Non-minimally coupled scalar field cosmology on the phase plane

In this publication we investigate dynamics of a flat FRW cosmological model with a non-minimally coupled scalar field with the coupling term $\xi R \psi^{2}$ in the scalar field action. The quadratic potential function $V(\psi)\propto \psi^{2}$ is assumed. All the evolutional paths are visualized and classified in the phase plane, at which the parameter of non-minimal coupling $\xi$ plays the role of a control parameter. The fragility of global dynamics with respect to changes of the coupling constant is studied in details. We find that the future big rip singularity appearing in the phantom scalar field cosmological models can be avoided due to non-minimal coupling constant effects. We have shown the existence of a finite scale factor singular point (future or past) where the Hubble function as well as its first cosmological time derivative diverges.Comment: revtex4, 20 pages, 12 figs; (v2) title changed, analysis of critical points at infinity added, accepted to JCA

ChunkitApp : Investigating the relevant units of online speech processing

Peer reviewe

Immunomodulation induced by synthetic peptides derived from Staphylococcus aureus protein A

Peptides from 10 to 22 amino acids containing sequences encompassed by Staphylococcus aureus protein A were synthesized. Some of these peptides, when present in cultures of lymphomononuclear cells from healthy donors or from cancer patients (melanoma, breast carcinoma, non-Hodgkin lymphoma and renal cell carcinoma) promoted: (i) changes in the phenotype of the lymphomononuclear population, (ii) stimulation of monocytes (release of IL-1 and TNF-alpha), and (iii) an increase in cytotoxicity against K562, Daudi and HT-29 cells. Isolated monocytes responded also to those peptides with a release of IL-1 and TNF alpha and an increase of cytotoxicity against HT-29 cells. It was found that the active peptides had the following structural pattern: a length of at least 15 amino-acid residues with a proline at position 6, valine, leucine, isoleucine, glycine, alanine or lysine at position 2, and glutamic or aspartic acid at position 11. Replacement of Pro at position 6 with any other residue turned the peptide inactive. Replacement of residues at positions 2 and 11 with amino-acid residues other than those required for activity resulted in compounds with a marked decrease in the immunomodulating properties described, or lacking these properties altogether

Candida albicans Inhibits Pseudomonas aeruginosa Virulence through Suppression of Pyochelin and Pyoverdine Biosynthesis.

Bacterial-fungal interactions have important physiologic and medical ramifications, but the mechanisms of these interactions are poorly understood. The gut is host to trillions of microorganisms, and bacterial-fungal interactions are likely to be important. Using a neutropenic mouse model of microbial gastrointestinal colonization and dissemination, we show that the fungus Candida albicans inhibits the virulence of the bacterium Pseudomonas aeruginosa by inhibiting P. aeruginosa pyochelin and pyoverdine gene expression, which plays a critical role in iron acquisition and virulence. Accordingly, deletion of both P. aeruginosa pyochelin and pyoverdine genes attenuates P. aeruginosa virulence. Heat-killed C. albicans has no effect on P. aeruginosa, whereas C. albicans secreted proteins directly suppress P. aeruginosa pyoverdine and pyochelin expression and inhibit P. aeruginosa virulence in mice. Interestingly, suppression or deletion of pyochelin and pyoverdine genes has no effect on P. aeruginosa's ability to colonize the GI tract but does decrease P. aeruginosa's cytotoxic effect on cultured colonocytes. Finally, oral iron supplementation restores P. aeruginosa virulence in P. aeruginosa and C. albicans colonized mice. Together, our findings provide insight into how a bacterial-fungal interaction can modulate bacterial virulence in the intestine. Previously described bacterial-fungal antagonistic interactions have focused on growth inhibition or colonization inhibition/modulation, yet here we describe a novel observation of fungal-inhibition of bacterial effectors critical for virulence but not important for colonization. These findings validate the use of a mammalian model system to explore the complexities of polymicrobial, polykingdom infections in order to identify new therapeutic targets for preventing microbial disease

Inducible nitric oxide synthase in human lymphomononuclear cells activated by synthetic peptides derived from extracellular matrix proteins.

Synthetic peptides with sequences present in extracellular matrix proteins are capable of causing the expression of the inducible form of nitric oxide synthase (iNOS), detected by immunocytochemistry, and the release of NO by human lymphomononuclear cells incubated in their presence. Active peptides are 15-mers containing a characteristic 2-6-11 motif in which the amino acid residue at position 2 is Leu, Ile, Val, Gly, Ala or Lys; the residue at position 6 is always Pro; and residue 11 is Glu or Asp. The induction of iNOS in human monocytes and macrophages could be involved in the cytotoxicity against tumor cell lines also elicited by these peptides

Exploring the Expanding Universe and Dark Energy using the Statefinder Diagnostic

The coming few years are likely to witness a dramatic increase in high quality Sn data as current surveys add more high redshift supernovae to their inventory and as newer and deeper supernova experiments become operational. Given the current variety in dark energy models and the expected improvement in observational data, an accurate and versatile diagnostic of dark energy is the need of the hour. This paper examines the Statefinder diagnostic in the light of the proposed SNAP satellite which is expected to observe about 2000 supernovae per year. We show that the Statefinder is versatile enough to differentiate between dark energy models as varied as the cosmological constant on the one hand, and quintessence, the Chaplygin gas and braneworld models, on the other. Using SNAP data, the Statefinder can distinguish a cosmological constant ($w=-1$) from quintessence models with $w \geq -0.9$ and Chaplygin gas models with $\kappa \leq 15$ at the $3\sigma$ level if the value of \om is known exactly. The Statefinder gives reasonable results even when the value of \om is known to only $\sim 20$ accuracy. In this case, marginalizing over \om and assuming a fiducial LCDM model allows us to rule out quintessence with $w \geq -0.85$ and the Chaplygin gas with $\kappa \leq 7$ (both at $3\sigma$). These constraints can be made even tighter if we use the Statefinders in conjunction with the deceleration parameter. The Statefinder is very sensitive to the total pressure exerted by all forms of matter and radiation in the universe. It can therefore differentiate between dark energy models at moderately high redshifts of z \lleq 10.Comment: 21 pages, 17 figures. Minor typos corrected to agree with version published in MNRAS. Results unchange

Scalar field cosmology in the energy phase-space -- unified description of dynamics

In this letter we apply dynamical system methods to study all evolutional paths admissible for all initial conditions of the FRW cosmological model with a non-minimally coupled to gravity scalar field and a barotropic fluid. We choose "energy variables" as phase variables. We reduce dynamics to a 3-dimensional dynamical system for an arbitrary potential of the scalar field in the phase space variables. After postulating the potential parameter $\Gamma$ as a function of $\lambda$ (defined as $-V'/V$) we reduce whole dynamics to a 3-dimensional dynamical system and study evolutional paths leading to current accelerating expansion. If we restrict the form of the potential then we will obtain a 2-dimensional dynamical system. We use the dynamical system approach to find a new generic quintessence scenario of approaching to the de Sitter attractor which appears only for the case of non-vanishing coupling constant.Comment: revtex4, 16 pages, 3 figs; (v2) refs. added, published versio

Cutaneous Biology: In vivo blockade of pemphigus vulgaris acantholysis by inhibition of intracellular signal transduction cascades

Pemphigus vulgaris (PV) is an autoimmune disease characterized by mucocutaneous intraepithelial blisters and pathogenic autoantibodies against desmoglein 3. The mechanism of blister formation in pemphigus has not been defined; however, in vitro data suggest a role for activation of intracellular signalling cascades. OBJECTIVES: To investigate the contribution of these signalling pathways to the mechanism of PV IgG-induced acantholysis in vivo. METHODS: We used the passive transfer mouse model. Mice were injected with IgG fractions of sera from a patient with PV, with or without pretreatment with inhibitors of proteins that mediate intracellular signalling cascades. RESULTS: Inhibitors of tyrosine kinases, phospholipase C, calmodulin and the serine/threonine kinase protein kinase C prevented PV IgG-induced acantholysis in vivo. CONCLUSIONS: These observations strongly support the role of intracellular signalling cascades in the molecular mechanism of PV IgG-induced acantholysi

An approach to the toxicity and toxicokinetics of aflatoxin B1 and ochratoxin A after simultaneous oral administration to fasted F344 rats

Humans are exposed to the hepatotoxic aflatoxin B1 (AFB1) and nephrotoxic ochratoxin A (OTA) through diet. However, kinetic and toxicological data after their co-administration are scarce. In this study, a single oral dose of AFB1 (0.25mg/kg bw)+OTA (0.5mg/kgbw) was administered to fasted F344 rats. Blood, liver and kidney were harvested at different timepoints for mycotoxins quantification, relative weight calculation, clinical biochemistry and histopathology analysis. Toxicity parameters pointed to acute toxicity in liver due to AFB1. No remarkable toxicity was observed in kidneys or immunological organs. Maximum observed concentrations in plasma (C(max)) were at 10min and 2h for AFB1 and OTA, respectively. AFB1 plasma concentration could indicate a rapid absorption/ metabolism of the mycotoxin; and AFB1 liver and kidney concentrations were lower than LOQ and LOD, respectively. For OTA, C(max) was 4326.2μg/L in plasma. In kidney and liver C(max) was reached at 8h and concentrations were very similar between both organs at all timepoints. Due to the low levels of AFB1, the effect of OTA on AFB1 kinetics could not be assessed. However, AFB1 seems not to affect OTA kinetics, as its profile seems very similar to kinetic studies performed only with OTA in similar conditions

Size effects in the structural phase transition of VO2 nanoparticles

We have observed size effects in the structural phase transition of submicron vanadium dioxide precipitates in silica. The VO2 nanoprecipitates are produced by the stoichiometric coimplantation of vanadium and oxygen and subsequent thermal processing. The observed size dependence in the transition temperature and hysteresis loops of the semiconductor-to-metal phase transition in VO2 is described in terms of heterogeneous nucleation statistics with a phenomenological approach in which the density of nucleating defects is a power function of the driving force