Directional ciliary beats across epithelia require Ccdc57-mediated coupling between axonemal orientation and basal body polarity

Motile cilia unify their axonemal orientations (AOs), or beat directions, across epithelia to drive liquid flows. This planar polarity results from cytoskeleton-driven swiveling of basal foot (BF), a basal body (BB) appendage coincident with the AO, in response to regulatory cues. How and when the BF-AO relationship is established, however, are unaddressed. Here, we show that the BF-AO coupling occurs during rotational polarizations of BBs and requires Ccdc57. Ccdc57 localizes on BBs as a rotationally-asymmetric punctum, which polarizes away from the BF in BBs having achieved the rotational polarity to probably fix the BF-AO relationship. Consistently, Ccdc57-deficient ependymal multicilia lack the BF-AO coupling and display directional beats at only single cell level. Ccdc57 <sup>-/-</sup> tracheal multicilia also fail to fully align their BFs. Furthermore, Ccdc57 <sup>-/-</sup> mice manifest severe hydrocephalus, due to impaired cerebrospinal fluid flow, and high mortality. These findings unravel mechanisms governing the planar polarity of epithelial motile cilia.

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Publication Details

Journal
Nature Communications
Published
2024-11-26
DOI
https://doi.org/10.1038/s41467-024-54766-1
Citations
5
Primary Topic
Protist diversity and phylogeny
Type
article
Field-Weighted Citation Impact
1.17

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article

Directional ciliary beats across epithelia require Ccdc57-mediated coupling between axonemal orientation and basal body polarity

Xiumin Yan, Lele Xie, L. J Li, Chuyu Fang et al.
5 citations
Nature Communications
Protist diversity and phylogeny
1.17
article

Directional ciliary beats across epithelia require Ccdc57-mediated coupling between axonemal orientation and basal body polarity

Xiumin Yan, Lele Xie, L. J Li, Chuyu Fang, Xixia Li, Shan Huang, Xinwen Pan, Xueliang Zhu, Chuan Shen
article en
5 citations

Abstract

Motile cilia unify their axonemal orientations (AOs), or beat directions, across epithelia to drive liquid flows. This planar polarity results from cytoskeleton-driven swiveling of basal foot (BF), a basal body (BB) appendage coincident with the AO, in response to regulatory cues. How and when the BF-AO relationship is established, however, are unaddressed. Here, we show that the BF-AO coupling occurs during rotational polarizations of BBs and requires Ccdc57. Ccdc57 localizes on BBs as a rotationally-asymmetric punctum, which polarizes away from the BF in BBs having achieved the rotational polarity to probably fix the BF-AO relationship. Consistently, Ccdc57-deficient ependymal multicilia lack the BF-AO coupling and display directional beats at only single cell level. Ccdc57 <sup>-/-</sup> tracheal multicilia also fail to fully align their BFs. Furthermore, Ccdc57 <sup>-/-</sup> mice manifest severe hydrocephalus, due to impaired cerebrospinal fluid flow, and high mortality. These findings unravel mechanisms governing the planar polarity of epithelial motile cilia.

Nature CommunicationsVol. 15(1)
Shanghai Jiao Tong University (CN), Chinese Academy of Sciences (CN), XinHua Hospital (CN), ShanghaiTech University (CN), Westlake University (CN), Institute of Biophysics (CN), Ministry of Education (KR), Center for Excellence in Molecular Cell Science (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Institute of Biophysics, Chinese Academy of Sciences
Zero hunger
Openalex Percentile: Top 21%
Protist diversity and phylogeny
1.17
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