Summary of ssbd-repos-000310

SSBD:database
URL

Name
ssbd-repos-000310 (310-Sato-HemocyteMigrate)
URL
DOI
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Title
Aquaporin overexpression promotes endothelial-to-hematopoietic transition.
Description
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Submited Date
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Release Date
2025-11-28
Updated Date
-
License
Funding information
-
File formats
Data size
22.7 GB

Organism
Coturnix japonica
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)
NA
GO Biological Process (BP)
hemocyte migration, embryonic hemopoiesis
GO Cellular Component (CC)
NA
Study Type
NA
Imaging Methods
confocal microscopy, time lapse microscopy

Method Summary
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Related paper(s)

Yuki Sato, Mugiho Shigematsu, Maria Shibata-Kanno, Sho Maejima, Chie Tamura, Hirotaka Sakamoto (2023) Aquaporin regulates cell rounding through vacuole formation during endothelial-to-hematopoietic transition., Development (Cambridge, England), Volume 150, Number 11

Published in 2023 Jun 1 (Electronic publication in June 5, 2023, midnight )

(Abstract) Endothelial-to-hematopoietic transition (EHT) is crucial for hematopoietic stem cell (HSC) generation. During EHT, the morphology of hemogenic endothelial cells (HECs) changes from flat and adherent to spherical hematopoietic cells, which detach from the dorsal aorta. HECs attain a rounded shape in a mitosis-independent manner before cell adhesion termination, suggesting an atypical cell-rounding mechanism. However, the direct mechanisms underlying this change in cell morphology during EHT remain unclear. Here, we show that large vacuoles were transiently formed in avian HECs, and that aquaporin 1 (AQP1) was localized in the vacuole and plasma membranes. Overexpression of AQP1 in non-HECs induced ectopic vacuole expansion, cell rounding and subsequent cell detachment from the endothelium into the bloodstream, mimicking EHT. Loss of redundant AQP functions by CRISPR/Cas9 gene editing in HECs impeded the morphological EHT. Our findings provide the first evidence to indicate that morphological segregation of hematopoietic cells from endothelial cells is regulated by water influx into vacuoles. These findings provide important insights for further exploration of the mechanisms underlying cell/tissue morphogenesis through water-adoptive cellular responses.
(MeSH Terms)

Contact(s)
Yuki Sato
Organization(s)
Kyushu University , Graduate School of Medical Sciences
Image Data Contributors
Quantitative Data Contributors

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