Gradient Mechanical Properties Facilitate <i>Arabidopsis</i> Trichome as Mechanosensor

It has been reported that <i>Arabidopsis thaliana</i> leaf trichome can act as a mechanosensory switch, transducing mechanical stimuli into physiological signals, mainly through a buckling instability to focus external force (e.g., exerted by insects) on the base of trichome. The material and structural properties of trichomes remain largely unknown in this buckling instability. In this report, we mainly focused on material standpoint to explore the possible mechanism facilitating the buckling instability. We observed that the Young’s modulus of trichome cell wall decreased gradually from branch to the base region of trichome. Interestingly, we also found a corresponding decline of calcium concentration on the trichome cell wall. Results of finite element method (FEM) simulation suggested that such a gradient distribution of Young’s modulus significantly promotes force focusing and buckling instability on the base of trichome. It is indicated that <i>Arabidopsis</i> trichome has developed into an active mechanosensor benefiting from gradient cell wall mechanical properties

Patterning Cellular Alignment through Stretching Hydrogels with Programmable Strain Gradients

The graded mechanical properties (e.g., stiffness and stress/strain) of excellular matrix play an important role in guiding cellular alignment, as vital in tissue <i>reconstruction with proper functions</i>. Though various methods have been developed to engineer a graded mechanical environment to study its effect on cellular behaviors, most of them failed to distinguish stiffness effect from stress/strain effect during mechanical loading. Here, we construct a mechanical environment with programmable strain gradients by using a hydrogel of a linear elastic property. When seeding cells on such hydrogels, we demonstrate that the pattern of cellular alignment can be rather precisely tailored by substrate strains. The experiment is in consistency with a theoritical prediction when assuming that focal adhesions (FAs) would drive a cell to reorient to the directions where they are most stable. A fundamental theory has also been developed and is excellent in agreement with the complete temporal alignment of cells. This work not only provides important insights into the cellular response to the local mechanical microenvironment but can also be utilized to engineer patterned cellular alignment that can be critical in tissue remodeling and regenerative medicine applications