1,120 research outputs found
Observation of isotonic symmetry for enhanced quadrupole collectivity in neutron-rich 62,64,66Fe isotopes at N=40
The transition rates for the 2_{1}^{+} states in 62,64,66Fe were studied
using the Recoil Distance Doppler-Shift technique applied to projectile Coulomb
excitation reactions. The deduced E2 strengths illustrate the enhanced
collectivity of the neutron-rich Fe isotopes up to N=40. The results are
interpreted by the generalized concept of valence proton symmetry which
describes the evolution of nuclear structure around N=40 as governed by the
number of valence protons with respect to Z~30. The deformation suggested by
the experimental data is reproduced by state-of-the-art shell calculations with
a new effective interaction developed for the fpgd valence space.Comment: 4 pages, 2 figure
The Cyclophilin-Binding Agent Sanglifehrin A Is a Dendritic Cell Chemokine and Migration Inhibitor
Sanglifehrin A (SFA) is a cyclophilin-binding immunosuppressant but the immunobiology of action is poorly understood. We and others have reported that SFA inhibits IL-12 production and antigen uptake in dendritic cells (DC) and exhibits lower activity against lymphocytes. Here we show that SFA suppresses DC chemokine production and migration. Gene expression analysis and subsequent protein level confirmation revealed that SFA suppressed CCL5, CCL17, CCL19, CXCL9 and CXCL10 expression in human monocyte-derived DC (moDC). A systems biology analysis, Onto Express, confirmed that SFA interferes with chemokine-chemokine receptor gene expression with the highest impact. Direct comparison with the related agent cyclosporine A (CsA) and dexamethasone indicated that SFA uniquely suppresses moDC chemokine expression. Competitive experiments with a 100-fold molar excess of CsA and with N-Methyl-Val-4-cyclosporin, representing a nonimmunosuppressive derivative of CsA indicated chemokine suppression through a cyclophilin-A independent pathway. Functional assays confirmed reduced migration of CD4+ Tcells and moDCs to supernatant of SFA-exposed moDCs. Vice versa, SFA-exposed moDC exhibited reduced migration against CCL19. Moreover, SFA suppressed expression of the ectoenzyme CD38 that was reported to regulate DC migration and cytokine production. These results identify SFA as a DC chemokine and migration inhibitor and provide novel insight into the immunobiology of SFA
Lifetime measurements in Co and Co
Lifetimes of the and states in Co and the
state in Co were measured using the recoil distance Doppler
shift and the differential decay curve methods. The nuclei were populated by
multi-nucleon transfer reactions in inverse kinematics. Gamma rays were
measured with the EXOGAM Ge array and the recoiling fragments were fully
identified using the large-acceptance VAMOS spectrometer. The E2 transition
probabilities from the and states to the ground
state could be extracted in Co as well as an upper limit for the
(E2) value in Co. The experimental
results were compared to large-scale shell-model calculations in the and
model spaces, allowing to draw conclusions on the single-particle
or collective nature of the various states.Comment: 8 pages, 8 figures, 1 table, accepted for publication in Physical
Review
Structure of Fat Jets at the Tevatron and Beyond
Boosted resonances is a highly probable and enthusiastic scenario in any
process probing the electroweak scale. Such objects when decaying into jets can
easily blend with the cornucopia of jets from hard relative light QCD states.
We review jet observables and algorithms that can contribute to the
identification of highly boosted heavy jets and the possible searches that can
make use of such substructure information. We also review previous studies by
CDF on boosted jets and its measurements on specific jet shapes.Comment: invited review for a special "Top and flavour physics in the LHC era"
issue of The European Physical Journal C, we invite comments regarding
contents of the review; v2 added references and institutional preprint
number
Diboson-Jets and the Search for Resonant Zh Production
New particles at the TeV-scale may have sizeable decay rates into boosted
Higgs bosons or other heavy scalars. Here, we investigate the possibility of
identifying such processes when the Higgs/scalar subsequently decays into a
pair of W bosons, constituting a highly distinctive "diboson-jet." These can
appear as a simple dilepton (plus MET) configuration, as a two-prong jet with
an embedded lepton, or as a four-prong jet. We study jet substructure methods
to discriminate these objects from their dominant backgrounds. We then
demonstrate the use of these techniques in the search for a heavy spin-one Z'
boson, such as may arise from strong dynamics or an extended gauge sector,
utilizing the decay chain Z' -> Zh -> Z(WW^(*)). We find that modes with
multiple boosted hadronic Zs and Ws tend to offer the best prospects for the
highest accessible masses. For 100/fb luminosity at the 14 TeV LHC, Z' decays
into a standard 125 GeV Higgs can be observed with 5-sigma significance for
masses of 1.5-2.5 TeV for a range of models. For a 200 GeV Higgs (requiring
nonstandard couplings, such as fermiophobic), the reach may improve to up to
2.5-3.0 TeV.Comment: 23 pages plus appendices, 9 figure
Heavy Squarks at the LHC
The LHC, with its seven-fold increase in energy over the Tevatron, is capable
of probing regions of SUSY parameter space exhibiting qualitatively new
collider phenomenology. Here we investigate one such region in which first
generation squarks are very heavy compared to the other superpartners. We find
that the production of these squarks, which is dominantly associative, only
becomes rate-limited at mSquark > 4(5) TeV for L~10(100) fb-1. However,
discovery of this scenario is complicated because heavy squarks decay primarily
into a jet and boosted gluino, yielding a dijet-like topology with missing
energy (MET) pointing along the direction of the second hardest jet. The result
is that many signal events are removed by standard jet/MET anti-alignment cuts
designed to guard against jet mismeasurement errors. We suggest replacing these
anti-alignment cuts with a measurement of jet substructure that can
significantly extend the reach of this channel while still removing much of the
background. We study a selection of benchmark points in detail, demonstrating
that mSquark= 4(5) TeV first generation squarks can be discovered at the LHC
with L~10(100)fb-1
Sphingosine 1-phosphate modulates antigen capture by murine langerhans cells via the S1P2 receptor subtype
Dendritic cells (DCs) play a pivotal role in the development of cutaneous contact hypersensitivity (CHS) and atopic dermatitis as they capture and process antigen and present it to T lymphocytes in the lymphoid organs. Recently, it has been indicated that a topical application of the sphingolipid sphingosine 1-phosphate (S1P) prevents the inflammatory response in CHS, but the molecular mechanism is not fully elucidated. Here we indicate that treatment of mice with S1P is connected with an impaired antigen uptake by Langerhans cells (LCs), the initial step of CHS. Most of the known actions of S1P are mediated by a family of five specific G protein-coupled receptors. Our results indicate that S1P inhibits macropinocytosis of the murine LC line XS52 via S1P2 receptor stimulation followed by a reduced phosphatidylinositol 3-kinase (PI3K) activity. As down-regulation of S1P2 not only diminished S1P-mediated action but also enhanced the basal activity of LCs on antigen capture, an autocrine action of S1P has been assumed. Actually, S1P is continuously produced by LCs and secreted via the ATP binding cassette transporter ABCC1 to the extracellular environment. Consequently, inhibition of ABCC1, which decreased extracellular S1P levels, markedly increased the antigen uptake by LCs. Moreover, stimulation of sphingosine kinase activity, the crucial enzyme for S1P formation, is connected not only with enhanced S1P levels but also with diminished antigen capture. These results indicate that S1P is essential in LC homeostasis and influences skin immunity. This is of importance as previous reports suggested an alteration of S1P levels in atopic skin lesions
Human MAIT cells respond to and suppress HIV-1
Human MAIT cells sit at the interface between innate and adaptive immunity, are polyfunctional and are capable of killing pathogen infected cells via recognition of the Class IB molecule MR1. MAIT cells have recently been shown to possess an antiviral protective role in vivo and we therefore sought to explore this in relation to HIV-1 infection. There was marked activation of MAIT cells in vivo in HIV-1-infected individuals, which decreased following ART. Stimulation of THP1 monocytes with R5 tropic HIVBAL potently activated MAIT cells in vitro. This activation was dependent on IL-12 and IL-18 but was independent of the TCR. Upon activation, MAIT cells were able to upregulate granzyme B, IFNγ and HIV-1 restriction factors CCL3, 4, and 5. Restriction factors produced by MAIT cells inhibited HIV-1 infection of primary PBMCs and immortalized target cells in vitro. These data reveal MAIT cells to be an additional T cell population responding to HIV-1, with a potentially important role in controlling viral replication at mucosal sites
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