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arXiv · 1907.10642

Centering and symmetry breaking in confined contracting actomyosin networks

Abstract

Centering and decentering of cellular components is essential for internal organization of cells and their ability to perform basic cellular functions such as division and motility. How cells achieve proper localization of their components is still not well-understood, especially in large cells such as oocytes. Here, we study actin-based positioning mechanisms in artificial cells with persistently contracting actomyosin networks, generated by encapsulating cytoplasmic Xenopus egg extracts into cell-sized water-in-oil droplets. We observe size-dependent localization of the contraction center, with a symmetric configuration in larger cells and a polar one in smaller cells. In the symmetric state, the contraction center is actively centered, via a hydrodynamic mechanism based on Darcy friction between the contracting network and the surrounding cytoplasm. During symmetry breaking, transient attachments to the cell boundary drive the contraction center to a polar location near the droplet boundary. Our findings demonstrate a robust, yet tunable, mechanism for subcellular localization.

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BibTeXRIS

Niv Ierushalmi, Maya Malik-Garbi, Angelika Manhart, Enas Abu-Shah, Bruce L. Goode, Alex Mogilner, Kinneret Keren. 2019-07-24. Centering and symmetry breaking in confined contracting actomyosin networks. https://arxiv.org/abs/1907.10642

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