Co-design of an in-line holographic microscope with enhanced axial resolution: selective filtering digital holography

International audienceCommon-path digital in-line holography is considered as a valuable 3D diagnostic techniques for a wide range of applications. This configuration is cost effective and relatively immune to variation in the experimental environment. Nevertheless, due to its common-path geometry, the signal to noise-ratio of the acquired hologram is weak as most of the detector (i.e. CCD/CMOS sensor) dynamics is occupied by the reference field signal, whose energy is orders of magnitude higher than the field scattered by the imaged object. As it is intrinsically impossible to modify the ratio of energy of reference to the object field, we propose a co-design approach (Optics/Data Processing) to tackle this issue. The reference to object field ratio is adjusted by adding a 4-f device to a conventional in-line holographic setup , making it possible to reduce the weight of the reference field while keeping the object field almost constant. Theoretical analysis of the Cràmer-Rao lower bounds of the corresponding imaging model illustrate the advantages of this approach. These lower bounds can be asymptotically reached using a parametric inverse problems reconstruction. This implementation results in a 60 % gain in axial localization accuracy (for of 100 µm diameter spherical objects) compared to a classical in-line holography setup

Exploring the bronzing effect at the surface of ink layers (Orale)

International audienceWe i nvestigate t he optical phenomenon responsible f or t he c olored shine that s ometimes a ppears at the surface of ink layers i n t he s pecular direction, o ften ca lled bronzing or gloss di fferential. I t seems to co me from the w avelength-dependent refractive i ndex of t he i nk, which i nduces a wavelength-dependent reflectance of t he i nk-air interface. Our experiments o n c yan and magenta i nkjet i nks confirm this t heory. C omplex refractive i ndices ca n b e ob tained from measurements of t he s pectral reflectance a nd transmittance of a t ransparency film coated with t he i nk. We pr opose a correction o f t he cl assical C lapper-Yule model in order to in clude th e c olored gloss in t he pr ediction of th e s pectral reflectance of an inked paper. We also explored effects of scattering by the micrometric or nanometric roughness of the ink surface. The micrometric roughness, easy to model with a geometrical optics model, can predict the spreading of the colored gloss ov er a l arge cone. E lectromagnetic models a ccounting for t he e ffect of t he na nometric roughness of t he surface also predict the attenuation of short wavelengths observed under collimated illumination

Chemical characterization and in vitro toxicity on human bronchial epithelial cells BEAS-2B of PM2.5_{2.5} from an urban site under industrial emission influence

Particulate Matter (PM) is one of the most relevant environment-related health issues all over the world. In 2013, the International Agency for Research on Cancer (IARC) has classified air pollution and PM as a carcinogen for humans [1]. However, the mechanisms involved in the toxicity of these particles remains poorly understood, mainly because PM are uniquely complex owing to their physicochemical characteristics. In this study, fine particles were collected in the city center of Dunkirk, northern France using a 5 stages high volume cascade impactor (Staplex® 235, 68m3/h) and a Digitel DA80 high volume sampler (30m3/h).Samples were extensively characterized for their physico-chemical properties, including trace metals, water-soluble ions and organic species. Normal human bronchial epithelial cells (BEAS-2B) were used as cell model for toxicological analysis. Cytotoxicity, PAHs-metabolizing enzymes gene expression and genotoxic alterations were evaluated after 24, 48 or 72 h of exposure considering increasing concentrations of PM$_{2.5-0.3}$, organic extracts (OE) and water-soluble fraction (WF) of PM$_{2.5-0.3}$ and PM$_{2.5}$. Several sources such as road traffic, industrial activities mainly related to steelmaking, marine emissions including sea-salts and shipping, as well as soil resuspension were found to contribute to the PM$_{2.5}$ composition. Cytotoxicity assessment results showed time and dose dependent responses, with effects mainly related to PAH compounds in PM$_{2.5}$ OE in which their content were 12 times higher than in PM$_{2.5-0.3}$ one [2]. Differences in the induction of CYP1A1, CYP1B1 and NQO1 genes expression involved in the metabolic activation of organic compounds, as well as genotoxic effects (oxidative DNA adducts, H2A.X phosphorylation) were also evidenced after cells exposure to OE and PM$_{2.5-0.3}$ [3]. These results confirm the major effect of organic compounds on toxic effects, but also the potential contribution of the inorganic fraction of the PM which maintains longer the effects in exposed cells

New genetic loci link adipose and insulin biology to body fat distribution.

Body fat distribution is a heritable trait and a well-established predictor of adverse metabolic outcomes, independent of overall adiposity. To increase our understanding of the genetic basis of body fat distribution and its molecular links to cardiometabolic traits, here we conduct genome-wide association meta-analyses of traits related to waist and hip circumferences in up to 224,459 individuals. We identify 49 loci (33 new) associated with waist-to-hip ratio adjusted for body mass index (BMI), and an additional 19 loci newly associated with related waist and hip circumference measures (P < 5 × 10(-8)). In total, 20 of the 49 waist-to-hip ratio adjusted for BMI loci show significant sexual dimorphism, 19 of which display a stronger effect in women. The identified loci were enriched for genes expressed in adipose tissue and for putative regulatory elements in adipocytes. Pathway analyses implicated adipogenesis, angiogenesis, transcriptional regulation and insulin resistance as processes affecting fat distribution, providing insight into potential pathophysiological mechanisms

Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk.

Glatiramer acetate is used therapeutically in multiple sclerosis but also known for adverse effects including elevated coronary artery disease (CAD) risk. The mechanisms underlying the cardiovascular side effects of the medication are unclear. Here, we made use of the chromosomal variation in the genes that are known to be affected by glatiramer treatment. Focusing on genes and gene products reported by drug-gene interaction database to interact with glatiramer acetate we explored a large meta-analysis on CAD genome-wide association studies aiming firstly, to investigate whether variants in these genes also affect cardiovascular risk and secondly, to identify new CAD risk genes. We traced association signals in a 200-kb region around genomic positions of genes interacting with glatiramer in up to 60 801 CAD cases and 123 504 controls. We validated the identified association in additional 21 934 CAD cases and 76 087 controls. We identified three new CAD risk alleles within the TGFB1 region on chromosome 19 that independently affect CAD risk. The lead SNP rs12459996 was genome-wide significantly associated with CAD in the extended meta-analysis (odds ratio 1.09, p = 1.58×10-12). The other two SNPs at the locus were not in linkage disequilibrium with the lead SNP and by a conditional analysis showed p-values of 4.05 × 10-10 and 2.21 × 10-6. Thus, studying genes reported to interact with glatiramer acetate we identified genetic variants that concordantly with the drug increase the risk of CAD. Of these, TGFB1 displayed signal for association. Indeed, the gene has been associated with CAD previously in both in vivo and in vitro studies. Here we establish genome-wide significant association with CAD in large human samples.This work was supported by grants from the Fondation Leducq (CADgenomics: Understanding CAD Genes, 12CVD02), the German Federal Ministry of Education and Research (BMBF) within the framework of the e:Med research and funding concept (e:AtheroSysMed, grant 01ZX1313A-2014 and SysInflame, grant 01ZX1306A), and the European Union Seventh Framework Programme FP7/2007-2013 under grant agreement no HEALTH-F2-2013-601456 (CVgenes-at-target). Further grants were received from the DFG as part of the Sonderforschungsbereich CRC 1123 (B2). T.K. was supported by a DZHK Rotation Grant. I.B. was supported by the Deutsche Forschungsgemeinschaft (DFG) cluster of excellence ‘Inflammation at Interfaces’. F.W.A. is supported by a Dekker scholarship-Junior Staff Member 2014T001 -- Netherlands Heart Foundation and UCL Hospitals NIHR Biomedical Research Centre. This work was supported by the German Research Foundation (DFG) and the Technical University of Munich within the funding programme Open Access Publishing

Changing the color of textiles with realistic visual rendering

International audienceFast and easy preview of a fabric without having to produce samples would be very profitable for textile designers, but remains a technological challenge. As a first step towards this objective, we study the possibility of making images of a real sample, and changing virtually the colors of its yarns while preserving the shine and shadow texture. We consider two types of fabrics: Jacquard weave fabrics made of polyester warp and weft yarns of different colors, and satin ribbons made of polyester and metallic yarns. For the Jacquard fabric, we make a color picture with a scanner on a sample in which the yarns have contrasted colors, threshold this image in order to distinguish the pixels corresponding to each yarn, and accordingly modify their hue and chroma values. This method is simple to operate but do not enable to simulate the angle-dependent shine. A second method, tested on the satin ribbon made of black polyester and achromatic metallic yarns, is based on polarized imaging. We analyze the polarization state of the reflected light which is different for dielectric and metallic materials illuminated by polarized light. We then add a fixed color value to the pixels representing the polyester yarns and modify the hue and chroma of the pixels representing the metallic yarns. This was performed for many incident angles of light, in order to render the twinkling effect displayed by these ribbons. We could verify through a few samples that the simulated previews reproduce real pictures with visually acceptable accuracy

Very short period grating printing combining UV interferential exposure and mechanical strain

International audienc

Very short period grating printing combining UV interferential exposure and mechanical strain

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