3,003 research outputs found
Vector mesons in systems
A new selection rule is described for the vector mesons in the decuplet
representations of flavor SU(3)Comment: 7 pages and 1 figur
The ALICE CPV Detector
The Charged-Particle Veto (CPV) detector of ALICE at the LHC is presented. Physics motivation for the detector, its construction and operation in physics runs are shortly discussed. Readout electronics and data taking conditions are described. Special attention is focused on CPV automation via the detector control system. Different states of the detector and protection algorithms implemented into the control system are described
Formation of Centauro and Strangelets in Nucleus-Nucleus Collisions at the LHC and their Identification by the ALICE Experiment
We present a phenomenological model which describes the formation of a
Centauro fireball in nucleus-nucleus interactions in the upper atmosphere and
at the LHC, and its decay to non-strange baryons and Strangelets. We describe
the CASTOR detector for the ALICE experiment at the LHC. CASTOR will probe, in
an event-by-event mode, the very forward, baryon-rich phase space 5.6 < \eta <
7.2 in 5.5 A TeV central Pb + Pb collisions. We present results of simulations
for the response of the CASTOR calorimeter, and in particular to the traversal
of Strangelets.Comment: 4 pages, 4 figures, to appear in the proceedings of the 26th ICR
CASTOR: Centauro and Strange Object Research in nucleus-nucleus collisions at LHC
We describe the CASTOR detector designed to probe the very forward,
baryon-rich rapidity region in nucleus-nucleus collisions at the LHC. We
present a phenomenological model describing the formation of a QGP fireball in
a high baryochemical potential environment, and its subsequent decay into
baryons and strangelets. The model explains Centauros and the long-penetrating
component and makes predictions for the LHC.
Simulations of Centauro-type events were done. To study the response of the
apparatus to new effects different exotic species (DCC, Centauros, strangelets
etc.) were passed through the deep calorimeter. The energy deposition pattern
in the calorimeter appears to be a new clear signature of the QGP.Comment: Talk given by E. Gladysz-Dziadus for the CASTOR group, Intern.
Workshop on Nuclear Theory, 10-15 June, 2002, Bulgaria, Rila Mountains, 15
pages, 14 figure
Proposed Search for Mixing in Polarization Phenomena
The and meson mass difference induces the mixing of the
and resonances, the amplitude of which, between the
and thresholds, is large in magnitude, of the order of , and possesses the
phase sharply varying by about 90. We suggest performing the polarized
target experiments on the reaction at high energy in
which the fact of the existence of mixing can be
unambiguously and very easily established through the presence of a strong jump
in the azimuthal asymmetry of the wave production cross section
near the thresholds. The presented estimates of the polarization
effect to be expected in experiment are to a great extent model independent.Comment: RevTeX, 9 pages, 1 figure. A number of typographical and grammatical
errors correcte
Model of Centauro and strangelet production in heavy ion collisions
We discuss the phenomenological model of Centauro event production in
relativistic nucleus-nucleus collisions. This model makes quantitative
predictions for kinematic observables, baryon number and mass of the Centauro
fireball and its decay products. Centauros decay mainly to nucleons, strange
hyperons and possibly strangelets. Simulations of Centauro events for the
CASTOR detector in Pb-Pb collisions at LHC energies are performed. The
signatures of these events are discussed in detail.Comment: 19 pages, LaTeX+revtex4, 14 eps-figures and 3 table
Human Placental Syncytiotrophoblasts Restrict Toxoplasma gondii Attachment and Replication and Respond to Infection by Producing Immunomodulatory Chemokines
Toxoplasma gondii is a major source of congenital disease worldwide, but the cellular and molecular factors associated with its vertical transmission are largely unknown. In humans, the placenta forms the key interface between the maternal and fetal compartments and forms the primary barrier that restricts the hematogenous spread of microorganisms. Here, we utilized primary human trophoblast (PHT) cells isolated from full-term placentas and human midgestation chorionic villous explants to determine the mechanisms by which human trophoblasts restrict and respond to T. gondii infection. We show that placental syncytiotrophoblasts, multinucleated cells that are in direct contact with maternal blood, restrict T. gondii infection at two distinct stages of the parasite lytic cycle—at the time of attachment and also during intracellular replication. Utilizing comparative transcriptome sequencing (RNA-seq) transcriptional profiling, we also show that human placental trophoblasts from both the second and third trimesters respond uniquely to T. gondii infection compared to trophoblast cell lines, typified by the upregulation of several immunity-related genes. One of the most differentially induced genes was the chemokine CCL22, which relies on the secretion of a parasite effector(s) either during or after invasion for its induction. Collectively, our findings provide new insights into the mechanisms by which the human placenta restricts the vertical transmission of T. gondii at early and late stages of human pregnancy and demonstrate the existence of at least two interferon-independent pathways that restrict T. gondii access to the fetal compartment.
IMPORTANCE Toxoplasma gondii is a major source of congenital disease worldwide and must breach the placental barrier to be transmitted from maternal blood to the developing fetus. The events associated with the vertical transmission of T. gondii are largely unknown. Here, we show that primary human syncytiotrophoblasts, the fetus-derived cells that comprise the primary placental barrier, restrict T. gondii infection at two distinct stages of the parasite life cycle and respond to infection by inducing a unique immunomodulatory transcriptional profile. Collectively, our findings provide important insights into the mechanisms by which human syncytiotrophoblasts restrict T. gondii infection at early and late stages of human pregnancy, identify both permissive and resistant human placental cell types, and identify the placenta-enriched signaling pathways induced in response to infection
The Expression and Localization of N-Myc Downstream-Regulated Gene 1 in Human Trophoblasts
The protein N-Myc downstream-regulated gene 1 (NDRG1) is implicated in the regulation of cell proliferation, differentiation, and cellular stress response. NDRG1 is expressed in primary human trophoblasts, where it promotes cell viability and resistance to hypoxic injury. The mechanism of action of NDRG1 remains unknown. To gain further insight into the intracellular action of NDRG1, we analyzed the expression pattern and cellular localization of endogenous NDRG1 and transfected Myc-tagged NDRG1 in human trophoblasts exposed to diverse injuries. In standard conditions, NDRG1 was diffusely expressed in the cytoplasm at a low level. Hypoxia or the hypoxia mimetic cobalt chloride, but not serum deprivation, ultraviolet (UV) light, or ionizing radiation, induced the expression of NDRG1 in human trophoblasts and the redistribution of NDRG1 into the nucleus and cytoplasmic membranes associated with the endoplasmic reticulum (ER) and microtubules. Mutation of the phosphopantetheine attachment site (PPAS) within NDRG1 abrogated this pattern of redistribution. Our results shed new light on the impact of cell injury on NDRG1 expression patterns, and suggest that the PPAS domain plays a key role in NDRG1's subcellular distribution. © 2013 Shi et al
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