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Electrotaxis

(Redirected from Galvanotaxis)

Electrotaxis, also known as galvanotaxis, is the directed motion of biological cells or organisms guided by an electric field or current.[1] The directed motion of electrotaxis can take many forms, such as; growth, development, active swimming, and passive migration.[1][2] A wide variety of biological cells can naturally sense and follow DC electric fields. Such electric fields arise naturally in biological tissues during development and healing.[3][4] These and other observations have led to research into how applied electric fields can impact wound healing[5][6][7] An increase in wound healing rate is regularly observed and this is thought to be due to the cell migration and other signaling pathways that are activated by the electric field.[8] Additional research has been conducted into how applied electric fields impact cancer metastasis, morphogenesis, neuron guidance, motility of pathogenic bacteria, biofilm formation, and many other biological phenomena.[2][9][10][11]

History

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In 1889, German physiologist Max Verworn applied a low-level direct current to a mixture of bacterial species and observed that some moved toward the anode and others moved to the cathode.[12] Two years later, in 1891, Belgian microscopist E. Dineur made the first known report of vertebrate cells migrating directionally in a direct current, a phenomenon which he coined galvanotaxis.[13] Dineur used a zinc–copper cell to apply a constant current to the abdominal cavity of a frog via a pair of platinum electrodes. He found that inflammatory leukocytes aggregated at the negative electrode. Since these pioneering studies, a variety of different cell types and organisms have been shown to respond to electric fields.[10]

Mechanism

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Understanding of the underlying mechanisms that cause electrotaxis to occur is limited. The diversity of biological cells and environmental conditions make it likely that there are many different mechanisms that allow for cells to migrate due to electric fields. Some studies have indicated that certain organisms move passively without any specific sensing mechanisms applied to alter active motility.[14][15]

Bacteria

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In a sufficiently strong electric field, small cells may move as uniformly charged particles[16] or dipoles.[17] Other research reports suggest that bacteria cells might perceive local electric fields via chemotaxis.[18][19][20] This is done by sensing redox molecules that have formed a gradient relative to the poised electrical surface in the local environment.

Mammalian cells

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The method of detection of a field in mammalian cells is under active investigation and might involve several mechanisms. For now, it is thought that redistribution of membrane-bound sensors dragged by Coulombic forces and electro-osmosis at the membrane would cause the cell to polarize, then migrate.[21] Mathematical modeling suggests that a 6-10% change in sensor concentration across the cell is detectable.[22] Experiments that repeatedly changed orientation of a field applied to several cell lines suggest that sensor polarization occurs on a relatively rapid timescale, perhaps several seconds, compared to the cell migration response, which is observed after 5-10 minutes.[23] This allows cells to time-average changes in the direction of the electric field before migrating.[23]

Evidence for a mechanism

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There has been no discovery of a single mechanism or process by which all cells undergo electrotaxis.[24] However, multiple explanations have been investigated, resulting in a considerable body of evidence and a limited understanding of how cells migrate using electric fields. Electrotaxis is thought to operate based on changes in Ca2+ concentration produced by direct-current electric fields (dcEFs) due to the fact that exposure to dcEFs can cause concentration changes in excess of 1 millimolar. Additionally, calcium channel inhibition using Co2+ or D600 was observed to prevent electotaxis in most cases.[25] Cells that exhibit electrotaxis undergo an influx of Ca2+ ions on the anodal side of the cell, and simultaneous decrease in concentration on that cathodal side. This rearrangement is thought to create "push-pull" forces that induce net movement in the cathodal direction. However, this process would be more complicated in cells with intercellular calcium stores or voltage-gated calcium channels. In addition, voltage-gated sodium channels, protein kinases, growth factors, surface charge, and protein electrophoresis have been observed to have a role in electrotaxis.[25] However, there is no knowledge of a sensor molecule used specifically for electrotaxis.[26] The exact role and function of these and other cellular components in electrotaxis is not fully understood and is the basis of ongoing research.[25]

Signaling pathways used in electrotaxis

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In the absence of a complete explanation of the mechanism behind electrotaxis, certain signaling pathways have been found to have an involvement in electrotaxis. In both neutrophils and keratinocytes, Zhau et. al. experimentally determined that physiological strength EFs induce phosphorlyation of extracellular-signal-regulated kinase (ERK), p38 mitogen-activated Kinase (MAPK), Src, and Akt on ser 473. In chemotaxis, Src and Akt are polarized by phosphatidylinositol-3-OH kinase-γ (PI(3)Kγ) activation and inhibition of phosphate tensin homolog (PTEN).[27] In the experiment, phosphorylated Src polarized in the direction of migration when influnenced by physiological strength EFs, as is also seen in chemotaxis. Phosphatidylinositol-3,4,5-triphosphate (PtdIns(3,4,5)P3), another molecule used in signaling, polarized to the leading edge of HL60 cells when subjected to an EF. Upon reversal of the EF, polarization PtdIns(3,4,5)P3 rapidly reversed to the new direction of migration. Treatment with lantruculin did not prevent this from occurring, indicating that polarization is not actin-dependent. Cells in which the gene encoding PI(3)Kγ, Pik3cg, was disrupted exhibited reduced electrotaxic responses. Pharmocological inhibition of PI(3)K in keratinocytes produced the same results. Similarly, genetic disruption of PTEN resulted in increased phosphorylation of ERK and Akt and a greater electrotaxic response.[27] Consideration of these results suggests that PI(3)Kγ and PTEN are involved in the signaling pathway used in electrotaxis.

Role in wound healing

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A transepithelial potential (TEP) is created by a difference in ion concentrations across a tissue barrier in the body. In humans, a gradient exists between the outermost and innermost layers of skin across the entire body. This gradient can range from 10mV to 60mV, depending on which part of the body is measured. The potential is created by epithelial cells, which pump Cl- ions out of the skin through the apical membrane and transport Na+ ions to the basal side of the epithelium.[26] This is supported by an experiment in which Na+ and Cl- transport was increased by addition of AgNO3, and a corresponding increase in membrane potential was observed. Furosemide, a Cl- efflux inhibitor, also decreased the strength of the field in corneal cells.[27] These potentials are maintained elsewhere on the body, such as in the GI, urinary, and respiratory ducts, as well as the corneal epithelium.[26][28] When the epithelium is pierced by some kind of wound, the barrier which establishes the electric potential has been removed, and so the TEP cannot be maintained. This creates a lateral EF, running from intact epithelium toward the edges of the wound.[26][29] These wound EFs last as long as the wound takes to heal, and are involved in guiding various types of cells toward the injury in order to facilitate recovery[26][30] These lateral fields arise instantaneously upon disruption of the epithelium and gradually increase to their maximum strength. The current strength then declines but is maintained throughout the healing process. The strength and direction of these fields are the same regardless of the size of a wound.[27]

Healing of skin wounds is a complex process involving the cooperation of various elements of the body, such as platelets, immune cells, epithelial cells, and fibroblasts. This process is coordinated largely by chemical signals, but there is evidence that electrotaxis plays an additional role in directing specific cell types toward the site of an injury.[26] During the proliferation phase of recovery, keratinocytes move toward the cathodal side of the EFs occurring around and injury, bringing them toward the edge of the wound. In fact, in vitro experimentation found that application of physiological strength EFs could override other signals and guide cells to migrate towards or even away from a wound depending on the direction of the field, regardless of chemical factors.[27] EFs have also experimentally been found to influence cell migration in human umbilical vein cells, dermal fibroblasts, and myofibroblasts.[26]

Role in cancer metastasis

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Cancer metastasis is the process by which a tumor spreads from its place of origin in the body to distant tissues. Cancer cells and tumors have been known to produce and respond to electrical currents within the body. Cancer cells isolated from brain, prostate, and lung tumors have all been observed to have electrotaxis responses, and it there is evidence suggesting that electrotaxis may play a role in cancer cell metastasis.[31]

References

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  1. ^ a b Cortese, Barbara; Palamà, Ilaria Elena; D'Amone, Stefania; Gigli, Giuseppe (2014). "Influence of electrotaxis on cell behaviour". Integrative Biology. 6 (9): 817–830. doi:10.1039/c4ib00142g. PMID 25058796.
  2. ^ a b Chong, Poehere; Erable, Benjamin; Bergel, Alain (December 2021). "How bacteria use electric fields to reach surfaces". Biofilm. 3: 100048. doi:10.1016/j.bioflm.2021.100048. PMC 8090995. PMID 33997766.
  3. ^ Jaffe, Lionel F.; Vanable, Joseph W. (July 1984). "Electric fields and wound healing". Clinics in Dermatology. 2 (3): 34–44. doi:10.1016/0738-081X(84)90025-7. PMID 6336255.
  4. ^ Nuccitelli, Richard (2003). A Role for Endogenous Electric Fields in Wound Healing. Current Topics in Developmental Biology. Vol. 58. pp. 1–26. doi:10.1016/S0070-2153(03)58001-2. ISBN 978-0-12-153158-4. PMID 14711011.
  5. ^ Carley, PJ; Wainapel, SF (July 1985). "Electrotherapy for acceleration of wound healing: low intensity direct current". Archives of Physical Medicine and Rehabilitation. 66 (7): 443–6. PMID 3893385.
  6. ^ Gault, Walter R.; Gatens, Paul F. (1 March 1976). "Use of Low Intensity Direct Current in Management of Ischemic Skin Ulcers". Physical Therapy. 56 (3): 265–269. doi:10.1093/ptj/56.3.265. PMID 1083031.
  7. ^ Sven Olof Wikström, Paul Svedman, h; Svedman, P.; Svensson, H.; Tanweer, A. S. (January 1999). "Effect of Transcutaneous Nerve Stimulation on Microcirculation in Intact Skin and Blister Wounds in Healthy Volunteers". Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery. 33 (2): 195–201. doi:10.1080/02844319950159451. PMID 10450577.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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  17. ^ Shi, W; Stocker, B A; Adler, J (February 1996). "Effect of the surface composition of motile Escherichia coli and motile Salmonella species on the direction of galvanotaxis". Journal of Bacteriology. 178 (4): 1113–1119. doi:10.1128/jb.178.4.1113-1119.1996. PMC 177773. PMID 8576046.
  18. ^ Oram, Joseph; Jeuken, Lars J.C. (October 2017). "Shewanella oneidensis MR-1 electron acceptor taxis and the perception of electrodes poised at oxidative potentials" (PDF). Current Opinion in Electrochemistry. 5 (1): 99–105. doi:10.1016/j.coelec.2017.07.013.
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  20. ^ Kim, Beum Jun; Chu, Injun; Jusuf, Sebastian; Kuo, Tiffany; TerAvest, Michaela A.; Angenent, Largus T.; Wu, Mingming (20 September 2016). "Oxygen Tension and Riboflavin Gradients Cooperatively Regulate the Migration of Shewanella oneidensis MR-1 Revealed by a Hydrogel-Based Microfluidic Device". Frontiers in Microbiology. 7: 1438. doi:10.3389/fmicb.2016.01438. PMC 5028412. PMID 27703448.
  21. ^ Allen, Greg M.; Mogilner, Alex; Theriot, Julie A. (April 2013). "Electrophoresis of Cellular Membrane Components Creates the Directional Cue Guiding Keratocyte Galvanotaxis". Current Biology. 23 (7): 560–568. Bibcode:2013CBio...23..560A. doi:10.1016/j.cub.2013.02.047. PMC 3718648. PMID 23541731.
  22. ^ Nwogbaga, Ifunanya; Kim, A Hyun; Camley, Brian A. (2023). "Physical limits on galvanotaxis". Physical Review E. 108 (6–1): 064411. arXiv:2209.04742v2. Bibcode:2023PhRvE.108f4411N. doi:10.1103/PhysRevE.108.064411. PMID 38243498.
  23. ^ a b Zajdel, Tom J.; Shim, Gawoon; Wang, Linus; Rossello-Martinez, Alejandro; Cohen, Daniel J. (June 2020). "SCHEEPDOG: Programming Electric Cues to Dynamically Herd Large-Scale Cell Migration". Cell Systems. 10 (6): 506–514. doi:10.1016/j.cels.2020.05.009. PMC 7779114. PMID 32684277.
  24. ^ Lyon, Johnathan G.; Carroll, Sheridan L.; Mokarram, Nassir; Bellamkonda, Ravi V. (29 March 2019). "Electrotaxis of Glioblastoma and Medulloblastoma Spheroidal Aggregates". Scientific Reports. 9 (1): 5309. Bibcode:2019NatSR...9.5309L. doi:10.1038/s41598-019-41505-6. PMC 6441013. PMID 30926929.
  25. ^ a b c Mycielska, Maria E.; Djamgoz, Mustafa B. A. (1 April 2004). "Cellular mechanisms of direct-current electric field effects: galvanotaxis and metastatic disease". Journal of Cell Science. 117 (9): 1631–1639. doi:10.1242/jcs.01125. PMID 15075225. S2CID 25767554.
  26. ^ a b c d e f g Jia, Naixin; Yang, Jinrui; Liu, Jie; Zhang, Jiaping (June 2021). "Electric Field: A Key Signal in Wound Healing". Chinese Journal of Plastic and Reconstructive Surgery. 3 (2): 95–102. doi:10.1016/S2096-6911(21)00090-X. S2CID 240033107.
  27. ^ a b c d e Zhao, Min; Song, Bing; Pu, Jin; Wada, Teiji; Reid, Brian; Tai, Guangping; Wang, Fei; Guo, Aihua; Walczysko, Petr; Gu, Yu; Sasaki, Takehiko; Suzuki, Akira; Forrester, John V.; Bourne, Henry R.; Devreotes, Peter N.; McCaig, Colin D.; Penninger, Josef M. (July 2006). "Electrical signals control wound healing through phosphatidylinositol-3-OH kinase-γ and PTEN". Nature. 442 (7101): 457–460. Bibcode:2006Natur.442..457Z. doi:10.1038/nature04925. PMID 16871217. S2CID 4391475.
  28. ^ Zhao, Min (August 2009). "Electrical fields in wound healing—An overriding signal that directs cell migration". Seminars in Cell & Developmental Biology. 20 (6): 674–682. doi:10.1016/j.semcdb.2008.12.009. PMID 19146969.
  29. ^ Ji, Ran; Teng, Miao; Zhang, Ze; Wang, Wenping; Zhang, Qiong; Lv, Yanling; Zhang, Jiaping; Jiang, Xupin (2020). "Electric field down-regulates CD9 to promote keratinocytes migration through AMPK pathway". International Journal of Medical Sciences. 17 (7): 865–873. doi:10.7150/ijms.42840. PMC 7163358. PMID 32308539.
  30. ^ Nuccitelli, Richard; Nuccitelli, Pamela; Li, Changyi; Narsing, Suman; Pariser, David M.; Lui, Kaying (September 2011). "The electric field near human skin wounds declines with age and provides a noninvasive indicator of wound healing: Using electric fields to monitor wound healing". Wound Repair and Regeneration. 19 (5): 645–655. doi:10.1111/j.1524-475X.2011.00723.x. PMC 3228273. PMID 22092802.
  31. ^ Zhu, Kan; Hum, Nicholas R.; Reid, Brian; Sun, Qin; Loots, Gabriela G.; Zhao, Min (26 May 2020). "Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis". Scientific Reports. 10 (1): 8712. Bibcode:2020NatSR..10.8712Z. doi:10.1038/s41598-020-65566-0. PMC 7250931. PMID 32457381.
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