4.8 Article

Caveolae promote successful abscission by controlling intercellular bridge tension during cytokinesis

Journal

SCIENCE ADVANCES
Volume 8, Issue 15, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.abm5095

Keywords

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Funding

  1. Institut Pasteur
  2. CNRS
  3. ANR MOTICAV
  4. ANR SeptScort
  5. ANR CAV-SM
  6. Fondation pour le Recherche Medicale: Recherche soutenue par la [FRM EQU202103012627]
  7. French National Research Agency through the Investments for the Futureprogram, France-BioImaging [ANR-10-INSB-04]
  8. Cell and Tissue Imaging core facility (PICT-IBiSA), member of the France-BioImaging national research infrastructure - Labex Cell(n)Scale [ANR-10-LBX-0038, ANR-10-IDEX-0001-02 PSL]
  9. Doctoral School Complexite du Vivant [ED515, 2828/2017]
  10. La Ligue Contre le Cancer
  11. Pasteur-Paris University (PPU) international PhD program
  12. Fondation ARC pour la recherche sur le cancer [DOC20180507410]
  13. Programme Labellise [PGA1-RF20170205456]
  14. CEFIPRA [6301-1]

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Caveolae play a crucial role in promoting cytokinetic abscission by buffering membrane tension and limiting contractibility at the intercellular bridge.
During cytokinesis, the intercellular bridge (ICB) connecting the daughter cells experiences pulling forces, which delay abscission by preventing the assembly of the ESCRT scission machinery. Abscission is thus triggered by tension release, but how ICB tension is controlled is unknown. Here, we report that caveolae, which are known to regulate membrane tension upon mechanical stress in interphase cells, are located at the midbody, at the abscission site, and at the ICB/cell interface in dividing cells. Functionally, the loss of caveolae delays ESCRT-III recruitment during cytokinesis and impairs abscission. This is the consequence of a twofold increase of ICB tension measured by laser ablation, associated with a local increase in myosin II activity at the ICB/cell interface. We thus propose that caveolae buffer membrane tension and limit contractibility at the ICB to promote ESCRT-III assembly and cytokinetic abscission. Together, this work reveals an unexpected connection between caveolae and the ESCRT machinery and the first role of caveolae in cell division.

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