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Biology subjects

Condor, M.

Publications and source records attributed to Condor, M..

3 recordsLinked to original sources

Traction force reconstruction assessment on real three-dimensional matrices and cellular morphologies

Traction force microscopy (TFM) allows to estimate tractions on the surface of cells when they mechanically interact with hydrogel substrates that mimic the extracellular matrix (ECM). The field of mechanobiology has a strong interest in using TFM in 3D in vitro models. However, there are a number of challenges that hamper the accuracy of 3D TFM and that are often bypassed. In this study, the computational efficiency and accuracy of TFM, referred to traction reconstruction from synthetically generated (control) ground truth solutions, are assessed from four different perspectives: magnitude of cellular pulling force (and hence strain level achieved in the hydrogel), effect of the complexity of the cellular morphology, accuracy and computational efficiency of forward vs inverse traction recovery methods, and the effect of incorrectly selecting a constitutive model that describes the behavior of the ECM (i.e. linear/nonlinear). The main results showed: (i) traction reconstruction is more challenging for complex cell morphologies, (ii) there is no significant impact of the magnitude of cellular pulling force on the overall reconstruction accuracy, and (iii) modeling a nonlinear hydrogel with a linear constitutive model leads to non-negligible errors (up to 80% and 30% for forward and inverse methodologies, respectively) in traction reconstruction. This study expands the characterization of the accuracy and efficiency of 3D TFM, highlighting important factors to be considered in future 3D TFM in vitro applications.

cell biology↗

Dynamic traction force measurements of migrating immune cells in 3D matrices

Immune cells such as natural killer (NK) cells migrate with high speeds of several {micro}m/min through dense tissue, but the traction forces are unknown. We present a method to measure dynamic traction forces of fast migrating cells in non-linear biopolymer matrices. The method accounts for the mechanical non-linearity of the 3D tissue matrix and can be applied to time series of confocal or bright-field image stacks. The method is highly sensitive over a large range of forces and object sizes, from [~]1 nN for axon growth cones up to [~]10 {micro}N for mouse intestinal organoids. We find that NK cells display bursts of large traction forces that increase with matrix stiffness and facilitate migration through tight constrictions.

biophysics↗

Synthetic fibrous hydrogels as a platform to decipher cell-matrix mechanical interactions

The interactions between cells and their direct environment are crucial for cell fate but biochemically and mechanically highly complex, and therefore, poorly understood. Despite recent advances that exposed the impact of a range of different factors, real progress remains challenging, since appropriate controllable matrices and quantitative analysis techniques that cover a range of time and length scales are unavailable. Here, we use a synthetic fibrous hydrogel with nonlinear mechanics to mimic and tailor the bi-directional cell-matrix interactions. Using advanced microscopy-based approaches, we acquire a comprehensive picture of how cellular traction forces, fiber remodeling, matrix stiffening, matrix properties and cellular behavior interact, highlighting for instance, the importance of a fibrous architecture and nonlinear mechanics of the matrix. Complete mapping of cell-matrix interactions at the cellular length scale provides indispensable information for the rational design of biomimetic materials to recreate realistic in vitro cell environments.

biophysics↗