›› 2007, Vol. 27 ›› Issue (2): 112-115.

• 论文 • 上一篇    下一篇

不同接种方法建立小鼠L1210白血病模型的比较研究

  

  1. 福建医科大学 1.实验动物中心;2.协和医院,福州 350004
  • 收稿日期:2006-09-04 出版日期:2007-02-28 发布日期:2007-02-28
  • 基金资助:
    福建省科技厅科研项目(2004Y014)资助

Comparative study on Mouse L1210 Leukemia Model Established by Different Ways

  1. 1. Animal Experimental Center, 2. Department of Hematology,Xiehe Hospital, Fujian Medical University, Fuzhou 350001, China
  • Received:2006-09-04 Online:2007-02-28 Published:2007-02-28

摘要: 目的 探讨不同接种方式制备的小鼠白血病模型的生物学特性.方法 常规培养小鼠急性淋巴细胞白血病细胞系L1210,调整浓度至1×107个/ml,每只DBA/2小鼠注射细胞悬液0.1 ml,分别给以静脉、皮下及腹腔注射.观察小鼠成瘤情况,定期计数各组小鼠外周白细胞数量及观察细胞形态改变,取濒死小鼠的肝、脾、肺、肾等脏器称重并制作病理切片.结果 各组小鼠成瘤率均为100%,成瘤天数分别为:14、7和14d;平均存活天数分别为:24.4±3.05,24.8±1.79,18.8±1.79 d.接种后2周外周血白细胞数目分别增加至18.45±1.84、22.0±4.11、28.48±6.74 x 109/L,接种后3周外周血白细胞数目分别增加至22.31±12.08×109/L(A组)和68.18±2.82×109/L(B组);外周血涂片中均可见白血病细胞;各组濒死小鼠肝、脾有弥漫性白血病细胞浸润,主要为幼稚淋巴细胞,正常组织结构破坏,肺和肾内有少量白血病细胞浸润,正常组织结构破坏不明显,肺脏有明显出血.结论 静脉、皮下、腹腔注射体外培养的L1210细胞于DBA/2小鼠构建肿瘤动物模型的方法均是可行的方式,各种方法有不同的生物学特性和优缺点,可根据研究目的的不同,选用不同的接种方式.

关键词: 白血病细胞, 成瘤性, 动物模型, 接种方式

Abstract: Objective To investigate biologic characters of a mouse leukemia model prepared by different ways. Methods The mouse acute lymphoblastic leukemia cell line L1210 was conventionally cultured and modulated into 1 xl07/ml. 0.1ml cell suspension was infused into every DBA/2 mouse by vena caudalis (A group), sub cutis (B group) and abdominal cavity (C group) respectively. The formation of leukemia in mouse was investigated. The amount of peripheric leucocyte in mouse blood was counted and the morphological changes were detected timely. The liver, spleen, kidney and lung of the dying mouse were kept,weighed and maken into pathological sections. Results The ratio of tumor formation was 100% in all groups, which spent 14,7 and 14 days respectively. The average survival days of the three groups were 24.4士3.05,24.8士1.79 and 18.8±1,79d days. The amount of peripheric leucocyte increased remarkably after infusion, which was (18.45±1.84)xl09/L、(22.0±4.11) × 109/L and (28.48±6.74)×l09/Ltwo weeks later and (22.31±12.08)×l09/L (A group) and (68.18±2.82)× 109/L (B group) three weeks later. Leukemic cells could be found on peripheral blood smears. In pathological sections of the dying mouse’ liver and spleen, infused leukemic cell infiltration, mainly immature lymphocytes, could be found, accompanied with destroy of normal tissue and structure. A small quantity of leukemic cells were found in lung and kidney, destroy of their normal tissue and structure was not obviously and hemorrhage appeared in lung obviously. Conclusions Inoculation of LI 210 cells into DBA/2 mouse by vena caudalis,subcutis and abdominal cavity was feasible to prepare a mouse leukemia model. There were different biological characters, merits and defects in the model due to the different infusion ways. A certain infusion way should be selected according to the aims of the research.

Key words: Leukemic cell, Tumor formation, Animal model, Infusion way