Fast mechanosensitive and Ca-dependent reorientation of motile cilia basal bodies in the placozoan Trichoplax.

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Auteurs principaux: Leria, Marvin, Requin, Magali, Daroueche, Moina-Mkou, Richard, Fabrice, Brouilly, Nicolas, Hill, Roman, Le Bivic, André, Pasini, Andrea, Clément, Raphaël
Format: Artículo científico
Langue:en
Publié: Current biology : CB 2026
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author Leria, Marvin
Requin, Magali
Daroueche, Moina-Mkou
Richard, Fabrice
Brouilly, Nicolas
Hill, Roman
Le Bivic, André
Pasini, Andrea
Clément, Raphaël
author_facet Leria, Marvin
Requin, Magali
Daroueche, Moina-Mkou
Richard, Fabrice
Brouilly, Nicolas
Hill, Roman
Le Bivic, André
Pasini, Andrea
Clément, Raphaël
Leria, Marvin
Requin, Magali
Daroueche, Moina-Mkou
Richard, Fabrice
Brouilly, Nicolas
Hill, Roman
Le Bivic, André
Pasini, Andrea
Clément, Raphaël
collection PubMed - marine biology
contents Fast mechanosensitive and Ca-dependent reorientation of motile cilia basal bodies in the placozoan Trichoplax. Leria, Marvin Requin, Magali Daroueche, Moina-Mkou Richard, Fabrice Brouilly, Nicolas Hill, Roman Le Bivic, André Pasini, Andrea Clément, Raphaël Animals Placozoa Cilia Calcium Basal Bodies Mechanotransduction, Cellular Locomotion Locomotion driven by ciliary beating is widespread among animals and represents one of the most ancient movement strategies. The direction of ciliary beating is largely set by the orientation of the ciliary basal bodies (BBs), itself determined by the ciliary rootlet. In most animals, BB orientation is set along global body axes. The placozoan Trichoplax challenges this view. This small flat marine animal lacks a defined body plan yet efficiently crawls on solid substrates and continuously changes shape thanks to the thousands of cilia on its lower epithelium that can swiftly change beating direction. This raises a key question: how is ciliary beating orientation coordinated and reoriented across scales in the absence of a fixed body plan? Here, we immunostain rootlets to map BB orientation across the entire Trichoplax lower epithelium. Combining this approach with animal tracking reveals that BBs are globally aligned with the instantaneous direction of animal movement and that large-scale spatial variation of BB orientation underlies body-shape changes. Strikingly, BBs can also reorient collectively in a few seconds in response to external mechanical stimuli, revealing a coupling between mechanical cues and ciliary beating direction that enables rapid negative mechanotactic responses. Treatment with pharmacological inhibitors shows that this phenomenon depends on the activity of voltage-gated calcium channels. Together, our results uncover a rapid and coordinated mechanism of BB reorientation that links subcellular organization to whole-animal behavior, providing a framework to understand how ciliary locomotion emerges in the absence of fixed body axes.
format Artículo científico
id pubmed_42167219
institution PubMed
language en
publishDate 2026
publisher Current biology : CB
record_format pubmed
spellingShingle Fast mechanosensitive and Ca-dependent reorientation of motile cilia basal bodies in the placozoan Trichoplax.
Leria, Marvin
Requin, Magali
Daroueche, Moina-Mkou
Richard, Fabrice
Brouilly, Nicolas
Hill, Roman
Le Bivic, André
Pasini, Andrea
Clément, Raphaël
Animals
Placozoa
Cilia
Calcium
Basal Bodies
Mechanotransduction, Cellular
Locomotion
Fast mechanosensitive and Ca-dependent reorientation of motile cilia basal bodies in the placozoan Trichoplax. Leria, Marvin Requin, Magali Daroueche, Moina-Mkou Richard, Fabrice Brouilly, Nicolas Hill, Roman Le Bivic, André Pasini, Andrea Clément, Raphaël Animals Placozoa Cilia Calcium Basal Bodies Mechanotransduction, Cellular Locomotion Locomotion driven by ciliary beating is widespread among animals and represents one of the most ancient movement strategies. The direction of ciliary beating is largely set by the orientation of the ciliary basal bodies (BBs), itself determined by the ciliary rootlet. In most animals, BB orientation is set along global body axes. The placozoan Trichoplax challenges this view. This small flat marine animal lacks a defined body plan yet efficiently crawls on solid substrates and continuously changes shape thanks to the thousands of cilia on its lower epithelium that can swiftly change beating direction. This raises a key question: how is ciliary beating orientation coordinated and reoriented across scales in the absence of a fixed body plan? Here, we immunostain rootlets to map BB orientation across the entire Trichoplax lower epithelium. Combining this approach with animal tracking reveals that BBs are globally aligned with the instantaneous direction of animal movement and that large-scale spatial variation of BB orientation underlies body-shape changes. Strikingly, BBs can also reorient collectively in a few seconds in response to external mechanical stimuli, revealing a coupling between mechanical cues and ciliary beating direction that enables rapid negative mechanotactic responses. Treatment with pharmacological inhibitors shows that this phenomenon depends on the activity of voltage-gated calcium channels. Together, our results uncover a rapid and coordinated mechanism of BB reorientation that links subcellular organization to whole-animal behavior, providing a framework to understand how ciliary locomotion emerges in the absence of fixed body axes.
title Fast mechanosensitive and Ca-dependent reorientation of motile cilia basal bodies in the placozoan Trichoplax.
topic Animals
Placozoa
Cilia
Calcium
Basal Bodies
Mechanotransduction, Cellular
Locomotion
url https://pubmed.ncbi.nlm.nih.gov/42167219/