期刊文献+

氯通道在不同生长周期的鼻咽癌细胞迁移中的作用 被引量:4

Roles of chloride channels in the migration of nasopharyngeal carcinoma cells at different stages of the cell cycle
在线阅读 下载PDF
导出
摘要 目的:研究不同生长周期的鼻咽癌低分化上皮细胞(CNE-2Z)的迁移能力及氯通道在迁移过程中所起的作用。方法:运用血清饥饿法、化学药物双阻断法、有丝分裂药物阻断及摇落法分别将CNE-2Z细胞同步化至细胞周期的G1、S、M期,流式细胞仪检测其同步化效果。结合应用迁移小室和图像分析法,测定迁移率。台盼蓝活细胞染色法测定药物的细胞毒性。结果:不同生长周期的细胞迁移能力不同,G1期细胞迁移能力最强,随后是M期,S期迁移能力最弱。氯通道阻断剂(ATP、NPPB、tamoxifen)抑制CNE-2Z细胞迁移,但不同的氯通道阻断剂对不同生长周期CNE-2Z细胞迁移的阻滞效应不相同。结论:CNE-2Z细胞的迁移能力与其所在的生长周期密切相关,氯通道在各期CNE-2Z细胞的迁移过程中起着重要作用。 AIM: To clarify the migration capability of nasopharyngeal carcinoma cells (CNE - 2Z) at different stages of the cell cycle and the roles of chloride channels in cell migration. METHODS: Synchronous cells were obtained by the serum deprivation, double chemical - block, mitotic arrest and shake - off techniques. Cell cycle distribution of CNE - 2Z cells was analyzed by the flow cytometry. Migration rate was assayed by transwell chambers and by image analysis. The cytotoxicity of chemicals on cells was tested by MTT assay. RESULTS: CNE - 2Z cells at different stages of the cell cycle exhibited different migratory ability. The migration rate of the three stages was G1 〉 M 〉 S. The migration of CNE - 2Z cells was inhibited by chloride channel blockers (ATP, NPPB and tamoxifen), but the inhibitory effect of the blockers varied with cells at different stages. CONCLUSIONS: The migratory ability is associated with the cell cycle in CNE - 2Z cells. Chloride channels play an important role in cell migration of CNE- 2Z cells.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2005年第9期1783-1786,共4页 Chinese Journal of Pathophysiology
基金 英国TheWellcomeTrust资助(No.056909/299/Z) 中国教育部资助(No.GJ9901) 广东省卫生厅资助项目(No.A2001474)
关键词 鼻咽肿瘤 细胞运动 氯通道 细胞周期 Nasopharyngeal neoplasms Cell movement Chloride channels Cell cycle
  • 相关文献

参考文献3

二级参考文献15

  • 1Chen L,Am J Physiol,1999年,276卷,C182页
  • 2Wu J,J Physiol,1996年,491卷,743页
  • 3Villaz M, Cinniger JC, Moody WJ. A voltage-gated chloride channel in ascidian embryos modulated by both the cell cycle clock and cell volume[J]. J Physiol, 1995,488(3): 689-699.
  • 4Bubien JK, Kirk KL, Rado TA, et al. Cell cycle dependence of chloride permeability in normal and cystic fibrosis lymphocytes[J]. Science,1990, 248(4961): 1416-1419.
  • 5Ullrich N, Sontheimer H. Cell cycle-dependent expression of a glioma-specific chloride current: proposed link to cytoskeletal changes[J]. Am J Physiol ,1997,273(4): C1290-C1297.
  • 6Voets T, Wei L, De Smet P, et al. Downregulation of volume-activated Cl-currents during muscle differentiation[J]. Am J Physiol, 1997,272(2): C667-C674.
  • 7Lang F, Busch GL, Ritter M, et al. Functional significance of cell volume regulatory mechanisms[J]. Physiol Rev, 1998, 78 (1): 247-306.
  • 8Chen L, Wang L, Zhu L, et al. Cell cycle dependent expression of volume-activated chloride currents in nasopharyngeal carcinoma cells (CNE-2Z)[J]. Am J Physiol, 2002,283(4), C1313-C1323.
  • 9Hurnak O, Zachar J. Conductance-voltage relations in large-conductance chloride channels in proliferating L6 myoblasts[J]. Gen Physiol Biophys, 1994,13(3): 171-192.
  • 10Mandlekar S, Kong AN. Mechanisms of tamoxifen-induced apoptosis[J]. Apoptosis, 2001, 6(6): 469-477.

共引文献29

同被引文献18

引证文献4

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部