Cortical Constriction During Abscission Involves Helices of ESCRT-III–Dependent Filaments

Julien Guizetti(Marine Biological Laboratory), Lothar Schermelleh(Center for Integrated Protein Science Munich), Jana Mäntler(Max Planck Institute of Molecular Cell Biology and Genetics), Sandra Maar(ETH Zurich), Ina Poser(Max Planck Institute of Molecular Cell Biology and Genetics), Heinrich Leonhardt(Center for Integrated Protein Science Munich), Thomas Müller‐Reichert(Marine Biological Laboratory), Daniel W. Gerlich(Marine Biological Laboratory)
Science
February 10, 2011
Cited by 483Open Access
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Abstract

After partitioning of cytoplasmic contents by cleavage furrow ingression, animal cells remain connected by an intercellular bridge, which subsequently splits by abscission. Here, we examined intermediate stages of abscission in human cells by using live imaging, three-dimensional structured illumination microscopy, and electron tomography. We identified helices of 17-nanometer-diameter filaments, which narrowed the cortex of the intercellular bridge to a single stalk. The endosomal sorting complex required for transport (ESCRT)-III co-localized with constriction zones and was required for assembly of 17-nanometer-diameter filaments. Simultaneous spastin-mediated removal of underlying microtubules enabled full constriction at the abscission site. The identification of contractile filament helices at the intercellular bridge has broad implications for the understanding of cell division and of ESCRT-III-mediated fission of large membrane structures.


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