4.8 Article

Adhesion-mediated heterogeneous actin organization governs apoptotic cell extrusion

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41467-020-20563-9

Keywords

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Funding

  1. Mechanobiology Institute, USPC-NUS Grant
  2. Agence Nationale de la Recherche (ANR) [ANR-17- CE13-0013, ANR-17-CE13-0022, ANR-17-CE13-0012, ANR-11-LABX-0071]
  3. Universite de Paris IdEx [ANR-18-IDEX-0001]
  4. Ligue Contre le Cancer
  5. NUS Graduate School of Integrative Sciences & Engineering (NGS)
  6. Agence Nationale de la Recherche (ANR) [ANR-17-CE13-0022, ANR-17-CE13-0012] Funding Source: Agence Nationale de la Recherche (ANR)

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The study reveals that during cell extrusion, the actin network in neighboring cells is reorganized to include lamellipodia protrusions and discontinuous actomyosin cables. The early presence of basal lamellipodia protrusion plays a role in both basal sealing and orienting the actomyosin purse-string, with the coexistence of these mechanisms influenced by cell-cell and cell-substrate adhesions. A theoretical model explains that the integration of these cellular components results in a more efficient extrusion process.
Apoptotic extrusion is crucial in maintaining epithelial homeostasis. Current literature supports that epithelia respond to extrusion by forming a supracellular actomyosin purse-string in the neighbors. However, whether other actin structures could contribute to extrusion and how forces generated by these structures can be integrated are unknown. Here, we found that during extrusion, a heterogeneous actin network composed of lamellipodia protrusions and discontinuous actomyosin cables, was reorganized in the neighboring cells. The early presence of basal lamellipodia protrusion participated in both basal sealing of the extrusion site and orienting the actomyosin purse-string. The co-existence of these two mechanisms is determined by the interplay between the cell-cell and cell-substrate adhesions. A theoretical model integrates these cellular mechanosensitive components to explain why a dual-mode mechanism, which combines lamellipodia protrusion and purse-string contractility, leads to more efficient extrusion than a single-mode mechanism. In this work, we provide mechanistic insight into extrusion, an essential epithelial homeostasis process. Cell extrusion regulates monolayer cell density and is critical in maintaining epithelia integrity, which has implications in homeostasis, development, and cancer progression. Here the authors describe how monolayer integrate mechanical signals from tissue mechanics, cell-cell adhesion, cell-substrate adhesion and cytoskeleton coordinate cell extrusion.

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