4.8 Article

Mechanical constraints to cell-cycle progression in a pseudostratified epithelium

期刊

CURRENT BIOLOGY
卷 32, 期 9, 页码 2076-+

出版社

CELL PRESS
DOI: 10.1016/j.cub.2022.03.004

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资金

  1. Francis Crick Institute [FC001204, FC001317]
  2. Wellcome Trust Investigator award [206341/Z/17/Z]
  3. Engineering and Physical Sciences Research Council [EP/M006883/1]
  4. Royal Society
  5. Wolfson Foundation through a Royal Society Wolfson Research Merit Award [WM130048]
  6. National Science Foundation [RNMS11-07444]
  7. Imperial College-Francis Crick Institute PhD studentship
  8. Francis Crick PhD fellowship
  9. EMBO [ALTF 238-2018]
  10. Vienna Science and Technology Fund (WWTF)
  11. Vienna Research Groups for Young Investigators grant [VRG17-014]
  12. Wellcome Trust [206341/Z/17/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

This study explores the mechanisms behind cell growth termination and suggests that mechanical feedback may play a role via adherens junctions. It also proposes that nuclei may play a role in sensing mechanical stress and gravity. By developing a model, the research provides important insights into nuclear migration and mechanical effects during growth.
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.

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