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由不同小鼠品系胚胎细胞化学激活的C型病毒引起的不同血液学疾病。

Different hematological diseases induced by type C viruses chemically activated from embryo cells of different mouse strains.

作者信息

Greenberger J S, Stephenson J R, Moloney W C, Aaronson S A

出版信息

Cancer Res. 1975 Jan;35(1):245-52.

PMID:45891
Abstract

Type C RNA viruses can be induced by certain chemicals from cells of many mouse strains. Both C58 and BALB/c cells have been shown to contain endogenous viruses that are designated N-tropic because they grow preferentially in cells of NIH Swiss mouse origin. While demonstrating many similar biological and immunological properties, the C58-induced virus is around 10-fold more infectious per physical particle than the N-tropic virus of BALB/c cells. In the present studies, inoculation of these viruses into newborn NIH Swiss mice led to the development of diseases associated with splenomegaly and lymphadenopathy at similar frequency in each group. The disease induced by C58-MuLV was histophathologically diagnosed as lymphoblastic leukemia and was highly malignant following transplantation into newborn mice. The histopathological appearance of spleens from BALB/c virus-affected animals was distinguishable, demonstrating instead myeloid metaplasia or myelogenous leukemia. These findings provide evidence that different endogenous mouse type C viruses can induce distinct diseases in the same mouse strain. Furthermore, they implicate the N-tropic virus endogenous to C58 cells as a major factor in the development of lymphoblastic leukemia that occurs at high frequency in that strain.

摘要

C型RNA病毒可由多种小鼠品系细胞中的某些化学物质诱导产生。C58和BALB/c细胞均已被证明含有内源性病毒,这些病毒被称为N趋向性病毒,因为它们优先在源自NIH瑞士小鼠的细胞中生长。虽然C58诱导的病毒和BALB/c细胞的N趋向性病毒表现出许多相似的生物学和免疫学特性,但就每个物理颗粒而言,C58诱导的病毒的感染性比BALB/c细胞的N趋向性病毒高约10倍。在本研究中,将这些病毒接种到新生的NIH瑞士小鼠体内,每组小鼠发生与脾肿大和淋巴结病相关疾病的频率相似。C58-MuLV诱导的疾病经组织病理学诊断为淋巴细胞白血病,移植到新生小鼠后具有高度恶性。受BALB/c病毒感染动物的脾脏组织病理学表现有所不同,表现为髓样化生或髓细胞性白血病。这些发现提供了证据,表明不同的内源性小鼠C型病毒可在同一小鼠品系中诱导不同的疾病。此外,这些发现表明C58细胞内的N趋向性病毒是该品系中高频发生的淋巴细胞白血病发展的主要因素。

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