Wrinkling in the deflation of elastic bubbles

The protein hydrophobin HFBII self-assembles into very elastic films at the surface of water; these films wrinkle readily upon compression. We demonstrate and study this wrinkling instability in the context of non-planar interfaces by forming HFBII layers at the surface of bubbles; the interfaces are then compressed by deflating the bubble. By varying the initial concentration of the hydrophobin solutions, we are able to show that buckling occurs at a critical packing fraction of protein molecules on the surface. Independent experiments show that at this packing fraction the interface has a finite positive surface tension, and not zero surface tension as is usually assumed at buckling. We attribute this non-zero wrinkling tension to the finite elasticity of these interfaces. We develop a simple geometrical model for the evolution of the wrinkle length with further deflation, and show that wrinkles start close to the needle used for deflation and grow rapidly towards the mid-plane of the bubble. This geometrical model yields predictions for the length of wrinkles in good agreement with experiments, independently of the rheological properties of the adsorbed layer

Elastometry of deflated capsules elastic moduli from shape and wrinkle analysis

Elastic capsules, prepared from droplets or bubbles attached to a capillary (as in a pendant drop tensiometer), can be deflated by suction through the capillary. We study this deflation and show that a combined analysis of the shape and wrinkling characteristics enables us to determine the elastic properties in situ. Shape contours are analyzed and fitted using shape equations derived from nonlinear membrane-shell theory to give the elastic modulus, Poisson ratio and stress distribution of the membrane. We include wrinkles, which generically form upon deflation, within the shape analysis. Measuring the wavelength of wrinkles and using the calculated stress distribution gives the bending stiffness of the membrane. We illustrate this method on two very different capsule materials: polymerized octadecyltrichlorosilane (OTS) capsules and hydrophobin (HFBII) coated bubbles. Our results are in agreement with the available rheological data. For hydrophobin coated bubbles the method reveals an interesting nonlinear behavior consistent with the hydrophobin molecules having\ud a rigid core surrounded by a softer shell

Skin TLR7 triggering promotes accumulation of respiratory dendritic cells and natural killer cells.

The TLR7 agonist imiquimod has been used successfully as adjuvant for skin treatment of virus-associated warts and basal cell carcinoma. The effects of skin TLR7 triggering on respiratory leukocyte populations are unknown. In a placebo-controlled experimental animal study we have used multicolour flow cytometry to systematically analyze the modulation of respiratory leukocyte subsets after skin administration of imiquimod. Compared to placebo, skin administration of imiquimod significantly increased respiratory dendritic cells (DC) and natural killer cells, whereas total respiratory leukocyte, alveolar macrophages, classical CD4+ T helper and CD8+ T killer cell numbers were not or only moderately affected. DC subpopulation analyses revealed that elevation of respiratory DC was caused by an increase of respiratory monocytic DC and CD11b(hi) DC subsets. Lymphocyte subpopulation analyses indicated a marked elevation of respiratory natural killer cells and a significant reduction of B lymphocytes. Analysis of cytokine responses of respiratory leukocytes after stimulation with Klebsiella pneumonia indicated reduced IFN-γ and TNF-α expression and increased IL-10 and IL-12p70 production after 7 day low dose skin TLR7 triggering. Additionally, respiratory NK cytotoxic activity was increased after 7d skin TLR7 triggering. In contrast, lung histology and bronchoalveolar cell counts were not affected suggesting that skin TLR7 stimulation modulated respiratory leukocyte composition without inducing overt pulmonary inflammation. These data suggest the possibility to modulate respiratory leukocyte composition and respiratory cytokine responses against pathogens like Klebsiella pneumonia through skin administration of a clinically approved TLR7 ligand. Skin administration of synthetic TLR7 ligands may represent a novel, noninvasive means to modulate respiratory immunity

Stationary shapes of deformable particles moving at low Reynolds numbers

Lecture Notes of the Summer School ``Microswimmers -- From Single Particle Motion to Collective Behaviour'', organised by the DFG Priority Programme SPP 1726 (Forschungszentrum J{\"{u}}lich, 2015).Comment: Pages C7.1-16 of G. Gompper et al. (ed.), Microswimmers - From Single Particle Motion to Collective Behaviour, Lecture Notes of the DFG SPP 1726 Summer School 2015, Forschungszentrum J\"ulich GmbH, Schriften des Forschungszentrums J\"ulich, Reihe Key Technologies, Vol 110, ISBN 978-3-95806-083-

Regional climate model simulations as input for hydrological applications: evaluation of uncertainties

International audienceThe ERA15 Reanalysis (1979-1993) has been dynamically downscaled over Central Europe using 4 different regional climate models. The regional simulations were analysed with respect to 2m temperature and total precipitation, the main input parameters for hydrological applications. Model results were validated against three reference data sets (ERA15, CRU, DWD) and uncertainty ranges were derived. For mean annual 2 m temperature over Germany, the simulation bias lies between -1.1°C and +0.9°C depending on the combination of model and reference data set. The bias of mean annual precipitation varies between -31 and +108 mm/year. Differences between RCM results are of the same magnitude as differences between the reference data sets

OXIDATION RATES OF MAJOR FATTY ACIDS IN FASTING NEONATAL PIGS

Thirty-two pigs were used to compare the oxidation rates of uniformly labeled (U-14C) palmitic (16:0), stearic (18:0), oleic (18:1) and linoleic (18:2) acids in fasting neonatal pigs. The pigs were allowed to nurse the sow for 24 to 48 h following birth. Subsequently, they were removed, an indwelling catheter was surgically placed in the external iliac vein and the pigs were fasted for 12 h to attain a postabsorptive state. The 14C fatty acids were administered as a single infusion (10 / μCi) via the catheter, and recovery of the label as expired 14CO2 was determined at 45-min intervals for a 6-h period. Blood samples were taken following the infusion (15, 60, 120, 240, 360 min) to monitor activity maintained within the free fatty acid (FFA) fraction of the plasma pool. The oxidation rate of each fatty acid was corrected for the difference in dose dilution using a uniform factor based on plasma concentration of 18:1. The cumulative 6-h 14CO2 recovery rates (percentage of dose) were 19.1, 6.6, 30.1 and 13.1% for 16:0, 18:0, 18:1 and 18:2, respectively. Oleic acid was oxidized at a more (P\u3c.05) rapid rate than the other fatty acids. Palmitic acid and 18:2 were oxidized more rapidly than 18:0, although the difference between 18:0 and 18:2 was not significant. Plasma FFA pools differed with respect to the proportion of infused activity remaining at various times after administration. At 60 and 120 min postinfusion, the greatest (P\u3c.05) proportion of activity was maintained in the 18:1 pool (11.9 and 6.6%, respectively, vs 7.7 and 4.3% for 16:0, 6.9 and 3.9% for 18:2 and 3.6 and 2.2% for 18:0). Palmitic acid and 18:2 had a greater (P\u3c.05) level of activity in the plasma FFA pool at 60 min than did 18:0. This same pattern was observed through 2 h, but by 240 min postinfusion, the proportion of activity remaining in each of the plasma pools was similar. Rate of oxidation appeared to correspond with plasma concentration and proportion of activity remaining in the plasma FFA pool

OXIDATION RATES OF MAJOR FATTY ACIDS IN FASTING NEONATAL PIGS

Thirty-two pigs were used to compare the oxidation rates of uniformly labeled (U-14C) palmitic (16:0), stearic (18:0), oleic (18:1) and linoleic (18:2) acids in fasting neonatal pigs. The pigs were allowed to nurse the sow for 24 to 48 h following birth. Subsequently, they were removed, an indwelling catheter was surgically placed in the external iliac vein and the pigs were fasted for 12 h to attain a postabsorptive state. The 14C fatty acids were administered as a single infusion (10 / μCi) via the catheter, and recovery of the label as expired 14CO2 was determined at 45-min intervals for a 6-h period. Blood samples were taken following the infusion (15, 60, 120, 240, 360 min) to monitor activity maintained within the free fatty acid (FFA) fraction of the plasma pool. The oxidation rate of each fatty acid was corrected for the difference in dose dilution using a uniform factor based on plasma concentration of 18:1. The cumulative 6-h 14CO2 recovery rates (percentage of dose) were 19.1, 6.6, 30.1 and 13.1% for 16:0, 18:0, 18:1 and 18:2, respectively. Oleic acid was oxidized at a more (P\u3c.05) rapid rate than the other fatty acids. Palmitic acid and 18:2 were oxidized more rapidly than 18:0, although the difference between 18:0 and 18:2 was not significant. Plasma FFA pools differed with respect to the proportion of infused activity remaining at various times after administration. At 60 and 120 min postinfusion, the greatest (P\u3c.05) proportion of activity was maintained in the 18:1 pool (11.9 and 6.6%, respectively, vs 7.7 and 4.3% for 16:0, 6.9 and 3.9% for 18:2 and 3.6 and 2.2% for 18:0). Palmitic acid and 18:2 had a greater (P\u3c.05) level of activity in the plasma FFA pool at 60 min than did 18:0. This same pattern was observed through 2 h, but by 240 min postinfusion, the proportion of activity remaining in each of the plasma pools was similar. Rate of oxidation appeared to correspond with plasma concentration and proportion of activity remaining in the plasma FFA pool