Establishment of HEK293 cell line expressing green fluorescent protein-aquaporin-1 to determine osmotic water permeability

被引:10
作者
Gao, JW
Yu, HM
Song, QL
Li, XJ [1 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Dept Pharmacol, Beijing 100083, Peoples R China
[2] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China
[3] Natl Res Inst Family Planning, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
osmotic water permeability; fluorescence density; transfected cell; aquaporin-1 (AQP1);
D O I
10.1016/j.ab.2005.03.033
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aquaporin (AQP) is a kind of channel-forming membrane glycoprotein that mediates osmotic water transport. The present study aimed to establish a cell line stably transfected with AQP1 to measure osmotic water permeability. The recombinant plasmid was constructed by subcloning the full-length rat AQP1 cDNA into pEGFP-C3 vector, named pEGFP/AQP1. Human embryonic kidney 293 cells were transfected with pEGFP/AQP1 and selected by G418 to obtain a cell line stably expressing AQP1 tagged with green fluorescent protein. The expression level of AQPI in the stably transfected cell was detected by reverse transcription polymerase chain reaction and Western blot. The real-time change of fluorescence density, corresponding to cell swelling induced by hyposmotic solution, was recorded under confocal laser scanning microscope and used to assess osmotic water permeability. The typical AQP1 inhibitor, mercuric chloride, validated this osmotic water permeability assay. These results suggested that this transfected cell model could be conveniently used to determine osmotic water permeability. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:53 / 58
页数:6
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