Endogenous bioelectrical networks store non‐genetic patterning information during development and regeneration

Pattern formation, as occurs during embryogenesis or regeneration, is the crucial link between genotype and the functions upon which selection operates. Even cancer and aging can be seen as challenges to the continuous physiological processes that orchestrate individual cell activities toward the anatomical needs of an organism. Thus, the origin and maintenance of complex biological shape is a fundamental question for cell, developmental, and evolutionary biology, as well as for biomedicine. It has long been recognized that slow bioelectrical gradients can control cell behaviors and morphogenesis. Here, I review recent molecular data that implicate endogenous spatio‐temporal patterns of resting potentials among non‐excitable cells as instructive cues in embryogenesis, regeneration, and cancer. Functional data have implicated gradients of resting potential in processes such as limb regeneration, eye induction, craniofacial patterning, and head‐tail polarity, as well as in metastatic transformation and tumorigenesis. The genome is tightly linked to bioelectric signaling, via ion channel proteins that shape the gradients, downstream genes whose transcription is regulated by voltage, and transduction machinery that converts changes in bioelectric state to second‐messenger cascades. However, the data clearly indicate that bioelectric signaling is an autonomous layer of control not reducible to a biochemical or genetic account of cell state. The real‐time dynamics of bioelectric communication among cells are not fully captured by transcriptomic or proteomic analyses, and the necessary‐and‐sufficient triggers for specific changes in growth and form can be physiological states, while the underlying gene loci are free to diverge. The next steps in this exciting new field include the development of novel conceptual tools for understanding the anatomical semantics encoded in non‐neural bioelectrical networks, and of improved biophysical tools for reading and writing electrical state information into somatic tissues. Cracking the bioelectric code will have transformative implications for developmental biology, regenerative medicine, and synthetic bioengineering.

[1]  A. Sater,et al.  Analysis of growth factor signaling in embryos , 2006 .

[2]  D. Spray,et al.  Connexin and pannexin mediated cell-cell communication. , 2007, Neuron glia biology.

[3]  Michael Levin,et al.  A chemical genetics approach reveals H,K-ATPase-mediated membrane voltage is required for planarian head regeneration. , 2011, Chemistry & biology.

[4]  V. Zykov Spiral Waves in Two‐dimensional Excitable Media , 1990, Annals of the New York Academy of Sciences.

[5]  N. Spitzer,et al.  Spontaneous calcium influx and its roles in differentiation of spinal neurons in culture. , 1990, Developmental biology.

[6]  R. Shi,et al.  Three‐dimensional gradients of voltage during development of the nervous system as invisible coordinates for the establishment of embryonic pattern , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[7]  Dominique Debanne,et al.  Brain plasticity and ion channels , 2003, Journal of Physiology-Paris.

[8]  Andrew Adamatzky,et al.  Towards Arithmetic Circuits in Sub‐Excitable Chemical Media , 2011 .

[9]  David L. Kaplan,et al.  Role of Membrane Potential in the Regulation of Cell Proliferation and Differentiation , 2009, Stem Cell Reviews and Reports.

[10]  Jerzy Gorecki,et al.  Chemical Wave Based Programming in Reaction-Diffusion Systems , 2007, Int. J. Unconv. Comput..

[11]  A. Garfinkel,et al.  Spirals, Chaos, and New Mechanisms of Wave Propagation , 1997, Pacing and clinical electrophysiology : PACE.

[12]  C. Cone,et al.  Control of somatic cell mitosis by simulated changes in the transmembrane potential level. , 1971, Oncology.

[13]  Michael Levin,et al.  Modeling Planarian Regeneration: A Primer for Reverse-Engineering the Worm , 2012, PLoS Comput. Biol..

[14]  M. Mercola,et al.  Asymmetries in H+/K+-ATPase and Cell Membrane Potentials Comprise a Very Early Step in Left-Right Patterning , 2002, Cell.

[15]  M. Levin,et al.  Measuring resting membrane potential using the fluorescent voltage reporters DiBAC4(3) and CC2-DMPE. , 2012, Cold Spring Harbor protocols.

[16]  Dany S. Adams,et al.  Early, H+-V-ATPase-dependent proton flux is necessary for consistent left-right patterning of non-mammalian vertebrates , 2006, Development.

[17]  Y Schiffmann,et al.  An hypothesis: phosphorylation fields as the source of positional information and cell differentiation--(cAMP, ATP) as the universal morphogenetic Turing couple. , 1991, Progress in biophysics and molecular biology.

[18]  G. Hoge,et al.  Gap junction-mediated electrical transmission: regulatory mechanisms and plasticity. , 2013, Biochimica et biophysica acta.

[19]  T. Lepage,et al.  Reciprocal Signaling between the Ectoderm and a Mesendodermal Left-Right Organizer Directs Left-Right Determination in the Sea Urchin Embryo , 2012, PLoS genetics.

[20]  Bard Ermentrout,et al.  The neural origins of shell structure and pattern in aquatic mollusks , 2009, Proceedings of the National Academy of Sciences.

[21]  R. Nuccitelli,et al.  On electrical currents in development. , 1986, BioEssays : news and reviews in molecular, cellular and developmental biology.

[22]  R. Coombes,et al.  Voltage-Gated Sodium Channel Expression and Potentiation of Human Breast Cancer Metastasis , 2005, Clinical Cancer Research.

[23]  Min Zhao,et al.  Controlling cell behavior electrically: current views and future potential. , 2005, Physiological reviews.

[24]  Lance A Davidson,et al.  Physics and the canalization of morphogenesis: a grand challenge in organismal biology , 2011, Physical biology.

[25]  Teresa Adell,et al.  Planarian regeneration: achievements and future directions after 20 years of research. , 2009, The International journal of developmental biology.

[26]  Ryan D Morrie,et al.  V‐ATPase‐dependent ectodermal voltage and ph regionalization are required for craniofacial morphogenesis , 2011, Developmental dynamics : an official publication of the American Association of Anatomists.

[27]  Charles A. Vacanti,et al.  Stimulus-triggered fate conversion of somatic cells into pluripotency , 2014, Nature.

[28]  Min Zhao,et al.  Electrical fields in wound healing-An overriding signal that directs cell migration. , 2009, Seminars in cell & developmental biology.

[29]  Martin Tristani-Firouzi,et al.  Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome* , 2003, Journal of Biological Chemistry.

[30]  Michael Levin,et al.  Characterization of innexin gene expression and functional roles of gap-junctional communication in planarian regeneration. , 2005, Developmental biology.

[31]  Drew N. Robson,et al.  Supplementary Materials for Differential Diffusivity of Nodal and Lefty Underlies a Reaction-Diffusion Patterning System , 2012 .

[32]  Michael Levin,et al.  A linear-encoding model explains the variability of the target morphology in regeneration , 2014, Journal of The Royal Society Interface.

[33]  Takashi Gojobori,et al.  Long-range neural and gap junction protein-mediated cues control polarity during planarian regeneration. , 2010, Developmental biology.

[34]  F. Northrop,et al.  The Electro-Dynamic Theory of Life , 1935, The Quarterly Review of Biology.

[35]  Alejandro Sánchez Alvarado,et al.  Regeneration in the metazoans: why does it happen? , 2000 .

[36]  Harold M. Hastings,et al.  Memory in an Excitable Medium: A Mechanism for Spiral Wave Breakup in the Low-Excitability Limit , 1999 .

[37]  Christof Niehrs,et al.  On growth and form: a Cartesian coordinate system of Wnt and BMP signaling specifies bilaterian body axes , 2010, Development.

[38]  M. Dean Cancer as a complex developmental disorder--nineteenth Cornelius P. Rhoads Memorial Award Lecture. , 1998, Cancer Research.

[39]  N. Geard,et al.  Dynamical approaches to modeling developmental gene regulatory networks. , 2009, Birth defects research. Part C, Embryo today : reviews.

[40]  A B Bubenik,et al.  Trophic responses to trauma in growing antlers. , 1965, The Journal of experimental zoology.

[41]  Michael Levin,et al.  Morphogenetic fields in embryogenesis, regeneration, and cancer: Non-local control of complex patterning , 2012, Biosyst..

[42]  Michael Levin,et al.  Reprogramming cells and tissue patterning via bioelectrical pathways: molecular mechanisms and biomedical opportunities , 2013, Wiley interdisciplinary reviews. Systems biology and medicine.

[43]  L. Davidson Epithelial machines that shape the embryo. , 2012, Trends in cell biology.

[44]  Stillwell Ef,et al.  Stimulation of DNA synthesis in CNS neurones by sustained depolarisation. , 1973 .

[45]  R. Blakely,et al.  Serotonin Transporter Function Is an Early Step in Left-Right Patterning in Chick and Frog Embryos , 2005, Developmental Neuroscience.

[46]  Celeste M Nelson,et al.  Geometric control of tissue morphogenesis. , 2009, Biochimica et biophysica acta.

[47]  K. Hotary,et al.  Evidence of a role for endogenous electrical fields in chick embryo development. , 1992, Development.

[48]  R. Binggeli,et al.  Membrane potentials and sodium channels: hypotheses for growth regulation and cancer formation based on changes in sodium channels and gap junctions. , 1986, Journal of theoretical biology.

[49]  E. Marder Electrical Synapses: Rectification Demystified , 2009, Current Biology.

[50]  Kenneth D. Birnbaum,et al.  Slicing across Kingdoms: Regeneration in Plants and Animals , 2008, Cell.

[51]  J. C. Belmonte,et al.  Notch activity acts as a sensor for extracellular calcium during vertebrate left–right determination , 2004, Nature.

[52]  Michael Levin,et al.  Induction of Vertebrate Regeneration by a Transient Sodium Current , 2010, The Journal of Neuroscience.

[53]  J. Sharpe,et al.  Hox Genes Regulate Digit Patterning by Controlling the Wavelength of a Turing-Type Mechanism , 2012, Science.

[54]  Michael Levin,et al.  Bioelectric controls of cell proliferation: Ion channels, membrane voltage and the cell cycle , 2009, Cell cycle.

[55]  Carlos Gershenson,et al.  Guiding the self-organization of random Boolean networks , 2010, Theory in Biosciences.

[56]  M. Netsky,et al.  The Brain of the Planarian as the Ancestor of the Human Brain , 1985, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[57]  Min Zhao,et al.  Electrical signals control wound healing through phosphatidylinositol-3-OH kinase-γ and PTEN , 2006, Nature.

[58]  L. Beloussov,et al.  Morphomechanics: goals, basic experiments and models. , 2006, The International journal of developmental biology.

[59]  Suk-Ho Lee,et al.  Prolonged Membrane Depolarization Enhances Midbrain Dopamine Neuron Differentiation via Epigenetic Histone Modifications , 2011, Stem cells.

[60]  C. McCaig,et al.  Electrical dimensions in cell science , 2009, Journal of Cell Science.

[61]  M. Minden,et al.  The antiparasitic agent ivermectin induces chloride-dependent membrane hyperpolarization and cell death in leukemia cells. , 2010, Blood.

[62]  M. Levin,et al.  Endogenous voltage gradients as mediators of cell-cell communication: strategies for investigating bioelectrical signals during pattern formation , 2012, Cell and Tissue Research.

[63]  O. Crociani,et al.  Targeting ion channels in cancer: a novel frontier in antineoplastic therapy. , 2009, Current medicinal chemistry.

[64]  Jean M Harper,et al.  Voltage-gated Na+ channels confer invasive properties on human prostate cancer cells , 2004, Pflügers Archiv.

[65]  S. Mancuso From bioelectricity, via signaling, to behavioral actions , 2013 .

[66]  M. Levin Molecular bioelectricity in developmental biology: New tools and recent discoveries , 2012, BioEssays : news and reviews in molecular, cellular and developmental biology.

[67]  S. Hagiwara,et al.  The calcium channel , 1983, Trends in Neurosciences.

[68]  V. Ganapathy,et al.  Functional Identification of SLC5A8, a Tumor Suppressor Down-regulated in Colon Cancer, as a Na+-coupled Transporter for Short-chain Fatty Acids* , 2004, Journal of Biological Chemistry.

[69]  Gabriel S. Eichler,et al.  Cell fates as high-dimensional attractor states of a complex gene regulatory network. , 2005, Physical review letters.

[70]  D. Largaespada,et al.  The role of KCNQ1 in mouse and human gastrointestinal cancers , 2013, Oncogene.

[71]  M. Levin,et al.  Transmembrane potential of GlyCl-expressing instructor cells induces a neoplastic-like conversion of melanocytes via a serotonergic pathway , 2010, Disease Models & Mechanisms.

[72]  H. Rubin Cancer as a dynamic developmental disorder. , 1985, Cancer research.

[73]  L. Beloussov,et al.  Mechanically based generative laws of morphogenesis , 2008, Physical biology.

[74]  M. Zoghi Cardiac Memory: Do the Heart and the Brain Remember the Same? , 2004, Journal of Interventional Cardiac Electrophysiology.

[75]  Raoul Kopelman,et al.  "Nanosized voltmeter" enables cellular-wide electric field mapping. , 2007, Biophysical journal.

[76]  Michael Levin,et al.  General principles for measuring resting membrane potential and ion concentration using fluorescent bioelectricity reporters. , 2012, Cold Spring Harbor protocols.

[77]  E. Wanke,et al.  Electric fields at the plasma membrane level: a neglected element in the mechanisms of cell signalling. , 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.

[78]  Michael Levin,et al.  Bioelectric signaling regulates head and organ size during planarian regeneration , 2013, Development.

[79]  F. Calegari,et al.  Bioelectric State and Cell Cycle Control of Mammalian Neural Stem Cells , 2012, Stem cells international.

[80]  Subhabrata Sanyal,et al.  Modeling the genetic basis for human sleep disorders in Drosophila , 2013, Communicative & integrative biology.

[81]  M. Yamashita Fluctuations in nuclear envelope's potential mediate synchronization of early neural activity. , 2011, Biochemical and biophysical research communications.

[82]  P. Reddien,et al.  Fundamentals of planarian regeneration. , 2004, Annual review of cell and developmental biology.

[83]  D. Burr,et al.  Do Bone Cells Behave Like a Neuronal Network? , 2002, Calcified Tissue International.

[84]  Y. Schiffmann Self-organization in biology and development. , 1997, Progress in biophysics and molecular biology.

[85]  M. Brizzi,et al.  HERG potassium channels are constitutively expressed in primary human acute myeloid leukemias and regulate cell proliferation of normal and leukemic hemopoietic progenitors , 2002, Leukemia.

[86]  D. Kaplan,et al.  Depolarization alters phenotype, maintains plasticity of predifferentiated mesenchymal stem cells. , 2013, Tissue engineering. Part A.

[87]  D. Roden,et al.  Voltage-Gated Sodium Channels Are Required for Heart Development in Zebrafish , 2010, Circulation research.

[88]  Dany S. Adams,et al.  H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration , 2007, Development.

[89]  Elmer Julius Lund,et al.  Bioelectric fields and growth , 1947 .

[90]  M. Levin,et al.  Resting potential, oncogene-induced tumorigenesis, and metastasis: the bioelectric basis of cancer in vivo , 2012, Physical biology.

[91]  B. Reid,et al.  Non-invasive measurement of bioelectric currents with a vibrating probe , 2007, Nature Protocols.

[92]  Stimulation of DNA synthesis in CNS neurones by sustained depolarisation. , 1973, Nature: New biology.

[93]  Zhiguo Wang Roles of K+ channels in regulating tumour cell proliferation and apoptosis , 2004, Pflügers Archiv.

[94]  Kunihiko Kaneko,et al.  Dynamical systems basis of metamorphosis: diversity and plasticity of cellular states in reaction diffusion network. , 2003, Journal of theoretical biology.

[95]  Stefan R. Pulver,et al.  Spike integration and cellular memory in a rhythmic network from Na+/K+ pump current dynamics , 2009, Nature Neuroscience.

[96]  N. Barkai,et al.  Scaling of morphogen gradients. , 2011, Current opinion in genetics & development.

[97]  Michael Levin,et al.  An automated training paradigm reveals long-term memory in planarians and its persistence through head regeneration , 2013, Journal of Experimental Biology.

[98]  L. Gentile,et al.  The planarian flatworm: an in vivo model for stem cell biology and nervous system regeneration , 2010, Disease Models & Mechanisms.

[99]  D. Debanne,et al.  Long-term plasticity of intrinsic excitability: learning rules and mechanisms. , 2003, Learning & memory.

[100]  Michael Levin,et al.  Transmembrane voltage potential controls embryonic eye patterning in Xenopus laevis , 2012, Development.

[101]  H. Seno,et al.  A Mathematical Modelling for the Cheliped Regeneration with Handedness in Fiddler Crab , 2007, Bulletin of mathematical biology.

[102]  Y. Okamura,et al.  Voltage-sensing phosphatase: its molecular relationship with PTEN. , 2011, Physiology.

[103]  Julio A. Hernández,et al.  ENaC contribution to epithelial wound healing is independent of the healing mode and of any increased expression in the channel , 2013, Cell and Tissue Research.

[104]  L. Ptáček,et al.  An inwardly rectifying K+ channel is required for patterning , 2012, Development.

[105]  Yasushi Okamura,et al.  Phosphoinositide phosphatase activity coupled to an intrinsic voltage sensor , 2005, Nature.

[106]  David L. Kaplan,et al.  Membrane Potential Controls Adipogenic and Osteogenic Differentiation of Mesenchymal Stem Cells , 2008, PloS one.

[107]  N. Navaratnam,et al.  Potassium channel KCNA1 modulates oncogene-induced senescence and transformation. , 2013, Cancer research.

[108]  J O Bustamante,et al.  Electrical dimension of the nuclear envelope. , 2001, Physiological reviews.

[109]  Michael Levin,et al.  Transducing Bioelectric Signals into Epigenetic Pathways During Tadpole Tail Regeneration , 2012, Anatomical record.

[110]  C. Martyniuk,et al.  Genome wide analysis of Silurana (Xenopus) tropicalis development reveals dynamic expression using network enrichment analysis , 2013, Mechanisms of Development.

[111]  Michael Levin,et al.  The wisdom of the body: future techniques and approaches to morphogenetic fields in regenerative medicine, developmental biology and cancer. , 2011, Regenerative medicine.

[112]  R. Nuccitelli,et al.  Electrical controls of development. , 1977, Annual review of biophysics and bioengineering.

[113]  M. Levin,et al.  Transmembrane voltage potential is an essential cellular parameter for the detection and control of tumor development in a Xenopus model , 2013, Disease Models & Mechanisms.

[114]  L. Pardo,et al.  Potassium channels as tumour markers , 2006, FEBS letters.

[115]  C. McCaig,et al.  Calcium channel subtypes and intracellular calcium stores modulate electric field-stimulated and -oriented nerve growth. , 1995, Developmental biology.

[116]  Karl Deisseroth,et al.  Tracking Stem Cell Differentiation in the Setting of Automated Optogenetic Stimulation , 2011, Stem cells.

[117]  A. Becchetti,et al.  Targeting ion channels in leukemias: a new challenge for treatment. , 2012, Current medicinal chemistry.

[118]  Michael Levin,et al.  Large-scale biophysics: ion flows and regeneration. , 2007, Trends in cell biology.

[119]  George Oster,et al.  Emergent complexity in simple neural systems , 2009, Communicative & integrative biology.

[120]  Stephen L. Johnson,et al.  Bioelectric Signaling Regulates Size in Zebrafish Fins , 2014, PLoS genetics.

[121]  Jin Pu,et al.  GSK-3β is essential for physiological electric field-directed Golgi polarization and optimal electrotaxis , 2011, Cellular and Molecular Life Sciences.

[122]  William J. Brackenbury,et al.  Membrane potential and cancer progression , 2013, Front. Physiol..

[123]  A. Jacobson,et al.  The effects of regeneration upon retention of a conditioned response in the planarian. , 1959, Journal of comparative and physiological psychology.

[124]  Feliksas F. Bukauskas,et al.  Heterotypic gap junction channels as voltage-sensitive valves for intercellular signaling , 2009, Proceedings of the National Academy of Sciences.

[125]  D. Adams,et al.  A new tool for tissue engineers: ions as regulators of morphogenesis during development and regeneration. , 2008, Tissue engineering. Part A.

[126]  C. Pullar The physiology of bioelectricity in development, tissue regeneration, and cancer , 2016 .