Slavin S, Weiss L, Morecki S, Bassat H B, Leizerowitz R, Gamliel H, Korkesh A, Voss R, Polliack A
Cancer Res. 1981 Oct;41(10):4162-6.
A murine model of a spontaneous, transplantable BALB/c B-cell leukemia (BCL1) is described. Extreme leukemia and splenomegaly develop in H-2d-compatible recipients of tumor cells. Tumor cells are medium to large lymphocytes that can be transformed into plasmacytoid cells following in vitro stimulation with lipopolysaccharide. Karyotypic analysis of transformed tumor cells reveals 36 chromosomes with several monosomies and 7 markers chromosomes. The ultrastructure of the tumor cells was studied using transmission and scanning electron microscopy. Although the appearance of tumor cells seems normal by morphological criteria, an impaired capping ability was documented using the fluorescein-conjugated concanavalin A-binding test. Impaired capping ability was documented before leukemia was overt as early as 1 to 3 days following inoculation of tumor cells. The B-cell leukemia (BCL1) provides a useful murine model for the study of various aspects of human bone marrow-derived malignant disorders.
本文描述了一种自发性、可移植的BALB/c B细胞白血病(BCL1)小鼠模型。在与肿瘤细胞H-2d兼容的受体中会出现严重的白血病和脾肿大。肿瘤细胞为中到大淋巴细胞,经脂多糖体外刺激后可转化为浆细胞样细胞。对转化后的肿瘤细胞进行核型分析,发现有36条染色体,存在多个单体和7条标记染色体。使用透射电子显微镜和扫描电子显微镜对肿瘤细胞的超微结构进行了研究。尽管从形态学标准来看肿瘤细胞的外观似乎正常,但通过荧光素偶联刀豆球蛋白A结合试验证明其帽化能力受损。早在接种肿瘤细胞后1至3天白血病明显出现之前,就已证明帽化能力受损。B细胞白血病(BCL1)为研究人类骨髓源性恶性疾病的各个方面提供了一种有用的小鼠模型。