A tension-adhesion feedback loop in plant epidermis
Mechanical forces have emerged as coordinating signals for most cell functions. Yet, because forces are invisible, mapping tensile stress patterns in tissues remains a major challenge in all kingdoms. Here we take advantage of the adhesion defects in the Arabidopsis mutant quasimodo1 (qua1) to deduc...
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doaj-ee999ca0f4034a24b9ec3e9aeb900f142021-05-05T15:49:01ZengeLife Sciences Publications LtdeLife2050-084X2018-04-01710.7554/eLife.34460A tension-adhesion feedback loop in plant epidermisStéphane Verger0https://orcid.org/0000-0003-3643-3978Yuchen Long1Arezki Boudaoud2Olivier Hamant3https://orcid.org/0000-0001-6906-6620Laboratoire de Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRA, Lyon, FranceLaboratoire de Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRA, Lyon, FranceLaboratoire de Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRA, Lyon, FranceLaboratoire de Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRA, Lyon, FranceMechanical forces have emerged as coordinating signals for most cell functions. Yet, because forces are invisible, mapping tensile stress patterns in tissues remains a major challenge in all kingdoms. Here we take advantage of the adhesion defects in the Arabidopsis mutant quasimodo1 (qua1) to deduce stress patterns in tissues. By reducing the water potential and epidermal tension in planta, we rescued the adhesion defects in qua1, formally associating gaping and tensile stress patterns in the mutant. Using suboptimal water potential conditions, we revealed the relative contributions of shape- and growth-derived stress in prescribing maximal tension directions in aerial tissues. Consistently, the tension patterns deduced from the gaping patterns in qua1 matched the pattern of cortical microtubules, which are thought to align with maximal tension, in wild-type organs. Conversely, loss of epidermis continuity in the qua1 mutant hampered supracellular microtubule alignments, revealing that coordination through tensile stress requires cell-cell adhesion.https://elifesciences.org/articles/34460mechanical stresscell adhesionmicrotubulesplant organs |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stéphane Verger Yuchen Long Arezki Boudaoud Olivier Hamant |
spellingShingle |
Stéphane Verger Yuchen Long Arezki Boudaoud Olivier Hamant A tension-adhesion feedback loop in plant epidermis eLife mechanical stress cell adhesion microtubules plant organs |
author_facet |
Stéphane Verger Yuchen Long Arezki Boudaoud Olivier Hamant |
author_sort |
Stéphane Verger |
title |
A tension-adhesion feedback loop in plant epidermis |
title_short |
A tension-adhesion feedback loop in plant epidermis |
title_full |
A tension-adhesion feedback loop in plant epidermis |
title_fullStr |
A tension-adhesion feedback loop in plant epidermis |
title_full_unstemmed |
A tension-adhesion feedback loop in plant epidermis |
title_sort |
tension-adhesion feedback loop in plant epidermis |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2018-04-01 |
description |
Mechanical forces have emerged as coordinating signals for most cell functions. Yet, because forces are invisible, mapping tensile stress patterns in tissues remains a major challenge in all kingdoms. Here we take advantage of the adhesion defects in the Arabidopsis mutant quasimodo1 (qua1) to deduce stress patterns in tissues. By reducing the water potential and epidermal tension in planta, we rescued the adhesion defects in qua1, formally associating gaping and tensile stress patterns in the mutant. Using suboptimal water potential conditions, we revealed the relative contributions of shape- and growth-derived stress in prescribing maximal tension directions in aerial tissues. Consistently, the tension patterns deduced from the gaping patterns in qua1 matched the pattern of cortical microtubules, which are thought to align with maximal tension, in wild-type organs. Conversely, loss of epidermis continuity in the qua1 mutant hampered supracellular microtubule alignments, revealing that coordination through tensile stress requires cell-cell adhesion. |
topic |
mechanical stress cell adhesion microtubules plant organs |
url |
https://elifesciences.org/articles/34460 |
work_keys_str_mv |
AT stephaneverger atensionadhesionfeedbackloopinplantepidermis AT yuchenlong atensionadhesionfeedbackloopinplantepidermis AT arezkiboudaoud atensionadhesionfeedbackloopinplantepidermis AT olivierhamant atensionadhesionfeedbackloopinplantepidermis AT stephaneverger tensionadhesionfeedbackloopinplantepidermis AT yuchenlong tensionadhesionfeedbackloopinplantepidermis AT arezkiboudaoud tensionadhesionfeedbackloopinplantepidermis AT olivierhamant tensionadhesionfeedbackloopinplantepidermis |
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1721459847503806464 |