Manuscript about microtubule bridges in formation of Kupffer’s vesicle, spearheaded by Hehnly lab, appears in Nature Communications.

Former postdoctoral associate Gonca Erdemci-Tandogan and Lisa Manning worked with Heidi Hehnly’s lab (SU Biology) and Jeff Amack’s lab (SUNY Upstate Cell and Developmental Biology) to understand cytokinetic bridges that occur during formation of Kupffer’s vesicle, the organ responsible for left-right symmetry breaking in zebrafish. The manuscript recently appeared in Nature Communications: https://www.nature.com/articles/s41467-020-15002-8

Manuscript on small-scale demixing in confluent biological tissues appears in Soft Matter

Our paper, “Small-scale demixing in confluent biological tissues” just appeared in Soft Matter.

Surface tension governed by differential adhesion can drive fluid particle mixtures to sort into separate regions, i.e., demix. Does the same phenomenon occur in confluent biological tissues? We begin to answer this question for epithelial monolayers with a combination of theory via a vertex model and experiments on keratinocyte monolayers. Vertex models are distinct from particle models in that the interactions between the cells are shape-based, as opposed to distance-dependent. We investigate whether a disparity in cell shape or size alone is sufficient to drive demixing in bidisperse vertex model fluid mixtures. Surprisingly, we observe that both types of bidisperse systems robustly mix on large lengthscales. On the other hand, shape disparity generates slight demixing over a few cell diameters, a phenomenon we term micro-demixing. This result can be understood by examining the differential energy barriers for neighbor exchanges (T1 transitions). Experiments with mixtures of wild-type and E-cadherin-deficient keratinocytes on a substrate are consistent with the predicted phenomenon of micro-demixing, which biology may exploit to create subtle patterning. The robustness of mixing at large scales, however, suggests that despite some differences in cell shape and size, progenitor cells can readily mix throughout a developing tissue until acquiring means of recognizing cells of different types.

https://pubs.rsc.org/en/Content/ArticleLanding/2020/SM/C9SM01084J#!divAbstract

Manuscript on non-linear response of ordered biological tissues appears in Soft Matter

Our paper, “Linear and nonlinear mechanical responses can be quite different in models for biological tissues” just appeared in Soft Matter.

The fluidity of biological tissues – whether cells can change neighbors and rearrange – is important for their function. In traditional materials, researchers have used linear response functions, such as the shear modulus, to accurately predict whether a material will behave as a fluid. Similarly, in disordered 2D vertex models for confluent biological tissues, the shear modulus becomes zero precisely when the cells can change neighbors and the tissue fluidizes, at a critical value of control parameter s0* = 3.81. However, the ordered ground states of 2D vertex models become linearly unstable at a lower value of control parameter (3.72), suggesting that there may be a decoupling between linear and nonlinear response. We demonstrate that the linear response does not correctly predict the nonlinear behavior in these systems: when the control parameter is between 3.72 and 3.81, cells cannot freely change neighbors even though the shear modulus is zero. These results highlight that the linear response of vertex models should not be expected to generically predict their rheology. We develop a simple geometric ansatz that correctly predicts the nonlinear response, which may serve as a framework for making nonlinear predictions in other vertex-like models.

https://pubs.rsc.org/en/content/articlelanding/2020/sm/c9sm01068h#!divAbstract

Manuscript on the role of cell divisions in confluent tissue fluidization appears in Soft Matter

Our paper, “Glassy dynamics in models of confluent tissue with mitosis and apoptosis” just appeared in Soft Matter.

Recent work on particle-based models of tissues has suggested that any finite rate of cell division and cell death is sufficient to fluidize an epithelial tissue. At the same time, experimental evidence has indicated the existence of glassy dynamics in some epithelial layers despite continued cell cycling. To address this discrepancy, we quantify the role of cell birth and death on glassy states in confluent tissues using simulations of an active vertex model that includes cell motility, cell division, and cell death. Our simulation data is consistent with a simple ansatz in which the rate of cell-life cycling and the rate of relaxation of the tissue in the absence of cell cycling contribute independently and additively to the overall rate of cell motion. Specifically, we find that a glass-like regime with caging behavior indicated by subdiffusive cell displacements can be achieved in systems with sufficiently low rates of cell cycling.

https://pubs.rsc.org/en/content/articlelanding/2019/sm/c9sm00916g#!divAbstract

Julia Giannini and Ethan Stanifer Awarded BioInspired Institute Poster Session Prizes

The BioInspired Institute held it’s kickoff event on October 11, featuring PI pitch talks, a brainstorming session, and a poster session for students and postdocs. At the poster session Julia and Ethan were awarded prizes for the presentation of their respective work entitled “Predicting crowd dynamics using local structure” and “Structural evolution of amorphous systems during large scale deformation.”

Read more about the BioInspired Institute here:

https://news.syr.edu/blog/2019/04/25/bioinspired-institute-brings-together-faculty-with-related-research-interests-from-across-the-university/

Manuscript with Kasza lab on BioRXiv

We have posted a manuscript on BioRXiv: Xun Wang*, Matthias Merkel*, Leo B. Sutter*, Gonca Erdemci-Tandogan, M. Lisa Manning, Karen E. Kasza. “Anisotropy links cell shapes to a solid-to-fluid transition during convergent extension”,  https://doi.org/10.1101/781492 (2019).  In this manuscript we use a combination of vertex models and experimental analysis of convergent extension in the fruit fly to understand how the fluid-solid transition is affected by anisotropic stresses.

Manuscript with Gardel lab on BioRXiv

We posted a joint manuscript between the Manning group (Sussman, Manning) and the Gardel lab (Devaney, Gardel) on BioRXiv, titled, “Cell division Rate Controls Cell Shape Remodeling in Epithelia”, https://www.biorxiv.org/content/10.1101/804294v1. We use a combination of vertex modeling and experiments to demonstrate that cell shape (and not number density) governs cell movements in epithelia, and that cell divisions generate the dominant active stress fluctuations that cause cell movements.

Elizabeth Lawson-Keister Attends the Boulder School.

Liz was accepted to study at the 2019 Boulder Summer School for Theoretical Biophysics. The program provides education for advanced graduate students and postdoctoral fellows working in condensed matter physics, materials science and related fields. Liz will be presenting her preliminary work on cellular tissues and morphogen gradients and Dr. Manning will give lectures on topics in soft matter and biophysics.