Cells lying on a bed of microneedles: An approach to isolate mechanical force

TLDR

Summaries: Purpose: The study introduces an approach to manipulate and measure mechanical interactions between cells and substrates using microfabricated elastomeric microneedle arrays. Also the last sentence includes purpose: "Together, these findings demonstrate a coordination of biochemical and mechanical signals to regulate cell adhesion and mechanics, and they introduce the use of arrays of mechanically isolated sensors to manipulate and measure the mechanical interactions of cells." So purpose: introduce approach to manipulate/measure mechanical interactions using microneedle arrays, and show coordination of biochemical and mechanical signals. Combine: "The authors introduce a microneedle array platform to manipulate and measure cell–substrate mechanical interactions, demonstrating how biochemical signals coordinate with mechanical forces to regulate adhesion and traction." That covers purpose.

Abstract

We describe an approach to manipulate and measure mechanical interactions between cells and their underlying substrates by using microfabricated arrays of elastomeric, microneedle-like posts. By controlling the geometry of the posts, we varied the compliance of the substrate while holding other surface properties constant. Cells attached to, spread across, and deflected multiple posts. The deflections of the posts occurred independently of neighboring posts and, therefore, directly reported the subcellular distribution of traction forces. We report two classes of force-supporting adhesions that exhibit distinct force–size relationships. Force increased with size of adhesions for adhesions larger than 1 μm 2 , whereas no such correlation existed for smaller adhesions. By controlling cell adhesion on these micromechanical sensors, we showed that cell morphology regulates the magnitude of traction force generated by cells. Cells that were prevented from spreading and flattening against the substrate did not contract in response to stimulation by serum or lysophosphatidic acid, whereas spread cells did. Contractility in the unspread cells was rescued by expression of constitutively active RhoA. Together, these findings demonstrate a coordination of biochemical and mechanical signals to regulate cell adhesion and mechanics, and they introduce the use of arrays of mechanically isolated sensors to manipulate and measure the mechanical interactions of cells.