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Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos
Through their coordinated alignment and beating, motile cilia generate directional fluid flow and organismal movement. While the mechanisms used by multiciliated epithelial tissues to achieve this coordination have been widely studied, much less is known about regulation of monociliated tissues such...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589754/ https://www.ncbi.nlm.nih.gov/pubmed/28883641 http://dx.doi.org/10.1038/s41598-017-10822-z |
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author | Mizuno, Katsutoshi Shiba, Kogiku Yaguchi, Junko Shibata, Daisuke Yaguchi, Shunsuke Prulière, Gérard Chenevert, Janet Inaba, Kazuo |
author_facet | Mizuno, Katsutoshi Shiba, Kogiku Yaguchi, Junko Shibata, Daisuke Yaguchi, Shunsuke Prulière, Gérard Chenevert, Janet Inaba, Kazuo |
author_sort | Mizuno, Katsutoshi |
collection | PubMed |
description | Through their coordinated alignment and beating, motile cilia generate directional fluid flow and organismal movement. While the mechanisms used by multiciliated epithelial tissues to achieve this coordination have been widely studied, much less is known about regulation of monociliated tissues such as those found in the vertebrate node and swimming planktonic larvae. Here, we show that a calcium sensor protein associated with outer arm dynein, calaxin, is a critical regulator for the coordinated movements of monocilia. Knockdown of calaxin gene in sea urchin embryos results in uncoordinated ciliary beating and defective directional movement of the embryos, but no apparent abnormality in axoneme ultrastructure. Examination of the beating cycle of individual calaxin-deficient cilia revealed a marked effect on the waveform and spatial range of ciliary bending. These findings indicate that calaxin-mediated regulation of ciliary beating is responsible for proper basal body orientation and ciliary alignment in fields of monociliated cells. |
format | Online Article Text |
id | pubmed-5589754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55897542017-09-13 Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos Mizuno, Katsutoshi Shiba, Kogiku Yaguchi, Junko Shibata, Daisuke Yaguchi, Shunsuke Prulière, Gérard Chenevert, Janet Inaba, Kazuo Sci Rep Article Through their coordinated alignment and beating, motile cilia generate directional fluid flow and organismal movement. While the mechanisms used by multiciliated epithelial tissues to achieve this coordination have been widely studied, much less is known about regulation of monociliated tissues such as those found in the vertebrate node and swimming planktonic larvae. Here, we show that a calcium sensor protein associated with outer arm dynein, calaxin, is a critical regulator for the coordinated movements of monocilia. Knockdown of calaxin gene in sea urchin embryos results in uncoordinated ciliary beating and defective directional movement of the embryos, but no apparent abnormality in axoneme ultrastructure. Examination of the beating cycle of individual calaxin-deficient cilia revealed a marked effect on the waveform and spatial range of ciliary bending. These findings indicate that calaxin-mediated regulation of ciliary beating is responsible for proper basal body orientation and ciliary alignment in fields of monociliated cells. Nature Publishing Group UK 2017-09-07 /pmc/articles/PMC5589754/ /pubmed/28883641 http://dx.doi.org/10.1038/s41598-017-10822-z 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 Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative 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 Mizuno, Katsutoshi Shiba, Kogiku Yaguchi, Junko Shibata, Daisuke Yaguchi, Shunsuke Prulière, Gérard Chenevert, Janet Inaba, Kazuo Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos |
title | Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos |
title_full | Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos |
title_fullStr | Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos |
title_full_unstemmed | Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos |
title_short | Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos |
title_sort | calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589754/ https://www.ncbi.nlm.nih.gov/pubmed/28883641 http://dx.doi.org/10.1038/s41598-017-10822-z |
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