652 research outputs found

    The 2mrad horizontal crossing angle IR layout for a TeV ILC

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    The current status of the 2mrad crossing angle layout for the ILC is reviewed. The scheme developed in the UK and France is described and the performance discussed for a TeV machine. Secondly, the scheme developed at SLAC and BNL is then studied and modified for a TeV machine. We find that both schemes can handle the higher energy beam with modifications, and share many common features.Comment: The proceedings of the 2005 International Linear Collider Workshop, March 2005. 4 pages, 5 figure

    UHE tau neutrino flux regeneration while skimming the Earth

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    The detection of Earth-skimming tau neutrinos has turned into a very promising strategy for the observation of ultra-high energy cosmic neutrinos. The sensitivity of this channel crucially depends on the parameters of the propagation of the tau neutrinos through the terrestrial crust, which governs the flux of emerging tau leptons that can be detected. One of the characteristics of this propagation is the possibility of regeneration through multiple νττ\nu_\tau \leftrightarrow \tau conversions, which are often neglected in the standard picture. In this paper, we solve the transport equations governing the ντ\nu_\tau propagation and compare the flux of emerging tau leptons obtained allowing regeneration or not. We discuss the validity of the approximation of neglecting the ντ\nu_\tau regeneration using different scenarios for the neutrino-nucleon cross-sections and the tau energy losses.Comment: 8 pages, 8 figure

    Colchicine therapy in acute coronary syndrome patients acts on caspase-1 to suppress NLRP3 inflammasome monocyte activation

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    Inflammasome activation, with subsequent release of pro-inflammatory cytokines interleukin-1β (IL-1β) and IL-18, has recently been implicated in atherosclerosis-associated inflammation. This study aims to assess in acute coronary syndrome (ACS) patients (1) inflammasome activation in circulating monocytes and (2) whether short-term oral colchicine, a recognized anti-inflammatory agent that has been shown to be cardio-protective in clinical studies, might acutely suppress inflammasome-dependent inflammation. ACS patients (n=21) were randomized to oral colchicine (1 mg followed by 0.5 mg 1 h later) or no treatment, and compared with untreated healthy controls (n=9). Peripheral venous blood was sampled pre- (day 1) and 24 h post- (day 2) treatment. Monocytes were cultured and stimulated with ATP. Analysis of key inflammasome markers was performed by ELISA. IL-1β secretion increased by 580.4% (P<0.01) in ACS patients compared with controls but only with ATP stimulation. Untreated ACS patients secreted significantly higher levels of IL-18 compared with healthy controls independent of ATP stimulation (P<0.05). Colchicine treatment in ACS patients markedly reduced intracellular and secreted levels of IL-1β compared with pre-treatment levels (P<0.05 for both), as well as significantly reducing pro-caspase-1 mRNA levels by 57.7% and secreted caspase-1 protein levels by 30.2% compared with untreated patients (P<0.05 for both). Monocytes from ACS patients are ‘primed’ to secrete inflammasome-related cytokines and short-term colchicine acutely and markedly suppresses monocyte caspase-1 activity, thereby reducing monocyte secretion of IL-1β

    Tau energy losses at ultra-high energy: continuous versus stochastic treatment

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    We study the energy losses of the tau lepton in matter through electromagnetic processes at ultra-high energy (UHE). We use both a stochastic and a continuous framework to treat these interactions and compare the flux of tau leptons propagated after some amount of matter. We discuss the accuracy of the approximation of continuous energy losses by studying the propagation in standard rock of taus with both mono-energetic and power law injection spectra.Comment: 7 pages, 8 figure

    Model for the on-site matrix elements of the tight-binding hamiltonian of a strained crystal: Application to silicon, germanium and their alloys

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    We discuss a model for the on-site matrix elements of the sp3d5s* tight-binding hamiltonian of a strained diamond or zinc-blende crystal or nanostructure. This model features on-site, off-diagonal couplings between the s, p and d orbitals, and is able to reproduce the effects of arbitrary strains on the band energies and effective masses in the full Brillouin zone. It introduces only a few additional parameters and is free from any ambiguities that might arise from the definition of the macroscopic strains as a function of the atomic positions. We apply this model to silicon, germanium and their alloys as an illustration. In particular, we make a detailed comparison of tight-binding and ab initio data on strained Si, Ge and SiGe.Comment: Submitted to Phys. Rev.

    Nine years of experimental warming did not influence the thermal sensitivity of metabolic rate in the medaka fish Oryzias latipes

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    A pressing challenge is to determine whether and how global-change drivers influence species physiology and survival. Recently, researchers have proposed the metabolic theory of ecology, defending the hypothesis of a universal thermal dependence of metabolic rate or, alternatively, the metabolic cold adaptation theory, stating that local adaptation can influence the thermal sensitivity of metabolic rate. However, the long-term (i.e. multigenerational) consequences of warming for the thermal sensitivity of metabolic rate remain largely unexplored although it determines energy use and is crucial for species response to climate change. In this study, we used an evolutionary experiment with medaka fishes Oryzias latipes maintained for more than 12 generations at warm and cold temperatures (30 and 20°C, respectively) to address this issue. Our objective was to investigate whether thermal adaptation influences the relationship between temperature and mass-corrected metabolic rate and how this may occur. In agreement with the universal thermal dependence hypothesis, we found that warming did not significantly influence the thermal sensitivity of mass-corrected metabolic rate: neither the intercept nor the slope of the temperature–metabolic rate relationship differed among fish lineages. Our small-scale laboratory experiment thus indicated that there is limited potential for evolutionary change in medaka fish metabolic rate in response to warmer temperatures. Overall, we provide evidence that 9 years of experimental warming did not influence the thermal sensitivity of metabolic rate. Our results highlight the invariability of the thermal dependence of metabolic rate, which has important implications for adaptation to climate warming. This finding suggests a limited potential for metabolic adaptations in response to long-term temperature changes, which may have negative consequences for the persistence of fish populations under climate change

    Decreased expression of miR-29 family associated with autoimmune myasthenia gravis.

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    BACKGROUND: Myasthenia gravis (MG) is a rare autoimmune disease mainly mediated by autoantibodies against the acetylcholine receptor (AChR) at the neuromuscular junction. The thymus is the effector organ, and its removal alleviates the symptoms of the disease. In the early-onset form of MG, the thymus displays functional and morphological abnormalities such as B cell infiltration leading to follicular hyperplasia, and the production of AChR antibodies. Type-I interferon (IFN-I), especially IFN-β, is the orchestrator of thymic changes observed in MG. As Dicer and miR-29 subtypes play a role in modulating the IFN-I signalization in mouse thymus, we investigated their expression in MG thymus. METHODS: The expression of DICER and miR-29 subtypes were thoroughly investigated by RT-PCR in human control and MG thymuses, and in thymic epithelial cells (TECs). Using miR-29a/b-1-deficient mice, with lower miR-29a/b-1 expression, we investigated their susceptibility to experimental autoimmune MG (EAMG) as compared to wild-type mice. RESULTS: DICER mRNA and all miR-29 subtypes were down-regulated in the thymus of MG patients and DICER expression was correlated with the lower expression of miR-29a-3p. A decreased expression of miR-29 subtypes was similarly observed in MG TECs; a decrease also induced in TECs upon IFN-β treatment. We demonstrated that miR-29a/b-1-deficient mice were more susceptible to EAMG without higher levels of anti-AChR IgG subtypes. In the thymus, if no B cell infiltration was observed, an increased expression of Ifn-β associated with Baff expression and the differentiation of Th17 cells associated with increased expression of Il-6, Il-17a and Il-21 and decreased Tgf-β1 mRNA were demonstrated in miR-29a/b-1-deficient EAMG mice. CONCLUSIONS: It is not clear if the decreased expression of miR-29 subtypes in human MG is a consequence or a causative factor of thymic inflammation. However, our results from the EAMG mouse model indicated that a reduction in miR-29a/b1 may contribute to the pathophysiological process involved in MG by favoring the increased expression of IFN-β and the emergence of pro-inflammatory Th17 cells

    Tritiated Steel Micro-Particles: Computational Dosimetry and Prediction of Radiation-Induced DNA Damage for In Vitro Cell Culture Exposures.

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    Biological effects of radioactive particles can be experimentally investigated in vitro as a function of particle concentration, specific activity and exposure time. However, a careful dosimetric analysis is needed to elucidate the role of radiation emitted by radioactive products in inducing cyto- and geno-toxicity: the quantification of radiation dose is essential to eventually inform dose-risk correlations. This is even more fundamental when radioactive particles are short-range emitters and when they have a chemical speciation that might further concur to the heterogeneity of energy deposition at the cellular and sub-cellular level. To this aim, we need to use computational models. In this work, we made use of a Monte Carlo radiation transport code to perform a computational dosimetric reconstruction for in vitro exposure of cells to tritiated steel particles of micrometric size. Particles of this kind have been identified as worth of attention in nuclear power industry and research: tritium easily permeates in steel elements of nuclear reactor machinery, and mechanical operations on these elements (e.g., sawing) during decommissioning of old facilities can result in particle dispersion, leading to human exposure via inhalation. Considering the software replica of a representative in vitro setup to study the effect of such particles, we therefore modelled the radiation field due to the presence of particles in proximity of cells. We developed a computational approach to reconstruct the dose range to individual cell nuclei in contact with a particle, as well as the fraction of "hit" cells and the average dose for the whole cell population, as a function of particle concentration in the culture medium. The dosimetric analysis also provided the basis to make predictions on tritium-induced DNA damage: we estimated the dose-dependent expected yield of DNA double strand breaks due to tritiated steel particle radiation, as an indicator of their expected biological effectiveness
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