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Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation

Patterns of resting potential in non-excitable cells of living tissue are now known to be instructive signals for pattern formation during embryogenesis, regeneration and cancer suppression. The development of molecular-level techniques for tracking ion flows and functionally manipulating the activi...

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Autores principales: Tseng, AiSun, Levin, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689572/
https://www.ncbi.nlm.nih.gov/pubmed/23802040
http://dx.doi.org/10.4161/cib.22595
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author Tseng, AiSun
Levin, Michael
author_facet Tseng, AiSun
Levin, Michael
author_sort Tseng, AiSun
collection PubMed
description Patterns of resting potential in non-excitable cells of living tissue are now known to be instructive signals for pattern formation during embryogenesis, regeneration and cancer suppression. The development of molecular-level techniques for tracking ion flows and functionally manipulating the activity of ion channels and pumps has begun to reveal the mechanisms by which voltage gradients regulate cell behaviors and the assembly of complex large-scale structures. A recent paper demonstrated that a specific voltage range is necessary for demarcation of eye fields in the frog embryo. Remarkably, artificially setting other somatic cells to the eye-specific voltage range resulted in formation of eyes in aberrant locations, including tissues that are not in the normal anterior ectoderm lineage: eyes could be formed in the gut, on the tail, or in the lateral plate mesoderm. These data challenge the existing models of eye fate restriction and tissue competence maps, and suggest the presence of a bioelectric code—a mapping of physiological properties to anatomical outcomes. This Addendum summarizes the current state of knowledge in developmental bioelectricity, proposes three possible interpretations of the bioelectric code that functionally maps physiological states to anatomical outcomes, and highlights the biggest open questions in this field. We also suggest a speculative hypothesis at the intersection of cognitive science and developmental biology: that bioelectrical signaling among non-excitable cells coupled by gap junctions simulates neural network-like dynamics, and underlies the information processing functions required by complex pattern formation in vivo. Understanding and learning to control the information stored in physiological networks will have transformative implications for developmental biology, regenerative medicine and synthetic bioengineering.
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spelling pubmed-36895722013-06-25 Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation Tseng, AiSun Levin, Michael Commun Integr Biol Article Addendum Patterns of resting potential in non-excitable cells of living tissue are now known to be instructive signals for pattern formation during embryogenesis, regeneration and cancer suppression. The development of molecular-level techniques for tracking ion flows and functionally manipulating the activity of ion channels and pumps has begun to reveal the mechanisms by which voltage gradients regulate cell behaviors and the assembly of complex large-scale structures. A recent paper demonstrated that a specific voltage range is necessary for demarcation of eye fields in the frog embryo. Remarkably, artificially setting other somatic cells to the eye-specific voltage range resulted in formation of eyes in aberrant locations, including tissues that are not in the normal anterior ectoderm lineage: eyes could be formed in the gut, on the tail, or in the lateral plate mesoderm. These data challenge the existing models of eye fate restriction and tissue competence maps, and suggest the presence of a bioelectric code—a mapping of physiological properties to anatomical outcomes. This Addendum summarizes the current state of knowledge in developmental bioelectricity, proposes three possible interpretations of the bioelectric code that functionally maps physiological states to anatomical outcomes, and highlights the biggest open questions in this field. We also suggest a speculative hypothesis at the intersection of cognitive science and developmental biology: that bioelectrical signaling among non-excitable cells coupled by gap junctions simulates neural network-like dynamics, and underlies the information processing functions required by complex pattern formation in vivo. Understanding and learning to control the information stored in physiological networks will have transformative implications for developmental biology, regenerative medicine and synthetic bioengineering. Landes Bioscience 2013-01-01 2013-01-01 /pmc/articles/PMC3689572/ /pubmed/23802040 http://dx.doi.org/10.4161/cib.22595 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Article Addendum
Tseng, AiSun
Levin, Michael
Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation
title Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation
title_full Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation
title_fullStr Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation
title_full_unstemmed Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation
title_short Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation
title_sort cracking the bioelectric code: probing endogenous ionic controls of pattern formation
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689572/
https://www.ncbi.nlm.nih.gov/pubmed/23802040
http://dx.doi.org/10.4161/cib.22595
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