Mechanical Responses of Breast Cancer Cells to Substrates of Varying Stiffness Revealed by Single-Cell Measurements.

How cancer cells respond to different mechanical environments remains elusive. Here, we investigated the tension in single focal adhesions of MDA-MB-231 (metastatic breast cancer cells) and MCF-10A (normal human breast cells) cells on substrates of varying stiffness using single-cell measurements. Tension measurements in single focal adhesions using an improved FRET-based tension sensor showed that the tension in focal adhesions of MDA-MB-231 cells increased on stiffer substrates while the tension in MCF-10A cells exhibited no apparent change against the substrate stiffness. Viscoelasticity measurements using magnetic tweezers showed that the power-law exponent of MDA-MB-231 cells decreased on stiffer substrates whereas MCF-10A cells had similar exponents throughout the whole stiffness, indicating that MDA-MB-231 cells change their viscoelasticity on stiffer substrates. Such changes in tension in focal adhesions and viscoelasticity against the substrate stiffness represent an adaptability of cancer cells in mechanical environments, which can facilitate the metastasis of cancer cells to different tissues.

Strain Rate and Thickness Dependences of Elastic Modulus of Free-Standing Polymer Nanometer Films.

Elastic moduli, E, of free-standing polystyrene (PS) single-layers and polystyrene-polydimethylsiloxane (PS-PDMS) bilayers are measured by uniaxial tensile testing at room temperature under different strain rates, γ̇, and for PS thicknesses, h, from 8 to 130 nm. As γ̇ increases, E increases initially, then approaches the bulk value, Ebulk, when γ̇ exceeds a characteristic value (≡ τ-1) that decreases with increasing h. The noted variation of E with γ̇ shows that stress relaxation occurs in the films during measurement when γ̇τ ≪ 1, while the noted variation of τ-1 with h shows that thinner films relax faster. Consequently, E decreases with decreasing h if γ̇ is small, but displays independence of h if γ̇ is large. Visually, the crossover takes place at around γ̇ = 0.0015 s-1, where at γ̇τ > 1 for all films.

Evolution of 3D nanoporosity and morphology in selectively dealloying ternary Au55Cu25Si20 metallic glass ribbon with enhanced alcohol electro-oxidation performance.

Current fabrication methods of nanoporous gold (NPG) mainly rely on dealloying Ag-Au binary crystalline precursors, typically Ag65Au35, with the "dealloying threshold" or "parting limit" above 55 at%. Here we report a simple chemical dealloying process, through selective dissolution of one element from a Au55Cu25Si20 metallic glass ribbon with low 'parting limit', and a novel peculiar three-dimensional 'cone shaped protrusion' nanoporous structure which has never been reported before. In this structure, a metastable gold silicide formed in the initial dealloying stage was decomposed into gold nanoparticles and amorphous SiOx in the later coarsening stage. Our finding provides insights into the underlying relationship between 'parting limit' and atomic level structure of metallic glass. Comprehensive discussions on the porosity evolution stages as well as the correlation between the porous 'cone shaped protrusion' development and potential energy landscape are made in this report. The fabricated 3D NPG also exhibited excellent electro-oxidation catalytic ability attributed to the high density of low-coordinated atomic sites provided by the gold particle inside of 'cone shaped protrusion'.