Detail of Fig7a_CoverWith025mMGenipin



Project
SSBD:Repository
Title
Time-lapse images of NHBE cells on a dish covered by matrigel with 0.25 mM genipin
Description
Time-lapse images of NHBE cells on a dish covered by matrigel. The matrigel contained 0.25 mM genipin to modify the stiffness or viscosity of the matrigel. The data of 9 fields of view are included
Release, Updated
2025-12-03
License
CC BY 4.0
Kind
Image data
File Formats
.tif
Data size
1.6 GB

Organism
Homo sapiens ( NCBI:txid9606 )
Strain(s)
-
Cell Line
NHBE cell

Datatype
-
Molecular Function (MF)
Biological Process (BP)
epithelial cell migration cell-matrix recognition
Cellular Component (CC)
cell-substrate junction
Biological Imaging Method
phase contrast microscopy ( Fbbi:00000247 )
X scale
5.66 micrometer
Y scale
5.66 micrometer
Z scale
-
T scale
5 minutes

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

Summary of Methods
Hagiwara M, Maruyama H, Akiyama M, Koh I, Arai F. Weakening of resistance force by cell-ECM interactions regulate cell migration directionality and pattern formation. Commun Biol . 2021 Jun 28;4(1):808.
Related paper(s)

Masaya Hagiwara, Hisataka Maruyama, Masakazu Akiyama, Isabel Koh, Fumihito Arai (2021) Weakening of resistance force by cell-ECM interactions regulate cell migration directionality and pattern formation., Communications biology, Volume 4, Number 1, pp. 808

Published in 2021 Jun 28 (Electronic publication in June 28, 2021, midnight )

(Abstract) Collective migration of epithelial cells is a fundamental process in multicellular pattern formation. As they expand their territory, cells are exposed to various physical forces generated by cell-cell interactions and the surrounding microenvironment. While the physical stress applied by neighbouring cells has been well studied, little is known about how the niches that surround cells are spatio-temporally remodelled to regulate collective cell migration and pattern formation. Here, we analysed how the spatio-temporally remodelled extracellular matrix (ECM) alters the resistance force exerted on cells so that the cells can expand their territory. Multiple microfabrication techniques, optical tweezers, as well as mathematical models were employed to prove the simultaneous construction and breakage of ECM during cellular movement, and to show that this modification of the surrounding environment can guide cellular movement. Furthermore, by artificially remodelling the microenvironment, we showed that the directionality of collective cell migration, as well as the three-dimensional branch pattern formation of lung epithelial cells, can be controlled. Our results thus confirm that active remodelling of cellular microenvironment modulates the physical forces exerted on cells by the ECM, which contributes to the directionality of collective cell migration and consequently, pattern formation.
(MeSH Terms)

Contact
Masaya Hagiwara , RIKEN , Cluster for Pioneering Research , Cluster for Pioneering Research
Contributors

OMERO Dataset
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OMERO Project
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Source