Summary of ssbd-repos-000295

SSBD:database
URL

Name
ssbd-repos-000295 (295-Katoh-CiliumDyn)
URL
DOI
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Title
Images of immotile cilia dynamics in wild-type mouse embryo or iv/iv mutant embryo
Description
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Submited Date
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Release Date
2023-07-20
Updated Date
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License
Funding information
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File formats
Data size
19.1 GB

Organism
Mus musculus
Strain
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Cell Line
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Genes
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Proteins
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GO Molecular Function (MF)
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GO Biological Process (BP)
detection of nodal flow, calcium-mediated signaling, determination of left/right symmetry
GO Cellular Component (CC)
non-motile cilium
Study Type
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Imaging Methods
Spinning disk confocal microscopy, time lapse microscopy, Spinning disk confocal microscope with custom-built optical pathway, AiryScan, immunostaining, Calcium imaging, Optical-tweezers, STED, highly inclined and laminated optical sheet (HILO) microscopy, Spinning disk confocal microscopy with deconvolution, Whole-Cell FRAP (FRAPとは異なります。本論文で初めて報告した新規顕微鏡法です)

Method Summary
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Related paper(s)

Takanobu A Katoh, Toshihiro Omori, Katsutoshi Mizuno, Xiaorei Sai, Katsura Minegishi, Yayoi Ikawa, Hiromi Nishimura, Takeshi Itabashi, Eriko Kajikawa, Sylvain Hiver, Atsuko H Iwane, Takuji Ishikawa, Yasushi Okada, Takayuki Nishizaka, Hiroshi Hamada (2023) Immotile cilia mechanically sense the direction of fluid flow for left-right determination., Science (New York, N.Y.), Volume 379, Number 6627, pp. 66-71

Published in 2023 Jan 6 (Electronic publication in Jan. 5, 2023, midnight )

(Abstract) Immotile cilia at the ventral node of mouse embryos are required for sensing leftward fluid flow that breaks left-right symmetry of the body. However, the flow-sensing mechanism has long remained elusive. In this work, we show that immotile cilia at the node undergo asymmetric deformation along the dorsoventral axis in response to the flow. Application of mechanical stimuli to immotile cilia by optical tweezers induced calcium ion transients and degradation of Dand5 messenger RNA (mRNA) in the targeted cells. The Pkd2 channel protein was preferentially localized to the dorsal side of immotile cilia, and calcium ion transients were preferentially induced by mechanical stimuli directed toward the ventral side. Our results uncover the biophysical mechanism by which immotile cilia at the node sense the direction of fluid flow.
(MeSH Terms)

Contact(s)
Takanobu A. Katoh, Toshihiro Omori, Hiroshi Hamada
Organization(s)
The University of Tokyo, Tohoku University, Tata Instituite for Foundamental Research , Graduate School of Medicine, Graduate School of Biomedical Engineering, National Center for Biological Science , Cell Biology
Image Data Contributors
Quantitative Data Contributors

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