒I株的体外和体内敏感性
Exp Hematol. 2001 Nov;29(11):1303-9. doi: 10.1016/s0301-472x(01)00724-x.
7
Myeloid depression follows infection of susceptible newborn mice with the parvovirus minute virus of mice (strain i).用小鼠细小病毒(i株)感染易感新生小鼠后会出现骨髓抑制。
J Virol. 1995 May;69(5):3229-32. doi: 10.1128/JVI.69.5.3229-3232.1995.
8
Genome replication and postencapsidation functions mapping to the nonstructural gene restrict the host range of a murine parvovirus in human cells.定位于非结构基因的基因组复制和衣壳化后功能限制了鼠细小病毒在人细胞中的宿主范围。
J Virol. 2001 Dec;75(23):11573-82. doi: 10.1128/JVI.75.23.11573-11582.2001.
9
Replication of B19 parvovirus in highly enriched hematopoietic progenitor cells from normal human bone marrow.B19细小病毒在来自正常人骨髓的高度富集造血祖细胞中的复制。
J Virol. 1988 Aug;62(8):3059-63. doi: 10.1128/JVI.62.8.3059-3063.1988.
10
Parvovirus minute virus of mice strain i multiplication and pathogenesis in the newborn mouse brain are restricted to proliferative areas and to migratory cerebellar young neurons.小鼠细小病毒i株在新生小鼠脑中的增殖和发病机制局限于增殖区域和迁移中的小脑年轻神经元。
J Virol. 1996 Nov;70(11):8109-16. doi: 10.1128/JVI.70.11.8109-8116.1996.

引用本文的文献

1
Antiangiogenic Vascular Endothelial Growth Factor-Blocking Peptides Displayed on the Capsid of an Infectious Oncolytic Parvovirus: Assembly and Immune Interactions.血管内皮生长因子拮抗肽在传染性溶瘤细小病毒衣壳上的展示:组装和免疫相互作用。
J Virol. 2019 Sep 12;93(19). doi: 10.1128/JVI.00798-19. Print 2019 Oct 1.
2
A field strain of minute virus of mice (MVMm) exhibits age- and strain-specific pathogenesis.一种野毒株微小病毒鼠(MVMm)表现出与年龄和株有关的发病机制。
J Gen Virol. 2018 Apr;99(4):558-566. doi: 10.1099/jgv.0.001044. Epub 2018 Mar 8.
3
Late Maturation Steps Preceding Selective Nuclear Export and Egress of Progeny Parvovirus.
子代细小病毒选择性核输出和释放之前的后期成熟步骤。
J Virol. 2016 May 12;90(11):5462-74. doi: 10.1128/JVI.02967-15. Print 2016 Jun 1.
4
Persistent viremia by a novel parvovirus in a slow loris (Nycticebus coucang) with diffuse histiocytic sarcoma.一只患有弥漫性组织细胞肉瘤的懒猴(懒猴属)感染新型细小病毒后出现持续性病毒血症。
Front Microbiol. 2014 Dec 1;5:655. doi: 10.3389/fmicb.2014.00655. eCollection 2014.
5
Experimental infection of mice with hamster parvovirus: evidence for interspecies transmission of mouse parvovirus 3.用仓鼠细小病毒对小鼠进行实验性感染:小鼠细小病毒3种间传播的证据
Comp Med. 2010 Apr;60(2):123-9.
6
Principles of bone marrow transplantation (BMT): providing optimal veterinary and husbandry care to irradiated mice in BMT studies.骨髓移植(BMT)的原则:在BMT研究中为受辐照小鼠提供最佳的兽医和饲养护理。
J Am Assoc Lab Anim Sci. 2009 Jan;48(1):11-22.
7
Minute virus of mice: antibody response, viral shedding, and persistence of viral DNA in multiple strains of mice.小鼠微小病毒:多种品系小鼠的抗体反应、病毒排泄及病毒DNA的持续存在
Comp Med. 2008 Aug;58(4):360-8.
8
Differential susceptibility of C57BL/6NCr and B6.Cg-Ptprca mice to commensal bacteria after whole body irradiation in translational bone marrow transplant studies.在转化性骨髓移植研究中,C57BL/6NCr和B6.Cg-Ptprca小鼠在全身照射后对共生细菌的易感性差异。
J Transl Med. 2008 Feb 28;6:10. doi: 10.1186/1479-5876-6-10.
9
Evolution to pathogenicity of the parvovirus minute virus of mice in immunodeficient mice involves genetic heterogeneity at the capsid domain that determines tropism.小鼠细小病毒在免疫缺陷小鼠中向致病性的演变涉及衣壳结构域的基因异质性,该结构域决定了嗜性。
J Virol. 2008 Feb;82(3):1195-203. doi: 10.1128/JVI.01692-07. Epub 2007 Nov 28.
10
Minute virus of mice, a parvovirus, in complex with the Fab fragment of a neutralizing monoclonal antibody.小鼠微小病毒,一种细小病毒,与一种中和性单克隆抗体的Fab片段形成复合物。
J Virol. 2007 Sep;81(18):9851-8. doi: 10.1128/JVI.00775-07. Epub 2007 Jul 11.