TY - JOUR AB - Living tissues are characterized by an intrinsically mechanochemical interplay of active physical forces and complex biochemical signaling pathways. Either feature alone can give rise to complex emergent phenomena, for example, mechanically driven glassy dynamics and rigidity transitions, or chemically driven reaction-diffusion instabilities. An important question is how to quantitatively assess the contribution of these different cues to the large-scale dynamics of biological materials. We address this in Madin-Darby canine kidney (MDCK) monolayers, considering both mechanochemical feedback between extracellular signal-regulated kinase (ERK) signaling activity and cellular density as well as a mechanically active tissue rheology via a self-propelled vertex model. We show that the relative strength of active migration forces to mechanochemical couplings controls a transition from a uniform active glass to periodic spatiotemporal waves. We parametrize the model from published experimental data sets on MDCK monolayers and use it to make new predictions on the correlation functions of cellular dynamics and the dynamics of topological defects associated with the oscillatory phase of cells. Interestingly, MDCK monolayers are best described by an intermediary parameter region in which both mechanochemical couplings and noisy active propulsion have a strong influence on the dynamics. Finally, we study how tissue rheology and ERK waves produce feedback on one another and uncover a mechanism via which tissue fluidity can be controlled by mechanochemical waves at both the local and global levels. AU - Boocock, Daniel R AU - Hirashima, Tsuyoshi AU - Hannezo, Edouard B ID - 14277 IS - 1 JF - PRX Life SN - 2835-8279 TI - Interplay between mechanochemical patterning and glassy dynamics in cellular monolayers VL - 1 ER - TY - JOUR AB - Surface curvature both emerges from, and influences the behavior of, living objects at length scales ranging from cell membranes to single cells to tissues and organs. The relevance of surface curvature in biology is supported by numerous experimental and theoretical investigations in recent years. In this review, first, a brief introduction to the key ideas of surface curvature in the context of biological systems is given and the challenges that arise when measuring surface curvature are discussed. Giving an overview of the emergence of curvature in biological systems, its significance at different length scales becomes apparent. On the other hand, summarizing current findings also shows that both single cells and entire cell sheets, tissues or organisms respond to curvature by modulating their shape and their migration behavior. Finally, the interplay between the distribution of morphogens or micro-organisms and the emergence of curvature across length scales is addressed with examples demonstrating these key mechanistic principles of morphogenesis. Overall, this review highlights that curved interfaces are not merely a passive by-product of the chemical, biological, and mechanical processes but that curvature acts also as a signal that co-determines these processes. AU - Schamberger, Barbara AU - Ziege, Ricardo AU - Anselme, Karine AU - Ben Amar, Martine AU - Bykowski, Michał AU - Castro, André P.G. AU - Cipitria, Amaia AU - Coles, Rhoslyn A. AU - Dimova, Rumiana AU - Eder, Michaela AU - Ehrig, Sebastian AU - Escudero, Luis M. AU - Evans, Myfanwy E. AU - Fernandes, Paulo R. AU - Fratzl, Peter AU - Geris, Liesbet AU - Gierlinger, Notburga AU - Hannezo, Edouard B AU - Iglič, Aleš AU - Kirkensgaard, Jacob J.K. AU - Kollmannsberger, Philip AU - Kowalewska, Łucja AU - Kurniawan, Nicholas A. AU - Papantoniou, Ioannis AU - Pieuchot, Laurent AU - Pires, Tiago H.V. AU - Renner, Lars D. AU - Sageman-Furnas, Andrew O. AU - Schröder-Turk, Gerd E. AU - Sengupta, Anupam AU - Sharma, Vikas R. AU - Tagua, Antonio AU - Tomba, Caterina AU - Trepat, Xavier AU - Waters, Sarah L. AU - Yeo, Edwina F. AU - Roschger, Andreas AU - Bidan, Cécile M. AU - Dunlop, John W.C. ID - 12710 IS - 13 JF - Advanced Materials SN - 0935-9648 TI - Curvature in biological systems: Its quantification, emergence, and implications across the scales VL - 35 ER - TY - GEN AB - The zip file includes source data used in the manuscript "CCR7 acts as both a sensor and a sink for CCL19 to coordinate collective leukocyte migration", as well as a representative Jupyter notebook to reproduce the main figures. Please see the preprint on bioRxiv and the DOI link there to access the final published version. Note the title change between the preprint and the published manuscript. A sample script for particle-based simulations of collective chemotaxis by self-generated gradients is also included (see Self-generated_chemotaxis_sample_script.ipynb) to generate exemplary cell trajectories. A detailed description of the simulation setup is provided in the supplementary information of the manuscipt. AU - Ucar, Mehmet C ID - 14279 TI - Source data for the manuscript "CCR7 acts as both a sensor and a sink for CCL19 to coordinate collective leukocyte migration" ER - TY - JOUR AB - As developing tissues grow in size and undergo morphogenetic changes, their material properties may be altered. Such changes result from tension dynamics at cell contacts or cellular jamming. Yet, in many cases, the cellular mechanisms controlling the physical state of growing tissues are unclear. We found that at early developmental stages, the epithelium in the developing mouse spinal cord maintains both high junctional tension and high fluidity. This is achieved via a mechanism in which interkinetic nuclear movements generate cell area dynamics that drive extensive cell rearrangements. Over time, the cell proliferation rate declines, effectively solidifying the tissue. Thus, unlike well-studied jamming transitions, the solidification uncovered here resembles a glass transition that depends on the dynamical stresses generated by proliferation and differentiation. Our finding that the fluidity of developing epithelia is linked to interkinetic nuclear movements and the dynamics of growth is likely to be relevant to multiple developing tissues. AU - Bocanegra, Laura AU - Singh, Amrita AU - Hannezo, Edouard B AU - Zagórski, Marcin P AU - Kicheva, Anna ID - 12837 JF - Nature Physics SN - 1745-2473 TI - Cell cycle dynamics control fluidity of the developing mouse neuroepithelium VL - 19 ER - TY - JOUR AB - To meet the physiological demands of the body, organs need to establish a functional tissue architecture and adequate size as the embryo develops to adulthood. In the liver, uni- and bipotent progenitor differentiation into hepatocytes and biliary epithelial cells (BECs), and their relative proportions, comprise the functional architecture. Yet, the contribution of individual liver progenitors at the organ level to both fates, and their specific proportion, is unresolved. Combining mathematical modelling with organ-wide, multispectral FRaeppli-NLS lineage tracing in zebrafish, we demonstrate that a precise BEC-to-hepatocyte ratio is established (i) fast, (ii) solely by heterogeneous lineage decisions from uni- and bipotent progenitors, and (iii) independent of subsequent cell type–specific proliferation. Extending lineage tracing to adulthood determined that embryonic cells undergo spatially heterogeneous three-dimensional growth associated with distinct environments. Strikingly, giant clusters comprising almost half a ventral lobe suggest lobe-specific dominant-like growth behaviours. We show substantial hepatocyte polyploidy in juveniles representing another hallmark of postembryonic liver growth. Our findings uncover heterogeneous progenitor contributions to tissue architecture-defining cell type proportions and postembryonic organ growth as key mechanisms forming the adult liver. AU - Unterweger, Iris A. AU - Klepstad, Julie AU - Hannezo, Edouard B AU - Lundegaard, Pia R. AU - Trusina, Ala AU - Ober, Elke A. ID - 14426 IS - 10 JF - PLoS Biology TI - Lineage tracing identifies heterogeneous hepatoblast contribution to cell lineages and postembryonic organ growth dynamics VL - 21 ER -