Jing-hai Gong

Form-finding model shows how cytoskeleton network stiffness is realized.

In eukaryotic cells the actin-cytoskeletal network provides stiffness and the driving force that contributes to changes in cell shape and cell motility, but the elastic behavior of this network is not well understood. In this paper a two dimensional form-finding model is proposed to investigate the elasticity of the actin filament network. Utilizing an initially random array of actin filaments and actin-cross-linking proteins the form-finding model iterates until the random array is brought into a stable equilibrium configuration. With some care given to actin filament density and length, distance between host sites for cross-linkers, and overall domain size the resulting configurations from the form-finding model are found to be topologically similar to cytoskeletal networks in real cells. The resulting network may then be mechanically exercised to explore how the actin filaments deform and align under load and the sensitivity of the network’s stiffness to actin filament density, length, etc. Results of the model are consistent with the experimental literature, e.g. actin filaments tend to re-orient in the direction of stretching; and the filament relative density, filament length, and actin-cross-linking protein’s relative density, control the actin-network stiffness. The model provides a ready means of extension to more complicated domains and a three-dimensional form-finding model is under development as well as models studying the formation of actin bundles.

Affine and non-affine deformations quantified in cytoskeletal networks through three-dimensional form-finding model

Actin filaments and cross-linkers are main components of cytoskeletal networks in eukaryotic cells, and they support bending moments and axial forces respectively. A three-dimensional form-finding model is proposed in this work to investigate affine and non-affine deformations in cytoskeletal networks. In recent studies, modeling of cytoskeletal networks turns out to be a key piece in the cell mechanics puzzle. We used form-finding analysis to compute and analyze cytoskeletal models. A three-dimensional model is much more flexible and contains more elements than a two-dimensional model, and non-linear finite element analysis is difficult to converge. Thus, vector form intrinsic finite element analysis is employed here for valid results. The three-dimensional model reveals new behaviors beyond earlier two-dimensional models and better aligns with available data. Relative density of actin filaments and height of the form-finding model both play important roles in determining cytoskeletal stiffness, positively and negatively, respectively. Real cytoskeletal networks are quite mixed in terms of affine and non-affine deformations, which are quantified by internal strain energy in actin filaments and cross-linkers. Results are also influenced by actin filament relative density and height of the model. The three-dimensional form-finding model does provide much more room for intensive studies on cytoskeletal networks. In our future study, microtubules, fluidics, viscoelastic-plastic cross-linkers and even the whole cell model may be taken into account gradually to improve the cytoskeletal form-finding model.