Micro-Nano : des comportements différents, des procédés à adapter

6 pagesL'arrivée de nanomatériaux parmi les différents matériaux utilisés en pyrotechnie pose de nombreux problèmes de mise en œuvre. En effet, leurs propriétés texturales particulières ne permettent pas de les utiliser comme des matériaux classiques. Il est impératif d'adapter les procédés de mise en œuvre habituels. Pour obtenir l'adéquation de ces nouveaux matériaux et de nos procédés, des études spécifiques du comportement des nanomatériaux au cours des procédés de mise en œuvre par coulée ont été réalisés. L'observation des écarts de comportement des nanomatériaux par rapport aux "micro-matériaux" pour une même nature chimique et des conditions identiques de mise en œuvre permet d'établir des lois de comportement spécifiques, fonction de la taille des particules manipulées. Les mentalités, comme les procédés, doivent évoluer et prendre en compte l'élévation de surface spécifique qu'offre le passage à l'échelle nanométrique. Ainsi un chargement moindre en nanomatériaux ne sera pas forcement synonyme de lacunes sur les caractéristiques du produit fini (propriétés mécaniques ou pyrotechniques). Deux questions peuvent alors se poser : faut-il adapter les formulations aux procédés, en prenant en compte les caractéristiques des matières premières ou bien adapter des procédés devant supporter des taux de chargement élevés en nanomatériaux ? Le manque de connaissance et le recul sur le comportement des nanomatériaux sont un frein à leur intégration dans des composés pyrotechniques mais les propriétés exhibées laissent présagées d'un grand intérêt en vue de l'optimisation des propriétés des composés fabriqués

Mary Anning’s legacy to French vertebrate palaeontology

peer reviewedThe real nature of marine reptile fossils found in England in between the 1700s to the beginning of the 1900s remained enigmatic, until Mary Anning's incredible fossil discoveries and their subsequent study by eminent English and French scientists. In 1820, Georges Cuvier acquired several ichthyosaur specimens found by Mary Anning, now kept or displayed in the Palaeontology Gallery of the MNHN in Paris. Four years later, Cuvier obtained a plesiosaur specimen from Mary Anning, only the second ever discovered. Cuvier was fascinated by these fossils and their study allowed him to apply his comparative anatomical method and to support his catastrophist theory. We re-examined these important specimens from an historical point of view and herein describe them taxonomically for the first time since Cuvier’s works. The Paris specimens belong to two different ichthyosaur genera (Ichthyosaurus and Leptonectes) and one plesiosaur genus (Plesiosaurus)

Отражение доходов от реализации товаров в бухгалтерском и налоговом учете

International audienc

Un lion des cavernes (Panthera (Leo) spelaea) exploité au Dryas récent : les données du gisement du Peyrat (Saint-Rabier, Dordogne, France)

Introduction À partir du Pléistocène moyen, les lions l.s. sont régulièrement mentionnés dans les cortèges fauniques d’Europe (Dietrich 1968 ; Schütt 1969 ; Bonifay 1971 ; Clot 1980 ; Sala 1990 ; Argant 1991 ; Barycka 2008 ; Marciszak & Sefaniak 2010 …). Suite aux révisions de diverses séries paléontologiques d’Eurasie (Ballésio 1980 ; Sotnikova & Nikolskiy 2006 ; Barycka 2008 ; Marciszak & Stefaniak 2010 ; Hemmer 2011 ; Sotnikova & Foronova 2014) et aux analyses paléogénétiques (Barnett et a..

Combined Liver-Kidney Transplantation With Preformed Anti-human Leukocyte Antigen Donor-Specific Antibodies

Introduction: the impact of preformed donor-specific anti-human leukocyte antigen (HLA) antibodies (pDSAs) after combined liver-kidney transplantation (CLKT) is still uncertain. Methods: we conducted a retrospective study in 8 European high-volume transplant centers and investigated the outcome of 166 consecutive CLKTs, including 46 patients with pDSAs. Results: patient survival was lower in those with pDSAs (5-year patient survival rate of 63% and 78% with or without pDSA, respectively; P = 0.04). The presence of pDSAs with a mean fluorescence intensity (MFI) ≥ 5000 (hazard ratio 4.96; 95% confidence interval: 2.3-10.9; P < 0.001) and the presence of 3 or more pDSAs (hazard ratio 6.5; 95% confidence interval: 2.5-18.8; P = 0.05) were independently associated with death. The death-censored liver graft survival was similar in patients with or without pDSAs. Kidney graft survival was comparable in both groups. (The 1- and 5-year death-censored graft survival rates were 91.6% and 79.5%, respectively, in patients with pDSAs and 93% and 88%, respectively, in the donor-specific antibody [DSA]-negative group, P = not significant). Despite a higher rate of kidney graft rejection in patients with pDSAs (5-year kidney graft survival rate without rejection of 87% and 97% with or without pDSAs, respectively; P = 0.04), kidney function did not statistically differ between both groups at 5 years post-transplantation (estimated glomerular filtration rate 45 ± 17 vs. 57 ± 29 ml/min per 1.73 m2, respectively, in patients with and without pDSAs). Five recipients with pDSAs (11.0%) experienced an antibody-mediated kidney rejection that led to graft loss in 1 patient. Conclusion: our results suggest that CLKT with pDSAs is associated with a lower patients' survival despite good recipients', liver and kidney grafts' outcome

Full assembly of HIV-1 particles requires assistance of the membrane curvature factor IRSp53

During HIV-1 particle formation, the requisite plasma membrane curvature is thought to be solely driven by the retroviral Gag protein. Here, we reveal that the cellular I-BAR protein IRSp53 is required for the progression of HIV-1 membrane curvature to complete particle assembly. siRNA-mediated knockdown of IRSp53 gene expression induces a decrease in viral particle production and a viral bud arrest at half completion. Single-molecule localization microscopy at the cell plasma membrane shows a preferential localization of IRSp53 around HIV-1 Gag assembly sites. In addition, we observe the presence of IRSp53 in purified HIV-1 particles. Finally, HIV-1 Gag protein preferentially localizes to curved membranes induced by IRSp53 I-BAR domain on giant unilamellar vesicles. Overall, our data reveal a strong interplay between IRSp53 I-BAR and Gag at membranes during virus assembly. This highlights IRSp53 as a crucial host factor in HIV-1 membrane curvature and its requirement for full HIV-1 particle assembly.Peer reviewe

A multiparameter approach to monitor disease activity in collagen-induced arthritis

Introduction: Disease severity in collagen-induced arthritis (CIA) is commonly assessed by clinical scoring of paw swelling and histological examination of joints. Although this is an accurate approach, it is also labour-intensive and the application of less invasive and less time-consuming methods is of great interest. However, it is still unclear which of these methods represents the most discriminating measure of disease activity. Methods: We undertook a comparative analysis in which different measurements of inflammation and tissue damage in CIA were studied on an individual mouse level. We compared the current gold standard methods - clinical scoring and histological examination - with alternative methods based on scoring of X-ray or micro-computed tomography (CT) images and investigated the significance of systemically expressed proteins, involved in CIA pathogenesis, that have potential as biomarkers. Results: Linear regression analysis revealed a marked association of serum matrix metalloproteinase (MMP)-3 levels with all features of CIA including inflammation, cartilage destruction and bone erosions. This association was improved by combined detection of MMP-3 and anti-collagen IgG2a antibody concentrations. In addition, combined analysis of both X-ray and micro-CT images was found to be predictive for cartilage and bone damage. Most remarkably, validation analysis using an independent data set proved that variations in disease severity, induced by different therapies, could be accurately represented by predicted values based on the proposed parameters. Conclusions: Our analyses revealed that clinical scoring, combined with serum MMP-3, anti-collagen IgG2a measurement and scoring of X-ray and micro-CT images, yields a comprehensive insight into the different aspects of disease activity in CIA