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...

Full description

Bibliographic Details
Main Authors: Stéphane Verger, Yuchen Long, Arezki Boudaoud, Olivier Hamant
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2018-04-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/34460
id doaj-ee999ca0f4034a24b9ec3e9aeb900f14
record_format Article
spelling 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
_version_ 1721459847503806464