Summary of ssbd-repos-000380

SSBD:database
URL

Name
ssbd-repos-000380 (380-Wang-ActininTensionSensor)
URL
DOI
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Title
Changes of tension in smooth muscle cell after treatment with water, calyculin A, or Y27632
Description
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Submited Date
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Release Date
2024-12-14
Updated Date
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License
Funding information
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File formats
Data size
3.4 GB

Organism
Mus musculus
Strain
R26R-S2 (Accession No. CDB0055E)
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)
response to chemical, response to osmotic stress
GO Cellular Component (CC)
cytoskeleton
Study Type
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Imaging Methods
time lapse microscopy, confocal microscopy, FRET

Method Summary
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Related paper(s)

Junfeng Wang, Eijiro Maeda, Yuki Tsujimura, Takaya Abe, Hiroshi Kiyonari, Tetsuya Kitaguchi, Hideo Yokota, Takeo Matsumoto (2023) In situ FRET measurement of cellular tension using conventional confocal laser microscopy in newly established reporter mice expressing actinin tension sensor., Scientific reports, Volume 13, Number 1, pp. 22729

Published in 2023 Dec 20 (Electronic publication in Dec. 20, 2023, midnight )

(Abstract) FRET-based sensors are utilized for real-time measurements of cellular tension. However, transfection of the sensor gene shows low efficacy and is only effective for a short period. Reporter mice expressing such sensors have been developed, but sensor fluorescence has not been measured successfully using conventional confocal microscopy. Therefore, methods for spatiotemporal measurement of cellular tension in vivo or ex vivo are still limited. We established a reporter mouse line expressing FRET-based actinin tension sensors consisting of EGFP as the donor and mCherry as the acceptor and whose FRET ratio change is observable with confocal microscopy. Tension-induced changes in FRET signals were monitored in the aorta and tail tendon fascicles, as well as aortic smooth muscle cells isolated from these mice. The pattern of FRET changes was distinctive, depending on tissue type. Indeed, aortic smooth muscle cells exhibit different sensitivity to macroscopic tensile strain in situ and in an isolated state. This mouse strain will enable novel types of biomechanical investigations of cell functions in important physiological events.
(MeSH Terms)

Contact(s)
Takeo Matsumoto
Organization(s)
Nagoya University , Biomechanics Laboratory, Department of Mechanical Systems Engineering, Graduate School of Engineering , Biomechanics Laboratory, Department of Mechanical Systems Engineering, Graduate School of Engineering
Image Data Contributors
Quantitative Data Contributors

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