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A Bi-Stable Reaction-Diffusion Mechanism for Size-Independent Symmetry Breaking of Mouse Embryoid Bodies

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Langegger,  M
Müller Group, Friedrich Miescher Laboratory, Max Planck Society;

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Müller,  P
Müller Group, Friedrich Miescher Laboratory, Max Planck Society;

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Citation

Marcon, L., Raspopovic, J., Langegger, M., & Müller, P. (2019). A Bi-Stable Reaction-Diffusion Mechanism for Size-Independent Symmetry Breaking of Mouse Embryoid Bodies. In European Developmental Biology Congress (EDBC 2019) (pp. 67).


Cite as: https://hdl.handle.net/21.11116/0000-000B-41A4-2
Abstract
Mouse embryoid bodies can break their initial symmetry to form a localized expression of germ layer markers that resembles the formation of the anterior-posterior axis in the embryo. Here, we analyze this self-organization in three dimensions by using lightsheet microscopy. Our data shows that the formation of the anterior-posterior axis is characterized by a moving gene expression front of mesendodermal fates that propagates from the boundary on one side of the embryoid body. By developing a three-dimensional computational model of embryoid body self-organization, we show that this spatiotemporal dynamics can be recapitulated by a bi-stable reaction-diffusion mechanism under the influence of signals coming from the boundary. To test this hypothesis we analyze anterior-posterior axis self-organization in embrioid bodies of different size and upon pharmacological inhibition of signaling pathways. In agreement with the model, our data show that the formation of the axis is size-independent and that the velocity of the front is mediated by Wnt and Nodal signaling.