Detail of Movie1_AQP1_mRFP



Project
SSBD:Repository
Title
Time-lapse image of vitelline arteries in AQP1-mRFP overexpressing quail embryos at E4.
Description
Time-lapse image of vitelline arteries in AQP1-mRFP overexpressing quail embryos at E4. AQP1-overexpressing cells prospectively derived from the aortic roof were found in the bloodstream.
Release, Updated
2025-11-28
License
CC BY
Kind
Image data
File Formats
.tif
Data size
610.2 MB

Organism
Coturnix japonica ( NCBITaxon:93934 )
Strain(s)
-
Cell Line
-

Datatype
-
Molecular Function (MF)
Biological Process (BP)
hemocyte migration ( GO:0035099 )
Cellular Component (CC)
Biological Imaging Method
time lapse microscopy ( Fbbi:00000249 )
confocal microscopy ( Fbbi:00000251 )
X scale
10.4 micrometer/pixel
Y scale
10.4 micrometer/pixel
Z scale
-
T scale
6 min per time interval

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
See details in Sato Y, et. al. (2023) Development. Jun 1;150(11):dev201275.
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
Yuki Sato , Kyushu University , Graduate School of Medical Sciences
Contributors

OMERO Dataset
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OMERO Project
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Source