van den Akker T W, Radl J, Franken-Postma E, Hagemeijer A
Department of Immunology, Erasmus University Rotterdam, The Netherlands.
Cancer Genet Cytogenet. 1996 Feb;86(2):156-61. doi: 10.1016/0165-4608(95)00169-7.
Multiple myeloma (MM) and Waldenstrom's macroglobulinemia-like lymphoma (MW) appear spontaneously in C57BL/KaLwRij mice at a frequency of 0.5% and 0.2%, respectively. They can readily be propagated by intravenous transfer of mainly bone marrow or spleen cells into syngeneic recipients. Previous studies demonstrated that these mouse malignant monoclonal gammopathies (MMG) show clinical and biologic features that closely resemble those of the corresponding human diseases and thus could be used as experimental models. We report on cytogenetic analysis of two mouse MW and five MM in vivo cell lines of the 5TMM series propagated in syngeneic mice. These studies demonstrated clonal abnormalities in all cell lines, hyperdiploid karyotype in both MW and one MM lines, and hypotriploidy, hypertriploidy, or hypotetraploidy in the other lines. Structural abnormalities of chromosome 15 were observed in all MM lines. In five MM lines, frequent rearrangements were also found for chromosome numbers 1, 2, 5, and 12. A single chromosomal abnormality, as found in induced mouse plasmacytomas and resembling Burkitt lymphoma, was not found in mouse MM and MW. It was concluded that spontaneously originating C57BL MM of the 5T series is a better model for human MM than pristane-induced BALB/c or NZB plasmacytoma.
多发性骨髓瘤(MM)和瓦尔登斯特伦巨球蛋白血症样淋巴瘤(MW)分别以0.5%和0.2%的频率自发出现于C57BL/KaLwRij小鼠中。通过将主要是骨髓或脾细胞静脉内转移至同基因受体,它们能够很容易地进行传代。先前的研究表明,这些小鼠恶性单克隆丙种球蛋白病(MMG)表现出与相应人类疾病极为相似的临床和生物学特征,因此可作为实验模型。我们报告了对在同基因小鼠中传代的5TMM系列的两株小鼠MW和五株MM体内细胞系进行的细胞遗传学分析。这些研究表明,所有细胞系均存在克隆异常,MW和一株MM系为超二倍体核型,其他系为亚三倍体、超三倍体或亚四倍体。在所有MM系中均观察到15号染色体的结构异常。在五株MM系中,还发现1、2、5和12号染色体频繁重排。在小鼠MM和MW中未发现如在诱导的小鼠浆细胞瘤中所见且类似于伯基特淋巴瘤的单一染色体异常。得出的结论是,5T系列自发产生的C57BL MM比 pristane诱导的BALB/c或NZB浆细胞瘤更适合作为人类MM的模型。