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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。

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