Potentiometric platform for the quantification of cellular potassium efflux

被引:11
作者
Generelli, Silvia [1 ,2 ,3 ]
Jacquemart, Renaud [4 ]
de Rooij, Nico F. [3 ]
Jolicoeur, Mario
Koudelka-Hep, Milena [3 ]
Guenat, Olivier T. [1 ,2 ]
机构
[1] Ecole Polytech, Dept Engn Phys, Montreal, PQ H3C 3A7, Canada
[2] Ecole Polytech, Inst Biomed Engn, Montreal, PQ H3C 3A7, Canada
[3] Univ Neuchatel, Inst Microtechnol, CH-2000 Neuchatel, Switzerland
[4] Ecole Polytech, Dept Chem Engn, Montreal, PQ H3C 3A7, Canada
关键词
D O I
10.1039/b801042k
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Renewed interest in the measurement of cellular K+ effluxes has been prompted by the observation that potassium plays an active and important role in numerous key cellular events, in particular cell necrosis and apoptosis. Although necrosis and apoptosis follow different pathways, both induce intracellular potassium effluxes. Here, we report the use of potassium-selective microelectrodes located in a microfluidic platform for cell culture to monitor and quantify such effluxes in real time. Using this platform, we observed and measured the early signs of cell lysis induced by a modification of the extracellular osmolarity. Furthermore, we were able to quantify the number of dying cells by evaluating the extracellular potassium concentration. A comparison between the potentiometric measurement with a fluoresecent live-dead assay performed under similar conditions revealed the delay between potassium effluxes and cell necrosis. These results suggest that such platforms may be exploited for applications, such as cytotoxicological screening assays or tumor cell proliferation assays, by using extracellular K+ as cell death marker.
引用
收藏
页码:1210 / 1215
页数:6
相关论文
共 26 条
[21]   Osmolytes and mechanisms involved in regulatory volume decrease under conditions of sudden or gradual osmolarity decrease [J].
Ordaz, B ;
Tuz, K ;
Ochoa, LD ;
Lezama, R ;
Peña-Segura, C ;
Franco, R .
NEUROCHEMICAL RESEARCH, 2004, 29 (01) :65-72
[22]   Analysis of single mammalian cells on-chip [J].
Sims, Christopher E. ;
Allbritton, Nancy L. .
LAB ON A CHIP, 2007, 7 (04) :423-440
[23]   Apoptosis recruits two-pore domain potassium channels used for homeostatic volume regulation [J].
Trimarchi, JR ;
Liu, L ;
Smith, PJS ;
Keefe, DL .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 282 (03) :C588-C594
[24]   Roles of K+ channels in regulating tumour cell proliferation and apoptosis [J].
Wang, ZG .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2004, 448 (03) :274-286
[25]   Increased K+ efflux and apoptosis induced by the potassium channel modulatory protein KChAP/PIAS3β in prostate cancer cells [J].
Wible, BA ;
Wang, LM ;
Kuryshev, YA ;
Basu, A ;
Haldar, S ;
Brown, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (20) :17852-17862
[26]   Ion homeostasis and apoptosis [J].
Yu, SP ;
Canzoniero, LMT ;
Choi, DW .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (04) :405-411