Bioelectrorheological model of the cell. 2. Analysis of creep and its experimental verification
Abstract
The electrorheological model of the cell proposed in Part 1 of this work was used to analyze changes in time of the shape of a cell acted on by a constant-amplitude external alternating electric field, with lossiness of the media taken into account. Shear stress in the cell membrane was determined. This model was then subjected to preliminary experimental verification using Neurospora crassa (slime) spheroplasts subjected to an external alternating electric field of constant frequency (3 MHz) and varying magnitude for different periods of time. Reversible viscoelastic cell deformation and fatigue (stiffening) of the material were observed. A satisfactory fit of the experimental data to Burgers' rheological model was found, and the values of the elastic moduli E1 = 9 X 10(2) N/m2, E2 = 2 X 10(2) N/m2 and viscosities eta 1 = 8 X 10(4) Ns/m2; eta 2 = 7 X 10(3) Ns/m2 were evaluated.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In N. crassa, the bioelectrorheological model predicted changes in cell volume and surface caused by AEFs of 3000 kHz.
“Further testing in N. crassa (mold cells) showed that the model was able to predict changes in cell volume and surface caused by AEFs of 3000 kHz [54].”
From Permeabilizing Cell Membranes with Electric Fields (2021) · cites this paper as [54]
The bioelectrorheological model demonstrates the relationship between AEFs, shape deformations, and membrane destabilization, which can contribute to electroporation and other electric field-induced cell phenomena including electrofusion and electro-destruction.
“The bioelectrorheological model of the cell was proposed and has been expanded upon through a series of manuscripts by Pawlowski et al. [40,53,54,55,56,57] (Figure 3B). This model demonstrates the relationship between AEFs, shape deformations, and membrane destabilization, which can contribute to electroporation and other electric field-induced cell phenomena including electrofusion and electro-d”
From Permeabilizing Cell Membranes with Electric Fields (2021) · cites this paper as [54]
The bioelectrorheological model provides a possible explanation for the causes of electroporation by demonstrating the combined effects of heat energy and extensile stress leading to reversible cell membrane destabilization, which can directly result in electroporation.
“Although the electric field strengths studied by Pawlowski and colleagues [40,53,54,55,56,57] were two orders of magnitude greater than that of TTFields, the bioelectrorheological model provides a possible explanation to the causes of electroporation by demonstrating the combined effects of heat energy and extensile stress leading to reversible cell membrane destabilization, which can directly”
From Permeabilizing Cell Membranes with Electric Fields (2021) · cites this paper as [54]
Both DC and AC electroporation are believed to cause a dielectric breakdown of the cell; the oscillating nature of AC electroporation is thought to provoke structural fatigue of the membrane, comparable to the extensile stress proposed in the bioelectrorheological model.
“Both types of electroporation are believed to cause a dielectric breakdown of the cell. However, the oscillating nature of AC electroporation is thought to provoke structural fatigue of the membrane [61], comparable to the extensile stress proposed in the bioelectrorheological model [40,53,54,55,56,57].”
From Permeabilizing Cell Membranes with Electric Fields (2021) · cites this paper as [54]
Cites
Mechanics and Thermodynamics of Biomembranes
Evans, E. A., Skalak, R., & Weinbaum, S. (1980) · Journal of Biomechanical Engineering · doi:10.1115/1.3138234 · Cited by 961 · see citing works
Structure and function of proton translocating ATPase in plasma membranes of plants and fungi
Serrano, R. (1988) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(88)90017-2 · Cited by 463 · see citing works
Viscoelastic properties of erythrocyte membranes in high-frequency electric fields
Engelhardt, H., Gaub, H. E., & Sackmann, E. (1984) · Nature · doi:10.1038/307378a0 · Cited by 142 · see citing works
Bryant, G., & Wolfe, J. (1987) · The Journal of Membrane Biology · doi:10.1007/bf01869239 · Cited by 133 · see citing works
Slime a plasmodioid variant ofNeurospora crassa
Emerson, S. (1964) · Genetica · doi:10.1007/bf01664188 · Cited by 78 · see citing works
Ultrastructure and Invertase Secretion of the Slime Mutant of Neurospora crassa
Bigger, C. H., WHITE, M. R., & Braymer, H. D. (1972) · Journal of General Microbiology · doi:10.1099/00221287-71-1-159 · Cited by 34 · see citing works
Temperature-induced modifications of glycosphingolipids in plasma membranes of Neurospora crassa
Aaronson, L. R., & Martin, C. E. (1983) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(83)90300-0 · Cited by 29 · see citing works
Scarborough, G. A. (1978) · Methods in cell biology · doi:10.1016/s0091-679x(08)62014-2 · Cited by 26 · see citing works
Morphology of slime variants of Neurospora crassa growing on a glass surface in liquid medium
Trevithick, J. R., & Galsworthy, P. R. (1977) · Archives of Microbiology · doi:10.1007/bf00406363 · Cited by 15 · see citing works
Electrofusion ofNeurospora crassaslime cells
Fikus, M., Grzesiuk, E., Marszałek, P., Rózycki, S., & Zieliński, J. (1985) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1985.tb01651.x · Cited by 11 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Permeabilizing Cell Membranes with Electric Fields
Aguilar, A. A., Ho, M. C., Chang, E., Carlson, K. W., Natarajan, A., Marciano, T., Bomzon, Z., & Patel, C. B. (2021) · Cancers · doi:10.3390/cancers13092283 · Cited by 76 · see citing works
Abou-Dakka, M., Herrera-Valencia, E. E., & Rey, A. D. (2012) · Journal of Non-Newtonian Fluid Mechanics · doi:10.1016/j.jnnfm.2012.07.007 · Cited by 27 · see citing works
Pawłowski, P., Szutowicz, I., Marszałek, P., & Fikus, M. (1993) · Biophysical Journal · doi:10.1016/s0006-3495(93)81056-7 · Cited by 25 · see citing works
Self-citationActuation of flexoelectric membranes in viscoelastic fluids with applications to outer hair cells
Herrera-Valencia, E. E., & Rey, A. D. (2014) · Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rsta.2013.0369 · Cited by 24 · see citing works
Bioelectrorheological model of the cell. 3. Viscoelastic shear deformation of the membrane
Poznański, J., Pawłowski, P., & Fikus, M. (1992) · Biophysical Journal · doi:10.1016/s0006-3495(92)81866-0 · Cited by 21 · see citing works
Self-citationPawłowski, P., & Fikus, M. (1993) · Biophysical Journal · doi:10.1016/s0006-3495(93)81055-5 · Cited by 11 · see citing works
Self-citationRamírez-Torres, L. A., Herrera-Valencia, E. E., Sánchez-Villavicencio, M. L., Soriano‐Correa, C., Hernández-Abad, V. J., & Calderas, F. (2024) · Physics of Fluids · doi:10.1063/5.0189731 · Cited by 9 · see citing works
Electrorheological Model Based on Liquid Crystals Membranes with Applications to Outer Hair Cells
Herrera-Valencia, E. E., & Rey, A. D. (2018) · Fluids · doi:10.3390/fluids3020035 · Cited by 9 · see citing works
Bioelectrorheological Model of the Cell. 7. Cellular Deformation in the Presence of Cytochalasin B.
Pawłowski, P. H., Poznanska, A., & Fikus, M. (1997) · Biorheology · doi:10.1016/s0006-355x(97)00024-3 · Cited by 4 · see citing works
Self-citationPawłowski, P. H., & Fikus, M. (1998) · Biorheology · doi:10.1016/s0006-355x(99)80013-4
Self-citationA Brief Sketch of the History of EMB: Where Good Ideas Come From
Brosseau, C. (2023) · Studies in mechanobiology, tissue engineering and biomaterials · doi:10.1007/978-3-031-37981-9_3
- Authors
- Fikus, M., & Pawlowski, P.
- Affiliations
- Institute of Biochemistry and Biophysics, Polish Academy of Sciences (PL)
- Venue
- Journal of Theoretical Biology
- Publisher
- Elsevier BV
- Published
- 1989-04
- Volume
- 137
- Issue
- 4
- Pages
- 365-373
- ISSN
- 0022-5193 (ISSN-L)
- OpenAlex
- W2061373740
- Cited by
- 11
- References
- 10
- Citations by year
- 2024: 1 · 2023: 1 · 2021: 1 · 2018: 1 · 2014: 1 · 2012: 1
- FWCI
- 0.15
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Theoretical Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Electromagnetic Fields and Biological Effects
- Physical Sciences › Chemical Engineering › Fluid Flow and Transfer Processes › Rheology and Fluid Dynamics Studies
- Keywords
- viscoelasticity, AC electric field, Burgers model, elastic modulus, viscosity, cell deformation, lossy media
- MeSH terms
- Cell Membrane, Mathematics, Models, Biological, Neurospora crassa, Rheology, Stress, Mechanical
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review