5,964 research outputs found

    Analytical solution of axi-symmetrical lattice Boltzmann model for cylindrical Couette flows

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    Analytical solution for the axi-symmetrical lattice Boltzmann model is obtained for the low-Mach number cylindrical Couette flows. In the hydrodynamic limit, the present solution is in excellent agreement with the result of the Navier-Stokes equation. Since the kinetic boundary condition is used, the present analytical solution using nine discrete velocities can describe flows with the Knudsen number up to 0.1. Meanwhile, the comparison with the simulation data obtained by the direct simulation Monte Carlo method shows that higher-order lattice Boltzmann models with more discrete velocities are needed for highly rarefied flows

    Bioactive compounds from Rumex plants

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    Two new naphthalene acylglucosides, rumexneposides A (1) and B (2), together with 12 known compounds (3-14), were isolated from the roots of Rumex nepalensis. Their structures were established by chemical and spectroscopic methods. The biological activities of compounds 1-14 as well as an additional 11 compounds previously isolated from R. nepalensis and Rumex hastatus (15–25) were evaluated against Mycobacterium tuberculosis, para-aminobenzoic acid (pAba) pathway, and a panel of human cancer cell lines. The results showed that compound 15 was the most active against M. tuberculosis with an MIC value of 2.85 mM similar to that of isoniazid. Compound 5 could inhibit pAba synthetic pathway with an MIC value of 12.6 mM, comparable to that of positive control abyssomicin C, representing a new example of the rare pAba pathway inhibitors

    Adenosine-mono-phosphate-activated protein kinase-independent effects of metformin in T cells

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    The anti-diabetic drug metformin regulates T-cell responses to immune activation and is proposed to function by regulating the energy-stress-sensing adenosine-monophosphate-activated protein kinase (AMPK). However, the molecular details of how metformin controls T cell immune responses have not been studied nor is there any direct evidence that metformin acts on T cells via AMPK. Here, we report that metformin regulates cell growth and proliferation of antigen-activated T cells by modulating the metabolic reprogramming that is required for effector T cell differentiation. Metformin thus inhibits the mammalian target of rapamycin complex I signalling pathway and prevents the expression of the transcription factors c-Myc and hypoxia-inducible factor 1 alpha. However, the inhibitory effects of metformin on T cells did not depend on the expression of AMPK in T cells. Accordingly, experiments with metformin inform about the importance of metabolic reprogramming for T cell immune responses but do not inform about the importance of AMPK

    Responsiveness of voltage-gated calcium channels in SH-SY5Y human neuroblastoma cells on quasi-three-dimensional micropatterns formed with poly (l-lactic acid)

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    Introduction: In this study, quasi-three-dimensional (3D) microwell patterns were fabricated with poly (l-lactic acid) for the development of cell-based assays, targeting voltage-gated calcium channels (VGCCs). Methods and materials: SH-SY5Y human neuroblastoma cells were interfaced with the microwell patterns and found to grow as two dimensional (2D), 3D, and near two dimensional (N2D), categorized on the basis of the cells’ location in the pattern. The capability of the microwell patterns to support 3D cell growth was evaluated in terms of the percentage of the cells in each growth category. Cell spreading was analyzed in terms of projection areas under light microscopy. SH-SY5Y cells’ VGCC responsiveness was evaluated with confocal microscopy and a calcium fluorescent indicator, Calcium GreenTM-1. The expression of L-type calcium channels was evaluated using immunofluorescence staining with DM-BODIPY. Results: It was found that cells within the microwells, either N2D or 3D, showed more rounded shapes and less projection areas than 2D cells on flat poly (l-lactic acid) substrates. Also, cells in microwells showed a significantly lower VGCC responsiveness than cells on flat substrates, in terms of both response magnitudes and percentages of responsive cells, upon depolarization with 50 mM K+. This lower VGCC responsiveness could not be explained by the difference in L-type calcium channel expression. For the two patterns addressed in this study, N2D cells consistently exhibited an intermediate value of either projection areas or VGCC responsiveness between those for 2D and 3D cells, suggesting a correlative relation between cell morphology and VGCC responsiveness. Conclusion: These results suggest that the pattern structure and therefore the cell growth characteristics were critical factors in determining cell VGCC responsiveness and thus provide an approach for engineering cell functionality in cell-based assay systems and tissue engineering scaffolds

    How to Identify and Separate Bright Galaxy Clusters from the Low-frequency Radio Sky?

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    In this work we simulate the 5020050-200 MHz radio sky that is constrained in the field of view (55^{\circ} radius) of the 21 Centimeter Array (21CMA), by carrying out Monte-Carlo simulations to model redshifted cosmological reionization signals and strong contaminating foregrounds, including emissions from our Galaxy, galaxy clusters, and extragalactic point sources. As an improvement of previous works, we consider in detail not only random variations of morphological and spectroscopic parameters within the ranges allowed by multi-band observations, but also evolution of radio halos in galaxy clusters, assuming that relativistic electrons are re-accelerated in the ICM in merger events and lose energy via both synchrotron emission and inverse Compton scattering with CMB photons. By introducing a new approach designed on the basis of independent component analysis (ICA) and wavelet detection algorithm, we prove that, with a cumulative observation of one month with the 21CMA array, about 80%80\% of galaxy clusters with central brightness temperatures of >10 K> 10~{\rm K} at 65 MHz can be safely identified and separated from the overwhelmingly bright foreground. We find that the morphological and spectroscopic distortions are extremely small as compared to the input simulated clusters, and the reduced χ2\chi^2 of brightness temperature profiles and spectra are controlled to be 0.5\lesssim 0.5 and 1.3\lesssim 1.3, respectively. These results robustly indicate that in the near future a sample of dozens of bright galaxy clusters will be disentangled from the foreground in 21CMA observations, the study of which will greatly improve our knowledge about cluster merger rates, electron acceleration mechanisms in cluster radio halos, and magnetic field in the ICM.Comment: 35 pages, 10 figures, Accepted for publication in The Astrophysical Journa
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