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Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap
Plants do not have neurons but operate transmembrane ion channels and can get electrical excited by physical and chemical clues. Among them the Venus flytrap is characterized by its peculiar hapto-electric signaling. When insects collide with trigger hairs emerging the trap inner surface, the mechan...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857258/ https://www.ncbi.nlm.nih.gov/pubmed/35181728 http://dx.doi.org/10.1038/s41598-022-06915-z |
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author | Scherzer, Sönke Huang, Shouguang Iosip, Anda Kreuzer, Ines Yokawa, Ken AL-Rasheid, Khaled A. S. Heckmann, Manfred Hedrich, Rainer |
author_facet | Scherzer, Sönke Huang, Shouguang Iosip, Anda Kreuzer, Ines Yokawa, Ken AL-Rasheid, Khaled A. S. Heckmann, Manfred Hedrich, Rainer |
author_sort | Scherzer, Sönke |
collection | PubMed |
description | Plants do not have neurons but operate transmembrane ion channels and can get electrical excited by physical and chemical clues. Among them the Venus flytrap is characterized by its peculiar hapto-electric signaling. When insects collide with trigger hairs emerging the trap inner surface, the mechanical stimulus within the mechanosensory organ is translated into a calcium signal and an action potential (AP). Here we asked how the Ca(2+) wave and AP is initiated in the trigger hair and how it is feed into systemic trap calcium-electrical networks. When Dionaea muscipula trigger hairs matures and develop hapto-electric excitability the mechanosensitive anion channel DmMSL10/FLYC1 and voltage dependent SKOR type Shaker K(+) channel are expressed in the sheering stress sensitive podium. The podium of the trigger hair is interface to the flytrap’s prey capture and processing networks. In the excitable state touch stimulation of the trigger hair evokes a rise in the podium Ca(2+) first and before the calcium signal together with an action potential travel all over the trap surface. In search for podium ion channels and pumps mediating touch induced Ca(2+) transients, we, in mature trigger hairs firing fast Ca(2+) signals and APs, found OSCA1.7 and GLR3.6 type Ca(2+) channels and ACA2/10 Ca(2+) pumps specifically expressed in the podium. Like trigger hair stimulation, glutamate application to the trap directly evoked a propagating Ca(2+) and electrical event. Given that anesthetics affect K(+) channels and glutamate receptors in the animal system we exposed flytraps to an ether atmosphere. As result propagation of touch and glutamate induced Ca(2+) and AP long-distance signaling got suppressed, while the trap completely recovered excitability when ether was replaced by fresh air. In line with ether targeting a calcium channel addressing a Ca(2+) activated anion channel the AP amplitude declined before the electrical signal ceased completely. Ether in the mechanosensory organ did neither prevent the touch induction of a calcium signal nor this post stimulus decay. This finding indicates that ether prevents the touch activated, glr3.6 expressing base of the trigger hair to excite the capture organ. |
format | Online Article Text |
id | pubmed-8857258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88572582022-02-22 Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap Scherzer, Sönke Huang, Shouguang Iosip, Anda Kreuzer, Ines Yokawa, Ken AL-Rasheid, Khaled A. S. Heckmann, Manfred Hedrich, Rainer Sci Rep Article Plants do not have neurons but operate transmembrane ion channels and can get electrical excited by physical and chemical clues. Among them the Venus flytrap is characterized by its peculiar hapto-electric signaling. When insects collide with trigger hairs emerging the trap inner surface, the mechanical stimulus within the mechanosensory organ is translated into a calcium signal and an action potential (AP). Here we asked how the Ca(2+) wave and AP is initiated in the trigger hair and how it is feed into systemic trap calcium-electrical networks. When Dionaea muscipula trigger hairs matures and develop hapto-electric excitability the mechanosensitive anion channel DmMSL10/FLYC1 and voltage dependent SKOR type Shaker K(+) channel are expressed in the sheering stress sensitive podium. The podium of the trigger hair is interface to the flytrap’s prey capture and processing networks. In the excitable state touch stimulation of the trigger hair evokes a rise in the podium Ca(2+) first and before the calcium signal together with an action potential travel all over the trap surface. In search for podium ion channels and pumps mediating touch induced Ca(2+) transients, we, in mature trigger hairs firing fast Ca(2+) signals and APs, found OSCA1.7 and GLR3.6 type Ca(2+) channels and ACA2/10 Ca(2+) pumps specifically expressed in the podium. Like trigger hair stimulation, glutamate application to the trap directly evoked a propagating Ca(2+) and electrical event. Given that anesthetics affect K(+) channels and glutamate receptors in the animal system we exposed flytraps to an ether atmosphere. As result propagation of touch and glutamate induced Ca(2+) and AP long-distance signaling got suppressed, while the trap completely recovered excitability when ether was replaced by fresh air. In line with ether targeting a calcium channel addressing a Ca(2+) activated anion channel the AP amplitude declined before the electrical signal ceased completely. Ether in the mechanosensory organ did neither prevent the touch induction of a calcium signal nor this post stimulus decay. This finding indicates that ether prevents the touch activated, glr3.6 expressing base of the trigger hair to excite the capture organ. Nature Publishing Group UK 2022-02-18 /pmc/articles/PMC8857258/ /pubmed/35181728 http://dx.doi.org/10.1038/s41598-022-06915-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Scherzer, Sönke Huang, Shouguang Iosip, Anda Kreuzer, Ines Yokawa, Ken AL-Rasheid, Khaled A. S. Heckmann, Manfred Hedrich, Rainer Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap |
title | Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap |
title_full | Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap |
title_fullStr | Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap |
title_full_unstemmed | Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap |
title_short | Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap |
title_sort | ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the venus flytrap |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857258/ https://www.ncbi.nlm.nih.gov/pubmed/35181728 http://dx.doi.org/10.1038/s41598-022-06915-z |
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