Human proximal tubule epithelial cells cultured on hollow fibers: living membranes that actively transport organic cations

被引:84
|
作者
Jansen, J. [1 ,2 ,3 ]
De Napoli, E. [4 ]
Fedecostante, M. [1 ,2 ,3 ]
Schophuizen, C. M. S. [1 ,2 ,3 ]
Chevtchik, N. V. [4 ]
Wilmer, M. J. [1 ]
Van Asbeck, A. H. [5 ]
Croes, H. J. [6 ]
Pertijs, J. C. [1 ]
Wetzels, J. F. M. [7 ]
Hilbrands, L. B. [7 ]
van den Heuvel, L. P. [3 ,8 ]
Hoenderop, J. G. [2 ]
Stamatialis, D. [4 ]
Masereeuw, R. [1 ,9 ]
机构
[1] Radboud Inst Mol Life Sci, Dept Pharmacol & Toxicol, Nijmegen, Netherlands
[2] Radboud Inst Mol Life Sci, Dept Physiol, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Pediat, NL-6525 ED Nijmegen, Netherlands
[4] Univ Twente, MIRA Inst Biomed Technol & Tech Med, Dept Biomat Sci & Technol, NL-7500 AE Enschede, Netherlands
[5] Radboud Inst Mol Life Sci, Dept Biochem, Nijmegen, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Cell Biol, NL-6525 ED Nijmegen, Netherlands
[7] Radboud Univ Nijmegen, Med Ctr, Dept Nephrol, NL-6525 ED Nijmegen, Netherlands
[8] Katholieke Univ Leuven, Dept Pediat Nephrol & Growth & Regenerat, Leuven, Belgium
[9] Univ Utrecht, Dept Pharmaceut Sci, Div Pharmacol, NL-3508 TC Utrecht, Netherlands
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
基金
欧盟第七框架计划;
关键词
CHRONIC KIDNEY-DISEASE; HUMAN RENAL-CELLS; P-CRESYL SULFATE; BIOARTIFICIAL KIDNEY; IN-VITRO; DRUG TRANSPORT; UREMIC ANIMALS; EXPRESSION; PERFORMANCE; REMOVAL;
D O I
10.1038/srep16702
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The bioartificial kidney (BAK) aims at improving dialysis by developing 'living membranes' for cells-aided removal of uremic metabolites. Here, unique human conditionally immortalized proximal tubule epithelial cell (ciPTEC) monolayers were cultured on biofunctionalized MicroPES (polyethersulfone) hollow fiber membranes (HFM) and functionally tested using microfluidics. Tight monolayer formation was demonstrated by abundant zonula occludens-1 (ZO-1) protein expression along the tight junctions of matured ciPTEC on HFM. A clear barrier function of the monolayer was confirmed by limited diffusion of FITC-inulin. The activity of the organic cation transporter 2 (OCT2) in ciPTEC was evaluated in real-time using a perfusion system by confocal microscopy using 4-(4-(dimethylamino) styryl)-N-methylpyridinium iodide (ASP(+)) as a fluorescent substrate. Initial ASP+ uptake was inhibited by a cationic uremic metabolites mixture and by the histamine H2-receptor antagonist, cimetidine. In conclusion, a 'living membrane' of renal epithelial cells on MicroPES HFM with demonstrated active organic cation transport was successfully established as a first step in BAK engineering.
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页数:12
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