High transcript levels of heat-shock genes are associated with shorter lifespan of Caenorhabditis elegans.

Individual lifespans of isogenic organisms, such as Caenorhabditis elegans nematodes, fruit flies, and mice, vary greatly even under identical environmental conditions. To study the molecular mechanisms responsible for such variability, we used an assay based on the measurement of post-reproductive nematode movements stimulated by a moderate electric field. This assay allows for the separation of individual nematodes based on their speed. We show that this phenotype could be used as a biomarker for aging because it is a better predictor of lifespan than chronological age. Fast nematodes have longer lifespans, fewer protein carbonyls, higher heat-shock resistance, and higher transcript levels of the daf-16 and hsf-1 genes, which code for the stress response transcription factors, than slow nematodes. High transcript levels of the genes coding for heat-shock proteins observed in slow nematodes correlate with lower heat-shock resistance, more protein carbonyls, and shorter lifespan. Taken together, our data suggests that shorter lifespan results from early-life damage accumulation that causes subsequent faster age-related deterioration.

An elasto-hydrodynamical model of friction for the locomotion of Caenorhabditis elegans.

Caenorhabditis elegans (C. elegans) is one of the most studied organisms by biologists. Composed of around one thousand cells, easy to culture and to modify genetically, it is a good model system to address fundamental physiological questions and in particular to investigate neuromuscular processes. Many C. elegans mutants can be distinguished by their locomotion phenotype and it then important to understand the biomechanics of their locomotion and in particular the mechanics of their undulating crawling motion on agar aqueous gels where they are commonly grown and observed. In this article, we present a mechanical model of the friction of the worms on their substrate where we have included capillarity (which pins the worm of the gel), the hydrodynamics of the lubrication film (between worm and gel) and the substrate/body elasticity. We determine the ratio of the transverse to longitudinal friction coefficients of the worm body on the culture gel as a function of a control parameter which describes the relative role of the deformation of the gel and the viscous dissipation in the lubrication film. Experimentally this ratio is - for soft gels - larger than the maximal value predicted by our model (this maximum is equal to 2, the value for an infinite cylinder in bulk liquid) and we propose to include the plasticity of the gel (i.e. the dissipation of the deformation of the gel) for a better description of the worm/gel interaction.

Traction forces exerted by epithelial cell sheets.

Whereas the adhesion and migration of individual cells have been well described in terms of physical forces, the mechanics of multicellular assemblies is still poorly understood. Here, we study the behavior of epithelial cells cultured on microfabricated substrates designed to measure cell-to-substrate interactions. These substrates are covered by a dense array of flexible micropillars whose deflection enables us to measure traction forces. They are obtained by lithography and soft replica molding. The pillar deflection is measured by video microscopy and images are analyzed with home-made multiple particle tracking software. First, we have characterized the temporal and spatial distributions of traction forces of cellular assemblies of various sizes. The mechanical force balance within epithelial cell sheets shows that the forces exerted by neighboring cells strongly depend on their relative position in the monolayer: the largest deformations are always localized at the edge of the islands of cells in the active areas of cell protrusions. The average traction stress rapidly decreases from its maximum value at the edge but remains much larger than the inherent noise due to the force resolution of our pillar tracking software, indicating an important mechanical activity inside epithelial cell islands. Moreover, these traction forces vary linearly with the rigidity of the substrate over about two decades, suggesting that cells exert a given amount of deformation rather than a force. Finally, we engineer micropatterned substrates supporting pillars with anisotropic stiffness. On such substrates cellular growth is aligned with respect to the stiffest direction in correlation with the magnitude of the applied traction forces.

Adsorption of polyampholytes on charged surfaces.

We have studied the adsorption of neutral polyampholytes on model charged surfaces that have been characterized by contact angle and streaming current measurements. The loop size distributions of adsorbed polymer chains have been obtained using atomic-force microscopy (AFM) and compared to recent theoretical predictions. We find a qualitative agreement with theory; the higher the surface charge, the smaller the number of monomers in the adsorbed layer. We propose an original scenario for the adsorption of polyampholytes on surfaces covered with both neutral long-chain and charged short-chain thiols.

Deformation and flow of a two-dimensional foam under continuous shear.

We investigate the flow properties of a 2D foam (a confined monolayer of jammed bubbles) submitted to a continuous shear in a Couette geometry. A strong localization of the flow at the moving inner wall is evidenced. Moreover, velocity fluctuations measurements reveal self-similar dynamical structures consisting of clusters of bubbles moving coherently. A stochastic model is proposed where bubbles rearrangements are activated by local stress fluctuations produced by the shearing wheel. This model gives a complete description of our observations and is also consistent with available data on granular shear bands.

Drug delivery: piercing vesicles by their adsorption onto a porous medium.

Experimental evidence is presented that supports the possibility of building a "molecular drill." By the adsorption of a vesicle onto a porous substrate (specifically, a lycopode grain), it was possible to increase the permeability of the vesicle by locally stretching its membrane. Molecules contained within the vesicle, which could not cross the membrane, were delivered to the porous substrate upon adsorption. This general process could provide another method for drug delivery and targeting.

Spreading of liquids on highly curved surfaces.

Because of surface tension, liquid films coating fibers or the insides of capillary tubes are usually unstable and break up into a periodic array of droplets. However, if these films are very thin (of thickness in the range of tens of angstroms), they can be stabilized by long-range van der Waals forces. A simple method for making such wetting films consists of slowly drawing the fiber out of a bath of liquid; the thickness of the film is then measured using a method based on gas chromatography. If these liquid films are thick, and are forced to flow, they may then not break up: the instability becomes "saturated."