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Cnidocyte discharge is regulated by light and opsin-mediated phototransduction

BACKGROUND: Cnidocytes, the eponymous cell type of the Cnidaria, facilitate both sensory and secretory functions and are among the most complex animal cell types known. In addition to their structural complexity, cnidocytes display complex sensory attributes, integrating both chemical and mechanical...

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Autores principales: Plachetzki, David C, Fong, Caitlin R, Oakley, Todd H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329406/
https://www.ncbi.nlm.nih.gov/pubmed/22390726
http://dx.doi.org/10.1186/1741-7007-10-17
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author Plachetzki, David C
Fong, Caitlin R
Oakley, Todd H
author_facet Plachetzki, David C
Fong, Caitlin R
Oakley, Todd H
author_sort Plachetzki, David C
collection PubMed
description BACKGROUND: Cnidocytes, the eponymous cell type of the Cnidaria, facilitate both sensory and secretory functions and are among the most complex animal cell types known. In addition to their structural complexity, cnidocytes display complex sensory attributes, integrating both chemical and mechanical cues from the environment into their discharge behavior. Despite more than a century of work aimed at understanding the sensory biology of cnidocytes, the specific sensory receptor genes that regulate their function remain unknown. RESULTS: Here we report that light also regulates cnidocyte function. We show that non-cnidocyte neurons located in battery complexes of the freshwater polyp Hydra magnipapillata specifically express opsin, cyclic nucleotide gated (CNG) ion channel and arrestin, which are all known components of bilaterian phototransduction cascades. We infer from behavioral trials that different light intensities elicit significant effects on cnidocyte discharge propensity. Harpoon-like stenotele cnidocytes show a pronounced diminution of discharge behavior under bright light conditions as compared to dim light. Further, we show that suppression of firing by bright light is ablated by cis-diltiazem, a specific inhibitor of CNG ion channels. CONCLUSIONS: Our results implicate an ancient opsin-mediated phototransduction pathway and a previously unknown layer of sensory complexity in the control of cnidocyte discharge. These findings also suggest a molecular mechanism for the regulation of other cnidarian behaviors that involve both photosensitivity and cnidocyte function, including diurnal feeding repertoires and/or substrate-based locomotion. More broadly, our findings highlight one novel, non-visual function for opsin-mediated phototransduction in a cnidarian, the origins of which might have preceded the evolution of cnidarian eyes.
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spelling pubmed-33294062012-04-19 Cnidocyte discharge is regulated by light and opsin-mediated phototransduction Plachetzki, David C Fong, Caitlin R Oakley, Todd H BMC Biol Research Article BACKGROUND: Cnidocytes, the eponymous cell type of the Cnidaria, facilitate both sensory and secretory functions and are among the most complex animal cell types known. In addition to their structural complexity, cnidocytes display complex sensory attributes, integrating both chemical and mechanical cues from the environment into their discharge behavior. Despite more than a century of work aimed at understanding the sensory biology of cnidocytes, the specific sensory receptor genes that regulate their function remain unknown. RESULTS: Here we report that light also regulates cnidocyte function. We show that non-cnidocyte neurons located in battery complexes of the freshwater polyp Hydra magnipapillata specifically express opsin, cyclic nucleotide gated (CNG) ion channel and arrestin, which are all known components of bilaterian phototransduction cascades. We infer from behavioral trials that different light intensities elicit significant effects on cnidocyte discharge propensity. Harpoon-like stenotele cnidocytes show a pronounced diminution of discharge behavior under bright light conditions as compared to dim light. Further, we show that suppression of firing by bright light is ablated by cis-diltiazem, a specific inhibitor of CNG ion channels. CONCLUSIONS: Our results implicate an ancient opsin-mediated phototransduction pathway and a previously unknown layer of sensory complexity in the control of cnidocyte discharge. These findings also suggest a molecular mechanism for the regulation of other cnidarian behaviors that involve both photosensitivity and cnidocyte function, including diurnal feeding repertoires and/or substrate-based locomotion. More broadly, our findings highlight one novel, non-visual function for opsin-mediated phototransduction in a cnidarian, the origins of which might have preceded the evolution of cnidarian eyes. BioMed Central 2012-03-05 /pmc/articles/PMC3329406/ /pubmed/22390726 http://dx.doi.org/10.1186/1741-7007-10-17 Text en Copyright ©2012 Plachetzki et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Plachetzki, David C
Fong, Caitlin R
Oakley, Todd H
Cnidocyte discharge is regulated by light and opsin-mediated phototransduction
title Cnidocyte discharge is regulated by light and opsin-mediated phototransduction
title_full Cnidocyte discharge is regulated by light and opsin-mediated phototransduction
title_fullStr Cnidocyte discharge is regulated by light and opsin-mediated phototransduction
title_full_unstemmed Cnidocyte discharge is regulated by light and opsin-mediated phototransduction
title_short Cnidocyte discharge is regulated by light and opsin-mediated phototransduction
title_sort cnidocyte discharge is regulated by light and opsin-mediated phototransduction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329406/
https://www.ncbi.nlm.nih.gov/pubmed/22390726
http://dx.doi.org/10.1186/1741-7007-10-17
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