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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-6881696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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