华西口腔医学杂志

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绿色荧光蛋白转染标记腺样囊性癌生长的裸鼠模型

陈正岗1 董作青1 张东1 周成军2 孙善珍3 刘少华1 魏奉才1   

  1. 1.山东大学齐鲁医院口腔颌面外科, 山东大学口腔医学研究所, 济南250012;2.山东大学第二医院病理科, 济南250033; 3.山东大学口腔医院病理科, 济南250012
  • 收稿日期:2011-08-25 修回日期:2011-08-25 出版日期:2011-08-20 发布日期:2011-08-20
  • 通讯作者: 刘少华,Tel:0531-82169247
  • 作者简介:陈正岗(1973—),男,山东人,主治医师,博士
  • 基金资助:

    国家自然科学基金资助项目(30672339);教育部留学回国人员科研启动基金资助项目(2007)

Establishment of a green fluorescent protein-labeled mouse model of adenoid cystic carcinoma

Chen Zhenggang1, Dong Zuoqing1, Zhang Dong1, Zhou Chengjun2, Sun Shanzhen3, Liu Shaohua1, Wei Fengcai1   

  1. 1. Dept. of Oral and Maxillofacial Surgery, Qilu Hospital, Shandong University; Stomatology Center of Shandong University, Jinan 250012, China; 2. Dept. of Pathology, The Second Hospital of Shandong University, Jinan 250033, China; 3. Dept. of Pathology, School of Stomatology, Shandong University, Jinan 250012, China
  • Received:2011-08-25 Revised:2011-08-25 Online:2011-08-20 Published:2011-08-20
  • Contact: Liu Shaohua,Tel:0531-82169247

摘要:

目的建立能够实时监测、连续动态观察腺样囊性癌生长、转移的裸鼠模型。方法用逆转录病毒载体pLEGFP-N1感染腺样囊性癌细胞系ACCM并筛选出ACCM-GFP稳定细胞株,并比较ACCM和ACCM-GFP细胞的增殖特性和形态特点;用ACCM-GFP细胞种植法建立裸鼠舌癌模型,对移植瘤的生长进行实时荧光成像观察,并与ACCM肿瘤进行组织学比较。结果ACCM-GFP细胞可长期稳定表达GFP;ACCM和ACCM-GFP细胞的增殖特性和形态无差异,体内成瘤的组织学表现无差异;通过活体荧光成像系统可实时监测肿瘤的生长。结论ACCM-GFP裸鼠荧光肿瘤模型可以长期无创、实时、动态观察肿瘤的生长变化,是进行腺样囊性癌基础和临床研究的理想肿瘤模型。

关键词: 腺样囊性癌, 绿色荧光蛋白, 肿瘤模型, 动物模型

Abstract:

Objective To establish a novel nude mice model which can be visualized in real time and detected in a continuous and dynamic way for the development and metastasis of adenoid cystic carcinoma. Methods Human adenoid cystic carcinoma cells, ACCM cell line, were infected with retroviral vector of pLEGFP-N1 and then screened for a single colony of ACCM-GFP cells. Cell proliferation and morphological analysis were conducted for ACCM and ACCMGFP cells. Nude mice lingual carcinoma model was set up with ACCM-GFP cells injection and real time observation with fluorescence imaging on ACCM-GFP tumors was performed subsequently. Histological assay was analyzed for ACCM and ACCM-GFP tumors as well. Results ACCM-GFP cells were able to express GFP stably in the long term. ACCM and ACCM-GFP cells showed no significant difference in cell proliferation and morphology, and no significant difference of histological characteristics in vivo could be found between ACCM and ACCM-GFP tumors. Tumor development could be monitored in real time with fluorescence imaging system in vivo. Conclusion GFP-expressing ACCM tumor model can be applied to detect and observe its development in the long term in a noninvasive, real time and dynamic way. It is also a kind of ideal in vivo mouse model for adenoid cystic carcinoma research.

Key words: adenoid cystic carcinoma, green fluorescent protein, tumor model, animal model