Mechanical constraints to cell-cycle progression in a pseudostratified epithelium

As organs and tissues approach their normal size during development or regeneration, growth slows down, and cell proliferation progressively comes to a halt. Among the various processes suggested to contribute to growth termination,1–10 mechanical feedback, perhaps via adherens junctions, has been s...

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Main Authors: Degond, P. (Author), Hecht, S. (Author), Merino-Aceituno, S. (Author), Perez-Mockus, G. (Author), Recasens-Alvarez, C. (Author), Salbreux, G. (Author), Schienstock, D. (Author), Smith, M. (Author), Vincent, J.-P (Author)
Format: Article
Language:English
Published: Cell Press 2022
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Online Access:View Fulltext in Publisher
LEADER 02688nam a2200301Ia 4500
001 10.1016-j.cub.2022.03.004
008 220706s2022 CNT 000 0 und d
020 |a 09609822 (ISSN) 
245 1 0 |a Mechanical constraints to cell-cycle progression in a pseudostratified epithelium 
260 0 |b Cell Press  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1016/j.cub.2022.03.004 
520 3 |a As organs and tissues approach their normal size during development or regeneration, growth slows down, and cell proliferation progressively comes to a halt. Among the various processes suggested to contribute to growth termination,1–10 mechanical feedback, perhaps via adherens junctions, has been suggested to play a role.11–14 However, since adherens junctions are only present in a narrow plane of the subapical region, other structures are likely needed to sense mechanical stresses along the apical-basal (A-B) axis, especially in a thick pseudostratified epithelium. This could be achieved by nuclei, which have been implicated in mechanotransduction in tissue culture.15 In addition, mechanical constraints imposed by nuclear crowding and spatial confinement could affect interkinetic nuclear migration (IKNM),16 which allows G2 nuclei to reach the apical surface, where they normally undergo mitosis.17–25 To explore how mechanical constraints affect IKNM, we devised an individual-based model that treats nuclei as deformable objects constrained by the cell cortex and the presence of other nuclei. The model predicts changes in the proportion of cell-cycle phases during growth, which we validate with the cell-cycle phase reporter FUCCI (Fluorescent Ubiquitination-based Cell Cycle Indicator).26 However, this model does not preclude indefinite growth, leading us to postulate that nuclei must migrate basally to access a putative basal signal required for S phase entry. With this refinement, our updated model accounts for the observed progressive slowing down of growth and explains how pseudostratified epithelia reach a stereotypical thickness upon completion of growth. © 2022 
650 0 4 |a Drosophila 
650 0 4 |a growth deceleration 
650 0 4 |a imaginal discs 
650 0 4 |a interkinetic nuclear migration 
650 0 4 |a proliferation control 
650 0 4 |a pseudostratified epithelium 
700 1 0 |a Degond, P.  |e author 
700 1 0 |a Hecht, S.  |e author 
700 1 0 |a Merino-Aceituno, S.  |e author 
700 1 0 |a Perez-Mockus, G.  |e author 
700 1 0 |a Recasens-Alvarez, C.  |e author 
700 1 0 |a Salbreux, G.  |e author 
700 1 0 |a Schienstock, D.  |e author 
700 1 0 |a Smith, M.  |e author 
700 1 0 |a Vincent, J.-P.  |e author 
773 |t Current Biology