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Engineering slit‐like channels for studying the growth of epithelial tissues in 3D‐confined spaces
Author(s) -
Alaimo Laura,
Luciano Marine,
Mohammed Danahe,
Versaevel Marie,
Bruyère Céline,
Vercruysse Eléonore,
Gabriele Sylvain
Publication year - 2020
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.27446
Subject(s) - slit , epithelium , epithelial tissue , microbiology and biotechnology , biophysics , elongation , cell , biology , chemistry , anatomy , materials science , neuroscience , ultimate tensile strength , metallurgy , genetics
The development of epithelial lumens in ducts is essential to the functioning of various organs and in organogenesis. Ductal elongation requires the collective migration of cell cohorts in three‐dimensional (3D) confined spaces, while maintaining their epithelial integrity. Epithelial lumens generally adopt circular morphologies, however abnormalities in complex physiological environments can lead to the narrowing of glandular spaces that adopt elongated and slit‐like morphologies. Here, we describe a simple method to form epithelial tissues in microchannels of various widths (100–300 µm) with a constant height of 25 µm that mimic elongated geometries of glandular spaces. The significance of this biomimetic platform has been evidenced by studying the migration of epithelial cell sheets inside these narrow slits of varying dimensions. We show that the growth of epithelial tissues in 3D‐confined slits leads to a gradient of cell density along the slit axis and that the migration cell velocity depends on the extent of the spatial confinement. Our findings indicate that nuclear orientation is higher for leader cells and depends on the slit width, whereas YAP protein was predominantly localized in the nucleus of leader cells. This method will pave the way to studies aiming at understanding how 3D‐confined spaces, which are reminiscent of in vivo pathological conditions, can affect the growth and the homeostasis of epithelial tissues.