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源自BALB/c的N型嗜亲性鼠白血病病毒的致病性

Pathogenicity of BALB/c-derived N-tropic murine leukemia viruses.

作者信息

Pedersen L, Strauss P G, Schmidt J, Luz A, Erfle V, Jørgensen P, Kjeldgaard N O, Pedersen F S

机构信息

Department of Molecular Biology and Plant Physiology, University of Aarhus, Denmark.

出版信息

Virology. 1990 Dec;179(2):931-5. doi: 10.1016/0042-6822(90)90171-m.

Abstract

N-tropic murine leukemia viruses have been observed in connection with radiation-induced osteosarcomagenesis in BALB/c mice. We have investigated the bone disease-inducing potential of molecularly cloned, BALB/c-derived N-tropic viruses in the random-bred NMRI mouse strain. The germ-line virus and an exogenous virus isolate were found to induce high incidences of osteopetrosis and lymphomas and a lower incidence of osteomas. Two viruses derived from somatically acquired proviruses of independent radiation-induced osteosarcomas induced lower incidence of osteopetrosis and lymphomas. Nucleotide sequence analysis of the long terminal repeat regions and RNase T1 fingerprint analysis revealed only few differences between the isolates. The possible involvement of N-tropic murine leukemia viruses in radiation-induced osteosarcomagenesis in the BALB/c mouse strain is discussed.

摘要

在BALB/c小鼠中,已观察到N-嗜性鼠白血病病毒与辐射诱导的骨肉瘤发生有关。我们研究了分子克隆的、源自BALB/c的N-嗜性病毒在随机繁殖的NMRI小鼠品系中诱导骨疾病的潜力。发现种系病毒和一种外源性病毒分离株可诱导高发性骨硬化症和淋巴瘤,以及较低发性骨瘤。两种源自独立辐射诱导骨肉瘤的体细胞获得性前病毒的病毒,诱导骨硬化症和淋巴瘤的发生率较低。对长末端重复区域的核苷酸序列分析和核糖核酸酶T1指纹分析显示,分离株之间只有很少的差异。讨论了N-嗜性鼠白血病病毒可能参与BALB/c小鼠品系辐射诱导的骨肉瘤发生。

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