Cargando…

A dual-flow RootChip enables quantification of bi-directional calcium signaling in primary roots

One sentence summary: Bi-directional-dual-flow-RootChip to track calcium signatures in Arabidopsis primary roots responding to osmotic stress. Plant growth and survival is fundamentally linked with the ability to detect and respond to abiotic and biotic factors. Cytosolic free calcium (Ca(2+)) is a...

Descripción completa

Detalles Bibliográficos
Autores principales: Allan, Claudia, Tayagui, Ayelen, Hornung, Rainer, Nock, Volker, Meisrimler, Claudia-Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9871814/
https://www.ncbi.nlm.nih.gov/pubmed/36704158
http://dx.doi.org/10.3389/fpls.2022.1040117
_version_ 1784877265278992384
author Allan, Claudia
Tayagui, Ayelen
Hornung, Rainer
Nock, Volker
Meisrimler, Claudia-Nicole
author_facet Allan, Claudia
Tayagui, Ayelen
Hornung, Rainer
Nock, Volker
Meisrimler, Claudia-Nicole
author_sort Allan, Claudia
collection PubMed
description One sentence summary: Bi-directional-dual-flow-RootChip to track calcium signatures in Arabidopsis primary roots responding to osmotic stress. Plant growth and survival is fundamentally linked with the ability to detect and respond to abiotic and biotic factors. Cytosolic free calcium (Ca(2+)) is a key messenger in signal transduction pathways associated with a variety of stresses, including mechanical, osmotic stress and the plants’ innate immune system. These stresses trigger an increase in cytosolic Ca(2+) and thus initiate a signal transduction cascade, contributing to plant stress adaptation. Here we combine fluorescent G-CaMP3 Arabidopsis thaliana sensor lines to visualise Ca(2+) signals in the primary root of 9-day old plants with an optimised dual-flow RootChip (dfRC). The enhanced polydimethylsiloxane (PDMS) bi-directional-dual-flow-RootChip (bi-dfRC) reported here adds two adjacent inlet channels at the base of the observation chamber, allowing independent or asymmetric chemical stimulation at either the root differentiation zone or tip. Observations confirm distinct early spatio-temporal patterns of salinity (sodium chloride, NaCl) and drought (polyethylene glycol, PEG)-induced Ca(2+) signals throughout different cell types dependent on the first contact site. Furthermore, we show that the primary signal always dissociates away from initially stimulated cells. The observed early signaling events induced by NaCl and PEG are surprisingly complex and differ from long-term changes in cytosolic Ca(2+) reported in roots. Bi-dfRC microfluidic devices will provide a novel approach to challenge plant roots with different conditions simultaneously, while observing bi-directionality of signals. Future applications include combining the bi-dfRC with H(2)O(2) and redox sensor lines to test root systemic signaling responses to biotic and abiotic factors.
format Online
Article
Text
id pubmed-9871814
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-98718142023-01-25 A dual-flow RootChip enables quantification of bi-directional calcium signaling in primary roots Allan, Claudia Tayagui, Ayelen Hornung, Rainer Nock, Volker Meisrimler, Claudia-Nicole Front Plant Sci Plant Science One sentence summary: Bi-directional-dual-flow-RootChip to track calcium signatures in Arabidopsis primary roots responding to osmotic stress. Plant growth and survival is fundamentally linked with the ability to detect and respond to abiotic and biotic factors. Cytosolic free calcium (Ca(2+)) is a key messenger in signal transduction pathways associated with a variety of stresses, including mechanical, osmotic stress and the plants’ innate immune system. These stresses trigger an increase in cytosolic Ca(2+) and thus initiate a signal transduction cascade, contributing to plant stress adaptation. Here we combine fluorescent G-CaMP3 Arabidopsis thaliana sensor lines to visualise Ca(2+) signals in the primary root of 9-day old plants with an optimised dual-flow RootChip (dfRC). The enhanced polydimethylsiloxane (PDMS) bi-directional-dual-flow-RootChip (bi-dfRC) reported here adds two adjacent inlet channels at the base of the observation chamber, allowing independent or asymmetric chemical stimulation at either the root differentiation zone or tip. Observations confirm distinct early spatio-temporal patterns of salinity (sodium chloride, NaCl) and drought (polyethylene glycol, PEG)-induced Ca(2+) signals throughout different cell types dependent on the first contact site. Furthermore, we show that the primary signal always dissociates away from initially stimulated cells. The observed early signaling events induced by NaCl and PEG are surprisingly complex and differ from long-term changes in cytosolic Ca(2+) reported in roots. Bi-dfRC microfluidic devices will provide a novel approach to challenge plant roots with different conditions simultaneously, while observing bi-directionality of signals. Future applications include combining the bi-dfRC with H(2)O(2) and redox sensor lines to test root systemic signaling responses to biotic and abiotic factors. Frontiers Media S.A. 2023-01-10 /pmc/articles/PMC9871814/ /pubmed/36704158 http://dx.doi.org/10.3389/fpls.2022.1040117 Text en Copyright © 2023 Allan, Tayagui, Hornung, Nock and Meisrimler https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Allan, Claudia
Tayagui, Ayelen
Hornung, Rainer
Nock, Volker
Meisrimler, Claudia-Nicole
A dual-flow RootChip enables quantification of bi-directional calcium signaling in primary roots
title A dual-flow RootChip enables quantification of bi-directional calcium signaling in primary roots
title_full A dual-flow RootChip enables quantification of bi-directional calcium signaling in primary roots
title_fullStr A dual-flow RootChip enables quantification of bi-directional calcium signaling in primary roots
title_full_unstemmed A dual-flow RootChip enables quantification of bi-directional calcium signaling in primary roots
title_short A dual-flow RootChip enables quantification of bi-directional calcium signaling in primary roots
title_sort dual-flow rootchip enables quantification of bi-directional calcium signaling in primary roots
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9871814/
https://www.ncbi.nlm.nih.gov/pubmed/36704158
http://dx.doi.org/10.3389/fpls.2022.1040117
work_keys_str_mv AT allanclaudia adualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT tayaguiayelen adualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT hornungrainer adualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT nockvolker adualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT meisrimlerclaudianicole adualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT allanclaudia dualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT tayaguiayelen dualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT hornungrainer dualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT nockvolker dualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots
AT meisrimlerclaudianicole dualflowrootchipenablesquantificationofbidirectionalcalciumsignalinginprimaryroots