Effect of electric field induced transmembrane potential on spheroidal cells: theory and experiment
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Abstract
The transmembrane potential on a cell exposed to an electric field is a critical parameter for successful cell permeabilization. In this study, the effect of cell shape and orientation on the induced transmembrane potential was analyzed. The transmembrane potential was calculated on prolate and oblate spheroidal cells for various orientations with respect to the electric field direction, both numerically and analytically. Changing the orientation of the cells decreases the induced transmembrane potential from its maximum value when the longest axis of the cell is parallel to the electric field, to its minimum value when the longest axis of the cell is perpendicular to the electric field. The dependency on orientation is more pronounced for elongated cells while it is negligible for spherical cells. The part of the cell membrane where a threshold transmembrane potential is exceeded represents the area of electropermeabilization, i.e. the membrane area through which the transport of molecules is established. Therefore the surface exposed to the transmembrane potential above the threshold value was calculated. The biological relevance of these theoretical results was confirmed with experimental results of the electropermeabilization of plated Chinese hamster ovary cells, which are elongated. Theoretical and experimental results show that permeabilization is not only a function of electric field intensity and cell size but also of cell shape and orientation.
Keywords
Chinese hamster ovary cells Electroporation Finite-element modelling Spheroidal cells Transmembrane potentialAbbreviations
Geometry
- a
length of box side
- d
membrane thickness
- gϕϕ and gττ
elements of metric tensor in spheroidal coordinates
- p(ϑ)
arc length on an ellipse
- ri
vector of the point T(x,y,z) lying at the surface of the spheroid
- R
cell radius in the case of a sphere
- R1, R2=R3
axes of cell in the case of a spheroid (prolate spheroid: R 1>R 2=R 3; oblate spheroid R 1<R 2=R 3)
- S
area (surface)
- T
point at the surface of the spheroid
- ρ
ratio between R 1 and R 2
- ϑ, ϕ, r
spherical coordinates
- τ, ϕ, σ
spheroidal coordinates
Electric
- E
applied electric field
- jn
normal component of electric current at the surface of the spheroid
- Li
depolarizing factor in the i=x, y and z directions
- α
azimuth angle in the spherical coordinate system; the angle between the symmetry axis of the spheroid and the external electric field
- β
polar angle in the spherical coordinate system
- φ
electric potential
- σi
conductivity of cytoplasm
- σo
external medium conductivity
- σm
conductivity of cell membrane
- Δφ
transmembrane potential
- Δφc
threshold or critical transmembrane potential
- Δφi
induced transmembrane potential
- Δφr
resting transmembrane potential
Notes
Acknowledgements
The authors thank C. Millot for providing CHO cells. M.G. was supported by a grant from the Association Française contre les Myopathies (AFM). This work was partly supported by the Ministry of Education, Science and Sport of the Republic of Slovenia through various grants and partly by the Cliniporator project (grant QLK3-1999-00484) under the framework of the 5th PRCD of the European Commission.
References
- Bernhardt J, Pauly H (1973) On the generation of potential differences across the membranes of ellipsoidal cells in an alternating electrical field. Biophysik 10:89–98PubMedGoogle Scholar
- Bier M, Hammer SM, Canaday DJ, Lee RC (1999) Kinetics of sealing for transient electropores in isolated mammalian skeletal muscle cells. Bioelectromagnetics 20:194–201CrossRefPubMedGoogle Scholar
- Brock TD, Smith DW, Madigan MT (1984) Biology of microorganisms. Prentice-Hall, Engelwood Cliffs, NJ, USAGoogle Scholar
- Eynard N, Rodriguez F, Trotard J, Teissié J (1998) Electrooptics studies of Escherichia coli electropulsation: orientation, permeabilization, and gene transfer. Biophys J 75:2587–2596PubMedGoogle Scholar
- Fear CE, Stuchly MA (1998) Modeling assemblies of biological cells exposed to electric eields. IEEE Trans Biomed Eng 45:1259–1271CrossRefPubMedGoogle Scholar
- Fricke H (1925) A mathematical treatment of the electrical conductivity and capacity of disperse systems. II. The capacity of conducting spheroids surrounded by a non-conducting membrane for a current of low frequency. Phys Rev 26:678CrossRefGoogle Scholar
- Gabriel B, Teissié J (1998) Fluorescence imaging in the millisecond time range of membrane electropermeabilisation of single cells using a rapid ultra-low-light intensifying detection system. Eur Biophys J 27:291–298CrossRefGoogle Scholar
- Gimsa J, Wachner D (2001) Analytical description of the transmembrane voltage induced on arbitrarily oriented ellipsoidal and cylindrical cells. Biophys J 81:1888–1896PubMedGoogle Scholar
- Hart FX, Marino AA (1982) ELF dosage in ellipsoidal model of men due to high voltage transmission lines. J Bioelec 1:129–154Google Scholar
- Korn GA, Korn TM (2000) Mathematical handbook for scientists and engineers. Dover, Mineola, NY, USAGoogle Scholar
- Kotnik T, Miklavčič D (2000) Analytical description of transmembrane voltage induced by electric fields on spheroidal cells. Biophys J 79:670–679PubMedGoogle Scholar
- Kotnik T, Bobanović F, Miklavčič D (1997) Sensitivity of transmembrane voltage induced by applied electric fields: a theoretical analysis. Bioelectrochem Bioenerg 43:285–291CrossRefGoogle Scholar
- Krasznai Z, Marian T, Balkay L, Emri M, Tron L (1994) Flow cytometric determination of absolute membrane potential of cells. J Photochem Photobiol 28:93–99CrossRefGoogle Scholar
- Miklavčič D, Šemrov D, Mekid H, Mir LM (2000) A validated model of in vivo electric field distribution in tissues for electrochemotherapy and for DNA electrotransfer for gene therapy. Biochim Biophys Acta 1523:73–83PubMedGoogle Scholar
- Miller CE, Henriqez CS (1988) Three-dimensional finite element solution for biopotentials: erythrocyte in an applied field. IEEE Trans Biomed Eng 35:712–718CrossRefPubMedGoogle Scholar
- Mir LM (2001) Therapeutic perspectives of in vivo cell electropermeabilization. Bioelectrochemistry 53:1–10CrossRefPubMedGoogle Scholar
- Neumann E (1989) The relaxation hysteresis of membrane electroporation. In: Neumann E, Sowers AE, Jordan CA (eds) Electroporation and electrofusion in cell biology. Plenum, New York, pp 61–82Google Scholar
- Neumann E, Schaefer-Ridder M, Wang Y, Hofschneider PH (1982) Gene transfer into mouse lyoma cells by electroporation in high electric fields. EMBO J 1:841–845PubMedGoogle Scholar
- Pavlin M, Pavšelj N, Miklavčič D (2002) Dependence of induced transmembrane potential on cell density, arrangement, and cell position inside the cell system. IEEE Trans Biomed Eng 49:605–612CrossRefPubMedGoogle Scholar
- Rols MP, Teissié J (1998) Electropermeabilization of mammalian cells to macromolecules: control by pulse duration. Biophys J 75:1415–1423PubMedGoogle Scholar
- Rols MP, Delteil C, Golzio M, Dumond P, Cros S, Teissie J (1998a) In vivo electrically mediated protein and gene transfer in murine melanoma. Nat Biotechnol 16:168–171PubMedGoogle Scholar
- Rols MP, Delteil C, Golzio M, Teissié J (1998b) In vitro and ex vivo electrically mediated permeabilization and gene transfer in murine melanoma. Bioelectrochem Bioenerg 47:129–134CrossRefGoogle Scholar
- Satkauskas S, Bureau MF, Puc M, Mahfoudi A, Scherman D, Miklavcic D, Mir LM (2002) Mechanisms of in vivo DNA electrotransfer: respective contributions of cell electropermeabilization and DNA electrophoresis. Mol Ther 5:133–140CrossRefPubMedGoogle Scholar
- Schwan HP (1957) Electrical properties of tissue and cell suspensions. Adv Biol Med Phys 5:147–209Google Scholar
- Schwarz G, Saito M, Schwan HP (1965) On the orientation of nonspherical particles in an alternating electrical field. J Chem Phys 10:3562–3569Google Scholar
- Šemrov D, Miklavčič D (1998) Calculation of the electrical parameters in electrochemotherapy of solid tumours in mice. Comput Biol Med 28:439–448CrossRefPubMedGoogle Scholar
- Serša G, Čemažar M, Šemrov D, Miklavčič D (1996) Changing electrode orientation improves the efficacy of electrochemotherapy of solid tumors in mice. Bioelectrochem Bioenerg 39:61–66CrossRefGoogle Scholar
- Sillars RW (1937) The properties of dielectrics containing semiconducting particles various shapes. J Inst Elec Eng 80:378–394Google Scholar
- Stratton JA (1941) Electromagnetic theory. McGraw-Hill, New YorkGoogle Scholar
- Sukharev SI, Klenchin VA, Serov SM, Chernomordik LV, Chizmadzhev YA (1992) Electroporation and electrophoretic DNA transfer into cells. The effect of DNA interaction with electropores. Biophys J 63:1320–1327PubMedGoogle Scholar
- Susil R, Šemrov D, Miklavčič D (1998) Electric field-induced transmembrane potential depends on cell density and organization. Elec Magnetobiol 17:391–399Google Scholar
- Teissié J, Blangero C (1984) Direct experimental evidence of the vectorial character of the interaction between electric pulses and cells in cell electrofusion. Biochim Biophys Acta 775:446–448PubMedGoogle Scholar
- Teissié J, Rols MP (1993) An experimental evaluation of the critical potential difference inducing cell membrane electropermeabilization. Biophys J 65:409–413PubMedGoogle Scholar
- Tekle E, Astumian RD, Chock PB (1990) Electro-permeabilization of cell membranes: effect of the resting membrane potential. Biochem Biophys Res Commun 172:282–287PubMedGoogle Scholar
- Weaver JC, Chizmadzhev YA (1996) Electroporation. In: Polk C, Postow E (eds) Biological effects of electromagnetic fields. CRC, Boca Raton, Fla., USA, pp 247–274Google Scholar
- Weaver JC, Powell KT (1989) Theory of electroporation. In: Neumann E, Sowers AE, Jordan CA (eds) Electroporation and electrofusion in cell biology. Plenum, New York, pp 111–112Google Scholar
- Zimmermann U (1982) Electric field-mediated fusion and related electrical phenomena. Biochim Biophys Acta 694:227–277CrossRefPubMedGoogle Scholar
- Zimmermann U, Pilwat G, Riemann F (1974) Dielectric breakdown of cell membranes. Biophys J 14:881–899PubMedGoogle Scholar