中国寄生虫学与寄生虫病杂志 ›› 2009, Vol. 27 ›› Issue (3): 9-231.

• 实验研究 • 上一篇    下一篇

人包皮成纤维细胞和人子宫颈癌细胞体外培养弓形虫速殖子

吴亮1, 章秋霞1, 李婷婷1, 陈盛霞1 *, 曹建平2   

  1. 1 江苏大学基础医学与医学技术学院, 镇江 212013; 2 中国疾病预防控制中心寄生虫病预防控制所, 卫生部寄生虫病原与媒介生物学重点实验室, 上海 200025
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2009-06-30 发布日期:2009-06-30
  • 通讯作者: 陈盛霞

In vitro Culture of Toxoplasma gondii Tachyzoites in HFF and Hela Cells

WU Liang1, ZHANG Qiu-xia1, LI Ting-ting1, CHEN Sheng-xia1 *, CAO Jian-ping2   

  1. 1 School of Medical Science and Laboratory Medicine, Jiangsu University, Zhenjiang 212013, China;2 National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, Laboratory of Parasite and Vector Biology, MOH, Shanghai 200025, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2009-06-30 Published:2009-06-30
  • Contact: CHEN Sheng-xia

摘要: 目的 比较弓形虫RH株速殖子在人包皮成纤维细胞(human foreskin fibroblast, HFF)和人子宫颈癌(HeLa)细胞的感染和细胞内增殖情况。 方法 分别于含一盖玻片的细胞培养皿(35 mm)内培养HFF细胞和HeLa细胞。待形成单细胞层后各加入经3 μm滤膜纯化的弓形虫RH株速殖子共培养, 分别于0.5、1、2、4、8、12、24、36、48、72和96 h取出盖玻片, 经吉氏染色镜下观察速殖子在两种细胞内的增殖情况。 结果 与HFF细胞共培养4 h后, 速殖子即可侵入HFF细胞, 1个细胞内可见数十个速殖子;24 h可见明显的假包囊, 72 h细胞被胀破。而与HeLa细胞共培养8 h后速殖子才侵入细胞, 每个细胞内可见3~5个速殖子, 48 h形成假包囊, 96 h大部分细胞被胀破。 结论 弓形虫RH株速殖子可在HFF细胞和HeLa细胞内增殖, 在HFF细胞内的增殖速度快于HeLa细胞。

关键词: 刚地弓形虫, 速殖子, 体外培养, HFF细胞, HeLa细胞

Abstract: Objective To study the proliferation of Toxoplasma gondii RH strain tachyzoites in human foreskin fibroblast (HFF) cells and HeLa cells. Methods HFF cells and HeLa cells were cultured in 35 mm cell culture dishes with glass cover slip. Confluent cells were co-cultured with tachyzoites which purified by 3 μm filter membrane. At 0.5, 1 , 2, 4, 8, 12, 24, 36, 48, 72, and 96 h after co-culture, the invasion of tachyzoites into the cells and proliferation in cells were observed with Giemsa staining. Results In 4 h after co-culture, there were dozens of T.gondii tachyzoites in the HFF cells. At 24 h many pseudocysts emerged. At 72 h most of the cells were destroyed by tachyzoites. While cultured in HeLa cells for 8 h, there were only 3-5 tachyzoites in one cell, and pseudocysts emerged at 48 h. At 96 h after co-culture, most cells were destroyed. Conclusion T. gondii tachyzoites can be cultured in HFF cells and HeLa cells. The proliferation of tachyzoites in HFF cells was quicker than that in HeLa cells.

Key words: Toxoplasma gondii, Tachyzoite, In vitro culture, HFF cell, HeLa cell