Abstract

The coordination of cell proliferation and migration in growing tissues is crucial in development and regeneration but remains poorly understood. Here, we find that, while expanding with an edge speed independent of initial conditions, millimeter-scale epithelial monolayers exhibit internal patterns of proliferation and migration that depend not on the current but on the initial tissue size, indicating memory effects. Specifically, the core of large tissues becomes very dense, almost quiescent, and ceases cell-cycle progression. In contrast, initially-smaller tissues develop a local minimum of cell density and a tissue-spanning vortex. To explain vortex formation, we propose an active polar fluid model with a feedback between cell polarization and tissue flow. Taken together, our findings suggest that expanding epithelia decouple their internal and edge regions, which enables robust expansion dynamics despite the presence of size- and history-dependent patterns in the tissue interior.

Highlights

  • The coordination of cell proliferation and migration in growing ment (7), and boundary formation (8)

  • Our findings suggest that expanding epithelia decouple their internal and edge regions, which enables robust expansion dynamics despite the presence of sizeand history-dependent patterns in the tissue interior

  • We hypothesize that the overshoot is due to the formation is independent of the initial conditions, the tissue bulk exhibits size-dependent patterns of cell proliferation and migration, including large-scale vortices accompanied by dynamic density profiles

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Summary

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46 but different initial diameters of 1.7 mm and 3.4 mm (a 4X difference in area, with tissues hereafter referred to as either “small” or “large”), using an MDCK cell line stably expressing the 2-color FUCCI cell-cycle marker (22, 31, 34–36). Time (h) patterned the tissues by culturing cells in small and large circular silicone stencils for ∼18 hrs (6, 33), whereupon stencils were removed and tissues were allowed to freely expand for 46 h (Fig. 1A, Movie S1), while images were collected

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Relative Area
Vortex timing
Ta νs
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Findings
Large tissue
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