具有不同p30肽图的Moloney小鼠白血病病毒变体与不同临床类型的白血病相关

Birgitta Åsjö , Elena Buetti , Eva-Maria Fenyö , Heidi Diggelmann , George Klein
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引用次数: 3

摘要

新生儿接种莫洛尼MuLV (M-MuLV)后引起的小鼠白血病主要有两种类型。一种以脾脏和淋巴结肿大为特征,具有正常的二倍体核型。胸腺肿大是第二类最显著的特征,累及或不累及脾脏。大约一半的胸腺瘤是三体的,有一条额外的15号染色体。从两种白血病中分离的c型病毒在p30肽图上存在差异。从接种了mulv的4周大的新生小鼠白血病前期组织中分离出的p30是“胸腺”型或“脾”型。这些结果表明,这两种病毒类型已经存在于最初的接种物中,并在不同的组织中安家。相应的gp70分子的肽图显示没有器官相关的模式:每个病毒分离物都有不同的gp70谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Moloney murine leukemia virus variants with distinct p30 peptide maps are associated with different clinical types of leukemia

Mouse leukemias arising after neonatal inoculation of Moloney MuLV (M-MuLV) are of two main types. One is characterized by enlargement of spleen and lymph nodes, and has a normal diploid karyotype. Thymus enlargement is the most prominent feature of the second type, with or without spleen involvement. About half of the thymomas are trisomic with an extra chromosome 15. C-type viruses isolated from the two leukemia types differed with regard to their p30 peptide maps. The p30s isolated from the preleukemic tissues of a 4-weeks-old, neonatally MuLV-inoculated mouse were either of the ‘thymic’ or the ‘splenic’ type. These results suggest that the two virus types were already present in the original inoculum and had homed to different tissues. The peptide maps of the corresponding gp70 molecules showed no organ-related pattern: each virus isolate had a distinct gp70 profile.

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