Real-time measurement of PMA-induced cellular alterations by microelectrode array-based impedance spectroscopy

被引:14
作者
Rothermel, Andree [1 ]
Nieber, Matthias [1 ]
Mueller, Jana [1 ]
Wolf, Peter [1 ]
Schmidt, Maik [1 ]
Robitzki, Andrea A. [1 ]
机构
[1] Univ Leipzig, Ctr Biotechnol & Biomed, Div Mol Biol Biochem Proc Technol, Fac Biosci Pharm & Psychol, D-04103 Leipzig, Germany
关键词
D O I
10.2144/000112254
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
For a feasible and cost-effective impedance measurement of cellular alterations in real-time, we combined commercially available microelectrode arrays (MEAs), consisting of 60 microelectrodes, with a conventional impedance analyzer. For proof of principle, a breast carcinoma cell line (MCF-7) was cultured on MEAs, and cellular alterations were measured by impedance spectroscopy at a frequency, ranging from 10 Hz to 1 MHz. Cells were stimulated with phorbol 12-myristate 13-acetate (PMA) at different concentrations to activate protein kinase C (PKC)-mediated extra-and intracellular changes. By addition of 0.03 mu M PMA, an increase of the relative impedance (Z(rel)) was observed after 10 min with a maximum at 1 kHz. Moreover a gradual elevation of the impedance was measured 60 min after stimulation with PMA. If 0.3 mu M PMA was applied, the maximal amplitude of the relative impedance after 60 min shifted from 1 kHz (0.03 mu M PMA) to 150 Hz. Subsequently, the impedance was further increased up to 90 min after PMA application, after which the impedance reduced after 240 min. Since we could use MEAs for at least 10 times without affecting the sensitivity, our stud revealed that commercially available MEAs comprising nanocolumnar titanium nitrite electrodes are suitable in microstructures for a highly reproducible and cost-effective multisite measurement of intracellular processes by impedance spectroscopy.
引用
收藏
页码:445 / 450
页数:6
相关论文
共 21 条
[1]   Phorbol ester induced short- and long-term permeabilization of the blood-CSF barrier in vitro [J].
Angelow, S ;
Zeni, P ;
Höhn, B ;
Galla, HJ .
BRAIN RESEARCH, 2005, 1063 (02) :168-179
[2]   Bioelectrical impedance assay to monitor changes in cell shape during apoptosis [J].
Arndt, S ;
Seebach, J ;
Psathaki, K ;
Galla, HJ ;
Wegener, J .
BIOSENSORS & BIOELECTRONICS, 2004, 19 (06) :583-594
[3]   Cellular dielectric spectroscopy: A powerful new approach to label-free cellular analysis [J].
Ciambrone, GJ ;
Liu, VF ;
Lin, DC ;
McGuinness, RP ;
Leung, GK ;
Pitchford, S .
JOURNAL OF BIOMOLECULAR SCREENING, 2004, 9 (06) :467-480
[4]  
Clarke H, 2000, J CELL SCI, V113, P3187
[5]   Potentiation of genomic actions of estrogen by membrane actions in MCF-7 cells and the involvement of protein kinase C activation [J].
Devidze, N ;
Pfaff, DW ;
Kow, LM .
ENDOCRINE, 2005, 27 (03) :253-258
[6]   Protein kinase C (PKC)-δ/-ε mediate the PKC/Akt-dependent phosphorylation of extracellular signal-regulated kinases 1 and 2 in MCF-7 cells stimulated by bradykinin [J].
Greco, S ;
Storelli, C ;
Marsigliante, S .
JOURNAL OF ENDOCRINOLOGY, 2006, 188 (01) :79-89
[7]   NEW FIXED-ARRAY MULTI-MICROELECTRODE SYSTEM DESIGNED FOR LONG-TERM MONITORING OF EXTRACELLULAR SINGLE UNIT NEURONAL-ACTIVITY INVITRO [J].
GROSS, GW ;
RIESKE, E ;
KREUTZBERG, GW ;
MEYER, A .
NEUROSCIENCE LETTERS, 1977, 6 (2-3) :101-105
[8]   Microsystems for isolation and electrophysiological analysis of breast cancer cells from blood [J].
Han, KH ;
Han, A ;
Frazier, AB .
BIOSENSORS & BIOELECTRONICS, 2006, 21 (10) :1907-1914
[9]   Real-time impedance assay to follow the invasive activities of metastatic cells in culture [J].
Keese, CR ;
Bhawe, K ;
Wegener, J ;
Giaever, I .
BIOTECHNIQUES, 2002, 33 (04) :842-+
[10]   Phorbol ester induced changes in tight and adherens junctions in the choroid plexus epithelium and in the ependyma [J].
Lippoldt, A ;
Jansson, A ;
Kniesel, U ;
Andbjer, B ;
Andersson, A ;
Wolburg, H ;
Fuxe, K ;
Haller, H .
BRAIN RESEARCH, 2000, 854 (1-2) :197-206