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Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form
Planaria are complex metazoans that repair damage to their bodies and cease remodeling when a correct anatomy has been achieved. This model system offers a unique opportunity to understand how large‐scale anatomical homeostasis emerges from the activities of individual cells. Much progress has been...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895326/ https://www.ncbi.nlm.nih.gov/pubmed/27499881 http://dx.doi.org/10.1002/reg2.54 |
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author | Durant, Fallon Lobo, Daniel Hammelman, Jennifer Levin, Michael |
author_facet | Durant, Fallon Lobo, Daniel Hammelman, Jennifer Levin, Michael |
author_sort | Durant, Fallon |
collection | PubMed |
description | Planaria are complex metazoans that repair damage to their bodies and cease remodeling when a correct anatomy has been achieved. This model system offers a unique opportunity to understand how large‐scale anatomical homeostasis emerges from the activities of individual cells. Much progress has been made on the molecular genetics of stem cell activity in planaria. However, recent data also indicate that the global pattern is regulated by physiological circuits composed of ionic and neurotransmitter signaling. Here, we overview the multi‐scale problem of understanding pattern regulation in planaria, with specific focus on bioelectric signaling via ion channels and gap junctions (electrical synapses), and computational efforts to extract explanatory models from functional and molecular data on regeneration. We present a perspective that interprets results in this fascinating field using concepts from dynamical systems theory and computational neuroscience. Serving as a tractable nexus between genetic, physiological, and computational approaches to pattern regulation, planarian pattern homeostasis harbors many deep insights for regenerative medicine, evolutionary biology, and engineering. |
format | Online Article Text |
id | pubmed-4895326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48953262016-08-05 Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form Durant, Fallon Lobo, Daniel Hammelman, Jennifer Levin, Michael Regeneration (Oxf) Review Planaria are complex metazoans that repair damage to their bodies and cease remodeling when a correct anatomy has been achieved. This model system offers a unique opportunity to understand how large‐scale anatomical homeostasis emerges from the activities of individual cells. Much progress has been made on the molecular genetics of stem cell activity in planaria. However, recent data also indicate that the global pattern is regulated by physiological circuits composed of ionic and neurotransmitter signaling. Here, we overview the multi‐scale problem of understanding pattern regulation in planaria, with specific focus on bioelectric signaling via ion channels and gap junctions (electrical synapses), and computational efforts to extract explanatory models from functional and molecular data on regeneration. We present a perspective that interprets results in this fascinating field using concepts from dynamical systems theory and computational neuroscience. Serving as a tractable nexus between genetic, physiological, and computational approaches to pattern regulation, planarian pattern homeostasis harbors many deep insights for regenerative medicine, evolutionary biology, and engineering. John Wiley and Sons Inc. 2016-04-28 /pmc/articles/PMC4895326/ /pubmed/27499881 http://dx.doi.org/10.1002/reg2.54 Text en © 2016 The Authors. Regeneration published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Durant, Fallon Lobo, Daniel Hammelman, Jennifer Levin, Michael Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form |
title | Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form |
title_full | Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form |
title_fullStr | Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form |
title_full_unstemmed | Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form |
title_short | Physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form |
title_sort | physiological controls of large‐scale patterning in planarian regeneration: a molecular and computational perspective on growth and form |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895326/ https://www.ncbi.nlm.nih.gov/pubmed/27499881 http://dx.doi.org/10.1002/reg2.54 |
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