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迁移的鼻咽癌细胞容积激活性氯电流
引用本文:Mao JW,Wang LW,Sun XR,Zhu LY,Li P,Zhong P,Nie SH,Jacob T,Chen LX. 迁移的鼻咽癌细胞容积激活性氯电流[J]. 生理学报, 2004, 56(4): 525-530
作者姓名:Mao JW  Wang LW  Sun XR  Zhu LY  Li P  Zhong P  Nie SH  Jacob T  Chen LX
作者单位:广东医学院细胞生物学研究室,湛江 524023;广东医学院细胞生物学研究室,湛江 524023;广东医学院生理研究室,湛江 524023;广东医学院生理研究室,湛江 524023;School of Biosciences,cardiff CF10 3US.UK
基金项目:This work was supported by grants from the Wellcome Trust UK (056909/299/Z),the Ministry of Education China (GJ9901),the Health Department of Guangdong Province (A2001474).
摘    要:用膜片钳技术研究了Transwell小室趋化迁移后的鼻咽癌CNE-2Z细胞容积激活性CT电流。47%低渗刺激迁移后的CNE-2Z细胞诱发容积激活性氯电流,与未迁移细胞相比,其特性以及其对氯通道阻断剂的敏感性发生明显的变化,此电流的密度明显高于未迁移细胞,而且该电流几乎完全被氯通道阻断剂adenosine-5'-triphosphate(ATP,10 mmol/L)、5-nitro-2-3-phenylpropylamino benzoic acid(NPPB,100μmol/L)和他莫昔芬(30μmol/L)抑制,其中NPPB和他莫昔芬对迁移细胞的抑制作用明显强于未迁移细胞。迁移后的CNE-2Z细胞容积激活性氯通道对阴离子的通透性为:Br>Cl>I>葡萄糖酸,与未迁移细胞(I>Br>Cl>葡萄糖酸)不同。结果提示,容积激活性氯通道可能参与CNE-2Z细胞的迁移过程。

关 键 词:肿瘤细胞  培养的  氯通道  细胞迁移  膜片钳技术

Volume-activated Cl- current in migrated nasopharyngeal carcinoma cells
Mao Jian-Wen,Wang Li-Wei,Sun Xue-Rong,Zhu Lin-Yan,Li Pan,Zhong Ping,Nie Si-Huai,Jacob Tim,Chen Li-Xin. Volume-activated Cl- current in migrated nasopharyngeal carcinoma cells[J]. Acta Physiologica Sinica, 2004, 56(4): 525-530
Authors:Mao Jian-Wen  Wang Li-Wei  Sun Xue-Rong  Zhu Lin-Yan  Li Pan  Zhong Ping  Nie Si-Huai  Jacob Tim  Chen Li-Xin
Affiliation:Laboratory of Cell Biology, Guangdong Medical College, Zhanjiang, Guangdong 524023, China.
Abstract:The transwell chamber migration assay and the patch-clamp technique were used to investigate the volume-activated Cl current (ICl.vol) in migrated nasopharyngeal carcinoma cells (CNE-2Z). 47% hypotonic solution activated a ICl.vol in the migrated CNE-2Z cells. Compared with the control cells (non-migrated), the properties of this current and the sensitivity to Cl channel blockers were changed. The current density in migrated CNE-2Z cells was higher than that in non-migrated cells. The current was almost completely inhibited by extracellular application of adenosine-5'-triphosphate (ATP, 10 mmol/L), 5-nitro-2-3-phenylpropylamino benzoic acid (NPPB, 100 mmol/L) and tamoxifen (30 mmol/L) in all voltage steps applied. The inhibition of NPPB and tamoxifen on the current was stronger in migrated cells than that in non-migrated cells. The permeability sequence of the four anions was Br>Cl>I>Gluconate. The sequence was different from that of the non-migrated cells (I > Br >C1 >Gluconate). The results suggest that volume-activated chloride channels may be involved in the CNE-2Z cell migration.
Keywords:tumor cells  cultured  chloride channels  cell migration  patch-clamp techniques
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