3,519 research outputs found

    Myeloid dendritic cells display downregulation of C-type lectin receptors and aberrant lectin uptake in systemic lupus erythematosus

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    Abstract Introduction There is a growing body of evidence implicating aberrant dendritic cell function as a crucial component in the immunopathogenesis of systemic lupus erythematosus. The purpose of the present study was to characterize the phagocytic capacity and expression of receptors involved in pathogen recognition and self-nonself discrimination on myeloid dendritic cells from patients with lupus. Methods Unstimulated or stimulated monocyte-derived dendritic cells were obtained from lupus patients and healthy control individuals, and expression of C-type lectin receptors (mannose receptor and dendritic cell-specific intercellular adhesion molecule-grabbing nonintegrin), complement-receptor 3 and Fcγ receptors was determined by flow cytometry. Dextran uptake by lupus and control dendritic cells was also assessed by flow cytometry. Serum IFNγ was quantified by ELISA, and uptake of microbial products was measured using fluorescently labeled zymosan. Results When compared with dendritic cells from healthy control individuals, unstimulated and stimulated lupus dendritic cells displayed significantly decreased dextran uptake and mannose receptor and dendritic cell-specific intercellular adhesion molecule-grabbing nonintegrin expression. Decreased expression of the mannose receptor was associated with high serum IFNγ levels, but not with maturation status or medications. Diminished dextran uptake and mannose receptor expression correlated with lupus disease activity. There were no differences between control and lupus dendritic cells in the expression of other pattern recognition receptors or in the capacity to uptake zymosan particles Conclusions Lupus dendritic cells have diminished endocytic capacity, which correlates with decreased mannose receptor expression. While this phenomenon appears primarily intrinsic to dendritic cells, modulation by serum factors such as IFNγ could play a role. These abnormalities may be relevant to the aberrant immune homeostasis and the increased susceptibility to infections described in lupus.http://deepblue.lib.umich.edu/bitstream/2027.42/112498/1/13075_2008_Article_2366.pd

    Lattice Heavy Quark Effective Theory and the Isgur-Wise function

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    We compute the Isgur-Wise function using heavy quark effective theory formulated on the lattice. The non-relativistic kinetic energy term of the heavy quark is included to the action as well as terms remaining in the infinite quark mass limit. The classical velocity of the heavy quark is renormalized on the lattice and we determine the renormalized velocity non-perturbatively using the energy-momentum dispersion relation. The slope parameter of the Isgur-Wise function at zero recoil is obtained at β=6.0\beta=6.0 on a 243×4824^3\times 48 lattice for three values of mQm_{Q}.Comment: 14 pages of A4 format and 8 figures in one uuencoded postscript fil

    Real-space renormalization group approach for the corner Hamiltonian

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    We present a real-space renormalization group approach for the corner Hamiltonian, which is relevant to the reduced density matrix in the density matrix renormalization group. A set of self-consistent equations that the renormalized Hamiltonian should satisfy in the thermodynamic limit is also derived from the fixed point of the recursion relation for the corner Hamiltonian. We demonstrate the renormalization group algorithm for the S=1/2S=1/2 XXZ spin chain and show that the results are consistent with the exact solution. We further examine the renormalization group for the S=1 Heisenberg spin chain and then discuss the nature of the eigenvalue spectrum of the corner Hamiltonian for the non-integrable model.Comment: 7 page

    BB Decay Constants from NRQCD with Dynamical Fermions

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    We present a lattice investigation of the heavy-light meson decay constants using Wilson light quarks and NRQCD heavy quarks, partially including the effects of dynamical sea quarks. We calculate the pseudoscalar and vector decay constants over a wide range in heavy quark mass and are able to perform a detailed analysis of heavy quark symmetry. We find consistency between the extrapolation of the NRQCD results and the static case, as expected. We find the slope of the decay constants with 1/M1/M is significantly larger than naive expectations and the results of previous lattice calculations. For the first time we extract the non-perturbative coefficients of the slope arising from the O(1/M)O(1/M) heavy quark interactions separately and show the kinetic energy of the heavy quark is dominant and responsible for the large slope. In addition, we find that significant systematic errors remain in the decay constant extracted around the BB meson mass due to truncating the NRQCD series at O(1/M)O(1/M). We estimate the higher order contributions to fBf_B are approximately 20%20\%; roughly the same size as the systematic errors introduced by using the Wilson action for light quarks.Comment: 30 pages, Latex, 14 postscript figure

    Ab Initio Calculation of Relativistic Corrections to the Static Interquark potential I: SU(2) Gauge Theory

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    We test the capability of state-of-the-art lattice techniques for a precise determination of relativistic corrections to the static interquark potential, by use of SU(2) gauge theory. Emphasis is put on the short range structure of the spin dependent potentials, with lattice resolution a ranging from a approx 0.04 fm (at beta=2.74) down to a approx 0.02 fm (at beta=2.96) on volumes of 32^4 and 48^4 lattice sites. We find a new short range Coulomb-like contribution to the spin-orbit potential V_1'.Comment: 37 pages REVTeX with 20 encapsuled ps figure

    EvoL: The new Padova T-SPH parallel code for cosmological simulations - I. Basic code: gravity and hydrodynamics

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    We present EvoL, the new release of the Padova N-body code for cosmological simulations of galaxy formation and evolution. In this paper, the basic Tree + SPH code is presented and analysed, together with an overview on the software architectures. EvoL is a flexible parallel Fortran95 code, specifically designed for simulations of cosmological structure formation on cluster, galactic and sub-galactic scales. EvoL is a fully Lagrangian self-adaptive code, based on the classical Oct-tree and on the Smoothed Particle Hydrodynamics algorithm. It includes special features such as adaptive softening lengths with correcting extra-terms, and modern formulations of SPH and artificial viscosity. It is designed to be run in parallel on multiple CPUs to optimize the performance and save computational time. We describe the code in detail, and present the results of a number of standard hydrodynamical tests.Comment: 33 pages, 49 figures, accepted on A&

    Mesonic correlation lengths in high-temperature QCD

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    We consider spatial correlation lengths \xi for various QCD light quark bilinears at temperatures above a few hundred MeV. Some of the correlation lengths (such as that related to baryon density) coincide with what has been measured earlier on from glueball-like states; others do not couple to glueballs, and have a well-known perturbative leading-order expression as well as a computable next-to-leading-order correction. We determine the latter following analogies with the NRQCD effective theory, used for the study of heavy quarkonia at zero temperature: we find (for the quenched case) \xi^{-1} = 2 \pi T + 0.1408 g^2 T, and compare with lattice results. One manifestation of U_A(1) symmetry non-restoration is also pointed out.Comment: 25 pages. v2: small clarifications; published versio

    The Heavy Hadron Spectrum

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    I discuss the spectrum of hadrons containing heavy quarks (bb or cc), and how well the experimental results are matched by theoretical ideas. Useful insights come from potential models and applications of Heavy Quark Symmetry and these can be compared with new numerical results from the ab initio methods of Lattice QCD.Comment: 64 pages, Latex, lectures at Schladming Winter School 199

    Characterization and genomic analysis of chromate resistant and reducing Bacillus cereus strain SJ1

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    <p>Abstract</p> <p>Background</p> <p>Chromium is a toxic heavy metal, which primarily exists in two inorganic forms, Cr(VI) and Cr(III). Chromate [Cr(VI)] is carcinogenic, mutational, and teratogenic due to its strong oxidizing nature. Biotransformation of Cr(VI) to less-toxic Cr(III) by chromate-resistant and reducing bacteria has offered an ecological and economical option for chromate detoxification and bioremediation. However, knowledge of the genetic determinants for chromate resistance and reduction has been limited so far. Our main aim was to investigate chromate resistance and reduction by <it>Bacillus cereus </it>SJ1, and to further study the underlying mechanisms at the molecular level using the obtained genome sequence.</p> <p>Results</p> <p><it>Bacillus cereus </it>SJ1 isolated from chromium-contaminated wastewater of a metal electroplating factory displayed high Cr(VI) resistance with a minimal inhibitory concentration (MIC) of 30 mM when induced with Cr(VI). A complete bacterial reduction of 1 mM Cr(VI) was achieved within 57 h. By genome sequence analysis, a putative chromate transport operon, <it>chrIA</it>1, and two additional <it>chrA </it>genes encoding putative chromate transporters that likely confer chromate resistance were identified. Furthermore, we also found an azoreductase gene <it>azoR </it>and four nitroreductase genes <it>nitR </it>possibly involved in chromate reduction. Using reverse transcription PCR (RT-PCR) technology, it was shown that expression of adjacent genes <it>chrA</it>1 and <it>chrI </it>was induced in response to Cr(VI) but expression of the other two chromate transporter genes <it>chrA</it>2 and <it>chrA</it>3 was constitutive. In contrast, chromate reduction was constitutive in both phenotypic and gene expression analyses. The presence of a resolvase gene upstream of <it>chrIA</it>1, an arsenic resistance operon and a gene encoding Tn7-like transposition proteins ABBCCCD downstream of <it>chrIA</it>1 in <it>B. cereus </it>SJ1 implied the possibility of recent horizontal gene transfer.</p> <p>Conclusion</p> <p>Our results indicate that expression of the chromate transporter gene <it>chrA</it>1 was inducible by Cr(VI) and most likely regulated by the putative transcriptional regulator ChrI. The bacterial Cr(VI)-resistant level was also inducible. The presence of an adjacent arsenic resistance gene cluster nearby the <it>chrIA</it>1 suggested that strong selective pressure by chromium and arsenic could cause bacterial horizontal gene transfer. Such events may favor the survival and increase the resistance level of <it>B. cereus </it>SJ1.</p

    Complete O(v^2) corrections to the static interquark potential from SU(3) gauge theory

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    For the first time, we determine the complete spin- and momentum-dependent order v^2 corrections to the static interquark potential from simulations of QCD in the valence quark approximation at inverse lattice spacings of 2-3 GeV. A new flavor dependent correction to the central potential is found. We report a 1/r^2 contribution to the long range spin-orbit potential V_1'. The other spin-dependent potentials turn out to be short ranged and can be well understood by means of perturbation theory. The momentum-dependent potentials qualitatively agree with minimal area law expectations. In view of spectrum calculations, we discuss the matching of the effective nonrelativistic theory to QCD as well as renormalization of lattice results. In a first survey of the resulting bottomonia and charmonia spectra we reproduce the experimental levels within average errors of 12.5 MeV and 22 MeV, respectively.Comment: 54 pages REVTeX with 24 encapsuled ps figure
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