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Revealing chiral cell motility by 3D Riesz transform-differential interference contrast microscopy and computational kinematic analysis

Left–right asymmetry is a fundamental feature of body plans, but its formation mechanisms and roles in functional lateralization remain unclear. Accumulating evidence suggests that left–right asymmetry originates in the cellular chirality. However, cell chirality has not yet been quantitatively inve...

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Detalles Bibliográficos
Autores principales: Tamada, Atsushi, Igarashi, Michihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736583/
https://www.ncbi.nlm.nih.gov/pubmed/29259161
http://dx.doi.org/10.1038/s41467-017-02193-w
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author Tamada, Atsushi
Igarashi, Michihiro
author_facet Tamada, Atsushi
Igarashi, Michihiro
author_sort Tamada, Atsushi
collection PubMed
description Left–right asymmetry is a fundamental feature of body plans, but its formation mechanisms and roles in functional lateralization remain unclear. Accumulating evidence suggests that left–right asymmetry originates in the cellular chirality. However, cell chirality has not yet been quantitatively investigated, mainly due to the absence of appropriate methods. Here we combine 3D Riesz transform-differential interference contrast (RT-DIC) microscopy and computational kinematic analysis to characterize chiral cellular morphology and motility. We reveal that filopodia of neuronal growth cones exhibit 3D left-helical motion with retraction and right-screw rotation. We next apply the methods to amoeba Dictyostelium discoideum and discover right-handed clockwise cell migration on a 2D substrate and right-screw rotation of subcellular protrusions along the radial axis in a 3D substrate. Thus, RT-DIC microscopy and the computational kinematic analysis are useful and versatile tools to reveal the mechanisms of left–right asymmetry formation and the emergence of lateralized functions.
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spelling pubmed-57365832017-12-21 Revealing chiral cell motility by 3D Riesz transform-differential interference contrast microscopy and computational kinematic analysis Tamada, Atsushi Igarashi, Michihiro Nat Commun Article Left–right asymmetry is a fundamental feature of body plans, but its formation mechanisms and roles in functional lateralization remain unclear. Accumulating evidence suggests that left–right asymmetry originates in the cellular chirality. However, cell chirality has not yet been quantitatively investigated, mainly due to the absence of appropriate methods. Here we combine 3D Riesz transform-differential interference contrast (RT-DIC) microscopy and computational kinematic analysis to characterize chiral cellular morphology and motility. We reveal that filopodia of neuronal growth cones exhibit 3D left-helical motion with retraction and right-screw rotation. We next apply the methods to amoeba Dictyostelium discoideum and discover right-handed clockwise cell migration on a 2D substrate and right-screw rotation of subcellular protrusions along the radial axis in a 3D substrate. Thus, RT-DIC microscopy and the computational kinematic analysis are useful and versatile tools to reveal the mechanisms of left–right asymmetry formation and the emergence of lateralized functions. Nature Publishing Group UK 2017-12-19 /pmc/articles/PMC5736583/ /pubmed/29259161 http://dx.doi.org/10.1038/s41467-017-02193-w Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commonslicense, unless indicated otherwise in a credit line to the material. If material is not included in the article’sCreative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tamada, Atsushi
Igarashi, Michihiro
Revealing chiral cell motility by 3D Riesz transform-differential interference contrast microscopy and computational kinematic analysis
title Revealing chiral cell motility by 3D Riesz transform-differential interference contrast microscopy and computational kinematic analysis
title_full Revealing chiral cell motility by 3D Riesz transform-differential interference contrast microscopy and computational kinematic analysis
title_fullStr Revealing chiral cell motility by 3D Riesz transform-differential interference contrast microscopy and computational kinematic analysis
title_full_unstemmed Revealing chiral cell motility by 3D Riesz transform-differential interference contrast microscopy and computational kinematic analysis
title_short Revealing chiral cell motility by 3D Riesz transform-differential interference contrast microscopy and computational kinematic analysis
title_sort revealing chiral cell motility by 3d riesz transform-differential interference contrast microscopy and computational kinematic analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736583/
https://www.ncbi.nlm.nih.gov/pubmed/29259161
http://dx.doi.org/10.1038/s41467-017-02193-w
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