[Acquisition of Primary Ph+ Bone Marrow Cells and Establishment of Ph+ B-ALL Mouse Model].

Q4 Medicine
Li Zhao, Dong-Hai Tang, Chun-Xiao Ren, Kai Zhao
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引用次数: 0

Abstract

Objective: To harvest the primary Philadelphia chromosome-positive (Ph+) cells of B-acute lymphoblastic leukemia (B-ALL) and to establish the B-ALL mouse model.

Methods: The plasmid carrying BCR-ABL P210 fusion gene was transferred into the bone marrow(BM) cells of C57BL/6J mice by retrovirus. Syngeneic mice irradiated with 9 Gy of 60Co γ-ray were injected with the transfected BM cells as the first generation (G1), and then the primary cells from the spleen and BM of the diseased mice were obtained and frozen. Sublethal γ-ray irradiated C57BL/6J mice were inoculated with the first generation of Ph+ cells for in vivo passage, which were named as the second generation (G2). The third and fourth generations (G3 and G4) of Ph+ cells and B-ALL mouse model were established by successive passages. Flow cytometry, H &E staining and peripheral blood smear were used to analyze the immunophenotypes and detect the pathological changes of the model mice.

Results: After infusion of P210-NGFR retrovirus infected BM cells, the mice exhibited significant symptoms including weight loss, lower limbs paralysis, and arched back. Primitive and immature lymphocytes were observed in peripheral blood smears of the leukemia mice. The results of H &E staining showed obvious infiltration of leukemic cells around the central vein of the hepatic lobule and at the edge of the liver in the diseased mice. The results of flow cytometry showed that the percentages of CD19+NGFR+ cells in spleen of the model mice were gradually increased with passage, which was 19.0%, 47.3% and 61.0% in G1, G2 and G3 mice, respectively. Immunophenotypic analysis indicated that Ph+ cells were stably passaged in B lymphocytes, and the purity of Ph+ B lymphocytes was obviously elevated with the increase of passage frequency.

Conclusion: In the present study, the primary Ph+ cells were successfully obtatined and passaged in vivo, and the B-ALL mouse model was successfully established.

[原代Ph+骨髓细胞的获取及Ph+ B-ALL小鼠模型的建立]。
目的:收集b -急性淋巴细胞白血病(B-ALL)原代费城染色体阳性(Ph+)细胞,建立B-ALL小鼠模型。方法:采用逆转录病毒法将携带BCR-ABL P210融合基因的质粒转染C57BL/6J小鼠骨髓细胞。用60Co γ射线照射9 Gy的同基因小鼠,注射转染后的BM细胞作为第一代(G1),然后从患病小鼠的脾脏和BM中获得原代细胞并冷冻。以亚致死γ射线照射C57BL/6J小鼠,接种第一代Ph+细胞进行体内传代,命名为第二代(G2)。连续传代建立第三代、第四代(G3、G4) Ph+细胞和B-ALL小鼠模型。采用流式细胞术、h&e染色及外周血涂片法分析模型小鼠的免疫表型及病理变化。结果:输注P210-NGFR逆转录病毒感染的BM细胞后,小鼠表现出体重减轻、下肢瘫痪和弓背等明显症状。白血病小鼠外周血涂片中可见原始淋巴细胞和未成熟淋巴细胞。h&e染色结果显示,病变小鼠肝小叶中心静脉周围及肝边缘有明显的白血病细胞浸润。流式细胞术结果显示,随着传代,模型小鼠脾脏中CD19+NGFR+细胞的百分比逐渐增加,G1、G2和G3小鼠分别为19.0%、47.3%和61.0%。免疫表型分析表明,Ph+细胞在B淋巴细胞中稳定传代,Ph+ B淋巴细胞纯度随传代次数的增加而明显升高。结论:本研究成功获得Ph+原代细胞并在体内传代,成功建立B-ALL小鼠模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
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