Wang Li-Wei, Chen Li-Xin, Jacob Tim
Department of Physiology and Laboratory of Cell Biology, Guangdong Medical College, Zhanjiang, Guangdong 524023, China.
Sheng Li Xue Bao. 2004 Apr 25;56(2):230-6.
The immunofluorescence approach, the confocal microscopy and the patch-clamp technique were used to investigate the expression of ClC-3 (one of the candidates of volume-activated chloride channels) and its relationships with the volume-activated chloride current and the capacity of regulatory volume decrease (RVD) in the cell cycle of nasopharyngeal carcinoma cells (CNE-2Z cells). The results indicated that CNE-2Z cells expressed ClC-3. ClC-3 was located predominantly inside the cells but not in the membrane. Both the expression level and the distribution of ClC-3 were cell cycle dependent. ClC-3 expression was low in G1 but high in S phase. The cells in G2/M phase possessed an intermediate level of the expression. ClC-3 expression level was negatively correlated to the RVD capacity and amplitude of the volume-activated chloride current in the cell cycle. The results suggest that ClC-3 may be an important factor in the regulation of cell cycle progression, but that it is probably not the chloride channel associated with RVD in these cancer cells.
采用免疫荧光法、共聚焦显微镜和膜片钳技术,研究容积激活氯通道候选分子之一ClC-3在鼻咽癌细胞(CNE-2Z细胞)细胞周期中的表达及其与容积激活氯电流和调节性容积减小(RVD)能力的关系。结果表明,CNE-2Z细胞表达ClC-3。ClC-3主要位于细胞内而非细胞膜上。ClC-3的表达水平和分布均依赖于细胞周期。ClC-3在G1期表达低,在S期表达高。G2/M期细胞的表达水平处于中间水平。在细胞周期中,ClC-3表达水平与RVD能力和容积激活氯电流幅度呈负相关。结果提示,ClC-3可能是调节细胞周期进程的重要因素,但可能不是这些癌细胞中与RVD相关的氯通道。