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Regenerative Adaptation to Electrochemical Perturbation in Planaria: A Molecular Analysis of Physiological Plasticity

Anatomical homeostasis results from dynamic interactions between gene expression, physiology, and the external environment. Owing to its complexity, this cellular and organism-level phenotypic plasticity is still poorly understood. We establish planarian regeneration as a model for acquired toleranc...

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Autores principales: Emmons-Bell, Maya, Durant, Fallon, Tung, Angela, Pietak, Alexis, Miller, Kelsie, Kane, Anna, Martyniuk, Christopher J., Davidian, Devon, Morokuma, Junji, Levin, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881696/
https://www.ncbi.nlm.nih.gov/pubmed/31765995
http://dx.doi.org/10.1016/j.isci.2019.11.014
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author Emmons-Bell, Maya
Durant, Fallon
Tung, Angela
Pietak, Alexis
Miller, Kelsie
Kane, Anna
Martyniuk, Christopher J.
Davidian, Devon
Morokuma, Junji
Levin, Michael
author_facet Emmons-Bell, Maya
Durant, Fallon
Tung, Angela
Pietak, Alexis
Miller, Kelsie
Kane, Anna
Martyniuk, Christopher J.
Davidian, Devon
Morokuma, Junji
Levin, Michael
author_sort Emmons-Bell, Maya
collection PubMed
description Anatomical homeostasis results from dynamic interactions between gene expression, physiology, and the external environment. Owing to its complexity, this cellular and organism-level phenotypic plasticity is still poorly understood. We establish planarian regeneration as a model for acquired tolerance to environments that alter endogenous physiology. Exposure to barium chloride (BaCl(2)) results in a rapid degeneration of anterior tissue in Dugesia japonica. Remarkably, continued exposure to fresh solution of BaCl(2) results in regeneration of heads that are insensitive to BaCl(2). RNA-seq revealed transcriptional changes in BaCl(2)-adapted heads that suggests a model of adaptation to excitotoxicity. Loss-of-function experiments confirmed several predictions: blockage of chloride and calcium channels allowed heads to survive initial BaCl(2) exposure, inducing adaptation without prior exposure, whereas blockade of TRPM channels reversed adaptation. Such highly adaptive plasticity may represent an attractive target for biomedical strategies in a wide range of applications beyond its immediate relevance to excitotoxicity preconditioning.
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spelling pubmed-68816962019-12-03 Regenerative Adaptation to Electrochemical Perturbation in Planaria: A Molecular Analysis of Physiological Plasticity Emmons-Bell, Maya Durant, Fallon Tung, Angela Pietak, Alexis Miller, Kelsie Kane, Anna Martyniuk, Christopher J. Davidian, Devon Morokuma, Junji Levin, Michael iScience Article Anatomical homeostasis results from dynamic interactions between gene expression, physiology, and the external environment. Owing to its complexity, this cellular and organism-level phenotypic plasticity is still poorly understood. We establish planarian regeneration as a model for acquired tolerance to environments that alter endogenous physiology. Exposure to barium chloride (BaCl(2)) results in a rapid degeneration of anterior tissue in Dugesia japonica. Remarkably, continued exposure to fresh solution of BaCl(2) results in regeneration of heads that are insensitive to BaCl(2). RNA-seq revealed transcriptional changes in BaCl(2)-adapted heads that suggests a model of adaptation to excitotoxicity. Loss-of-function experiments confirmed several predictions: blockage of chloride and calcium channels allowed heads to survive initial BaCl(2) exposure, inducing adaptation without prior exposure, whereas blockade of TRPM channels reversed adaptation. Such highly adaptive plasticity may represent an attractive target for biomedical strategies in a wide range of applications beyond its immediate relevance to excitotoxicity preconditioning. Elsevier 2019-11-09 /pmc/articles/PMC6881696/ /pubmed/31765995 http://dx.doi.org/10.1016/j.isci.2019.11.014 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Emmons-Bell, Maya
Durant, Fallon
Tung, Angela
Pietak, Alexis
Miller, Kelsie
Kane, Anna
Martyniuk, Christopher J.
Davidian, Devon
Morokuma, Junji
Levin, Michael
Regenerative Adaptation to Electrochemical Perturbation in Planaria: A Molecular Analysis of Physiological Plasticity
title Regenerative Adaptation to Electrochemical Perturbation in Planaria: A Molecular Analysis of Physiological Plasticity
title_full Regenerative Adaptation to Electrochemical Perturbation in Planaria: A Molecular Analysis of Physiological Plasticity
title_fullStr Regenerative Adaptation to Electrochemical Perturbation in Planaria: A Molecular Analysis of Physiological Plasticity
title_full_unstemmed Regenerative Adaptation to Electrochemical Perturbation in Planaria: A Molecular Analysis of Physiological Plasticity
title_short Regenerative Adaptation to Electrochemical Perturbation in Planaria: A Molecular Analysis of Physiological Plasticity
title_sort regenerative adaptation to electrochemical perturbation in planaria: a molecular analysis of physiological plasticity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881696/
https://www.ncbi.nlm.nih.gov/pubmed/31765995
http://dx.doi.org/10.1016/j.isci.2019.11.014
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