The Applegate mechanism in Post-Common-Envelope Binaries: Investigating the role of rotation

Eclipsing time variations (ETVs) are observed in many close binary systems. In particular, for several post-common-envelope binaries (PCEBs) that consist of a white dwarf and a main sequence star, the O-C diagram suggests that real or apparent orbital period variations are driven by Jupiter-mass planets or as a result of magnetic activity, the so-called Applegate mechanism. The latter explains orbital period variations as a result of changes in the stellar quadrupole moment due to magnetic activity. We explore the feasibility of driving ETVs via the Applegate mechanism for a sample of PCEB systems, including a range of different rotations. Using the MESA code we evolve 12 stars with different masses and rotation rates. We apply a simple dynamo model to their radial profiles to investigate on which scale the predicted activity cycle matches the observed modulation period, and quantify the uncertainty, and further calculate the required energies to drive que Applegate mechanism. We show that the Applegate mechanism is energetically feasible in 5 PCEB systems, and note that these are the systems with the highest rotation rate compared to the critical rotation rate of the main-sequence star. The results suggest that the ratio of physical to critical rotation in the main sequence star is an important indicator for the feasibility of Applegate's mechanism, but exploring larger samples will be necessary to probe this hypothesis.Comment: 9 pages, 5 figures. Accepted for publication in A&

Floquet theory for temporal correlations and spectra in time-periodic open quantum systems: Application to squeezed parametric oscillation beyond the rotating-wave approximation

Open quantum systems can display periodic dynamics at the classical level either due to external periodic modulations or to self-pulsing phenomena typically following a Hopf bifurcation. In both cases, the quantum fluctuations around classical solutions do not reach a quantum-statistical stationary state, which prevents adopting the simple and reliable methods used for stationary quantum systems. Here we put forward a general and efficient method to compute two-time correlations and corresponding spectral densities of time-periodic open quantum systems within the usual linearized (Gaussian) approximation for their dynamics. Using Floquet theory we show how the quantum Langevin equations for the fluctuations can be efficiently integrated by partitioning the time domain into one-period duration intervals, and relating the properties of each period to the first one. Spectral densities, like squeezing spectra, are computed similarly, now in a two-dimensional temporal domain that is treated as a chessboard with one-period x one-period cells. This technique avoids cumulative numerical errors as well as efficiently saves computational time. As an illustration of the method, we analyze the quantum fluctuations of a damped parametrically-driven oscillator (degenerate parametric oscillator) below threshold and far away from rotating-wave approximation conditions, which is a relevant scenario for modern low-frequency quantum oscillators. Our method reveals that the squeezing properties of such devices are quite robust against the amplitude of the modulation or the low quality of the oscillator, although optimal squeezing can appear for parameters that are far from the ones predicted within the rotating-wave approximation.Comment: Comments and constructive criticism are welcom

Protective Yeasts Control V. anguillarum Pathogenicity and Modulate the Innate Immune Response of Challenged Zebrafish (Danio rerio) Larvae

Indexación: Web of ScienceWe investigated mechanisms involved in the protection of zebrafish (Danio rerio) larvae by two probiotic candidate yeasts, Debaryornyces hansenii 97 (Dh97) and Yarrowia Iypolitica 242 (YI242), against a Vibrio anguillarum challenge. We determined the effect of different yeast concentrations (10(4)-10(7) CFU/mL) to: (i) protect larvae from the challenge, (ii) reduce the in vivo pathogen concentration and (iii) modulate the innate immune response of the host. To evaluate the role of zebrafish microbiota in protection, the experiments were performed in conventionally raised and germ free larvae. In vitro co-aggregation assays were performed to determine a direct yeast-pathogen interaction. Results showed that both yeasts significantly increased the survival rate of conventionally raised larvae challenged with V. anguillarum. The concentration of yeasts in larvae tended to increase with yeast inoculum, which was more pronounced for Dh97. Better protection was observed with Dh97 at a concentration of 106 CFU/mL compared to 104 CFU/mL. In germ-free conditions V anguillarum reached higher concentrations in larvae and provoked significantly more mortality than in conventional conditions, revealing the protective role of the host microbiota. Interestingly, yeasts were equally (Dh97) or more effective (YI242) in protecting germ-free than conventionally-raised larvae, showing that protection can be exerted only by yeasts and is not necessarily related to modulation of the host microbiota. Although none of the yeasts co aggregated with V anguillarum, they were able to reduce its proliferation in conventionally raised larvae, reduce initial pathogen concentration in germ-free larvae and prevent the upregulation of key components of the inflammatory/anti-inflammatory response (il1b, tnfa, c3, mpx, and il10, respectively). These results show that protection by yeasts of zebrafish larvae challenged with V anguillarum relates to an in vivo anti-pathogen effect, the modulation of the innate immune system, and suggests that yeasts avoid the host-pathogen interaction through mechanisms independent of co-aggregation. This study shows, for the first time, the protective role of zebrafish microbiota against V. anguillarum infection, and reveals mechanisms involved in protection by two non-Saccharomyces yeasts against this pathogen.http://journal.frontiersin.org/article/10.3389/fcimb.2016.00127/ful

Studying the role of the strawberry Fra protein family in the flavonoid metabolism during fruit ripening

Strawberry fruits are highly appreciated worldwide due to their pleasant flavor and aroma and to the health benefits associated to their consumption. An important part of these properties is due to their content in secondary metabolites, especially phenolic compounds, of which flavonoids are the most abundant in the strawberry fruit. Although the flavonoid biosynthesis pathway is uncovered, little is known about its regulation. The strawberry Fra a (Fra) genes constitute a large family of homologs of the major birch pollen allergen Bet v 1 and for which no equivalents exist in Arabidopsis. Our group has shown that Fra proteins are involved in the formation of colored compounds in strawberries (Muñoz et al., 2010), which mainly depends on the production of certain flavonoids; that they are structurally homologs to the PYR/PYL/RCAR Arabidopsis ABA receptor, and that they are able to bind flavonoids (Casañal et al., 2013). With these previous results, our working hypothesis is that the Fra proteins are involved in the regulation of the flavonoids pathway. They would mechanistically act as the ABA receptor, binding a protein interactor and a ligand to regulate a signaling cascade and/or act as molecular carriers. The main objective of this research is to characterize the Fra family in strawberry and gain insight into their role in the flavonoid metabolism. By RNAseq expression analysis in ripening fruits we have identified transcripts for 10 members of the Fra family. Although expressed in all tissues analyzed, each family member presents a unique pattern of expression, which suggests functional specialization for each Fra protein. Then, our next approach was to identify the proteins that interact with Fras and their ligands to gain knowledge on the role that these proteins play in the flavonoids pathway. To identify the interacting partners of Fras we have performed a yeast two hybrid (Y2H) screening against cDNA libraries of strawberry fruits at the green and red stages. A protein that shares a 95% homology to the Heat stress transcription factor A-4-C like of Fragaria vesca (HSA4C) interacts specifically with Fra1 and not with other family members, which suggests functional diversification of Fra proteins in specific signaling pathways. The Y2H screening is not yet saturated, so characterization of other interacting proteins with other members of the Fra family will shed light on the functional diversity within this gene family. This research will contribute to gain knowledge on how the flavonoid pathway, and hence, the fruit ripening, is regulated in strawberry; an economically important crop but for which basic research is still very limited. References: Muñoz, C, et al. (2010). The Strawberry Fruit Fra a Allergen Functions in Flavonoid Biosynthesis. Molecular Plant, 3(1): 113–124. Casañal, A, et al (2013). The Strawberry Pathogenesis-related 10 (PR-10) Fra a Proteins Control Flavonoid Biosynthesis by Binding Metabolic Intermediates. Journal of Biological Chemistry, 288(49): 35322–35332.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech

Enhancement of the immunoregulatory potency of mesenchymal stromal cells by treatment with immunosuppressive drugs

Background aims Multipotent mesenchymal stromal cells (MSCs) are distinguished by their ability to differentiate into a number of stromal derivatives of interest for regenerative medicine, but they also have immunoregulatory properties that are being tested in a number of clinical settings. Methods We show that brief incubations with rapamycin, everolimus, FK506 or cyclosporine A increase the immunosuppressive potency of MSCs and other cell types. Results The treated MSCs are up to 5-fold more potent at inhibiting the induced proliferation of T lymphocytes in vitro. We show that this effect probably is due to adsorption of the drug by the MSCs during pre-treatment, with subsequent diffusion into co-cultures at concentrations sufficient to inhibit T-cell proliferation. MSCs contain measurable amounts of rapamycin after a 15-min exposure, and the potentiating effect is blocked by a neutralizing antibody to the drug. With the use of a pre-clinical model of acute graft-versus-host disease, we demonstrate that a low dose of rapamycin-treated but not untreated umbilical cord–derived MSCs significantly inhibit the onset of disease. Conclusions The use of treated MSCs may achieve clinical end points not reached with untreated MSCs and allow for infusion of fewer cells to reduce costs and minimize potential side effects

Comparison of the Methods for the Background Reduction of Thick Targets in Routine PIXE Analysis

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Spontaneous symmetry breaking as a resource for noncritically squeezed light

In the last years we have proposed the use of the mechanism of spontaneous symmetry breaking with the purpose of generating perfect quadrature squeezing. Here we review previous work dealing with spatial (translational and rotational) symmetries, both on optical parametric oscillators and four-wave mixing cavities, as well as present new results. We then extend the phenomenon to the polarization state of the signal field, hence introducing spontaneous polarization symmetry breaking. Finally we propose a Jaynes-Cummings model in which the phenomenon can be investigated at the single-photon-pair level in a non-dissipative case, with the purpose of understanding it from a most fundamental point of view.Comment: Review for the proceedings of SPIE Photonics Europe. 11 pages, 5 figures

Editorial: Judgment and decision making under uncertainty. Descriptive, normative, and prescriptive perspectives

Judgment and Decision Making Under Uncertainty: Descriptive, Normative, and Prescriptive Perspectives was motivated by our interest in better understanding why people judge and decide as they do (descriptive perspective), how they ideally ought to judge and decide (normative perspective), and how their judgment and decision-making processes might be improved in practice (prescriptive perspective). We sought papers that addressed some aspect of judgment and decision making from one or more of these three theoretical perspectives. We further sought contributions that examined judgment and decision making under conditions of uncertainty, which we intentionally left loosely defined. Our focus on uncertainty reflects the fact that the vast majority of decisions people make in life are not made under conditions of complete certainty, and the uncertainties may be more or less well-defined. Indeed, different components of a single judgment or decision may have multiple uncertainties associated with it, some of which may be fuzzier than others. Following our call for papers, we received 32 submissions, 17 of which were accepted. The latter set comprises this book. There are 11 original research articles, 2 hypothesis and theory articles, 2 perspectives, and 1 book review and systematic review each

Metabolomic evaluation of Mitomycin C and rapamycin in a personalized treatment of pancreatic cancer

In a personalized treatment designed for a patient with pancreatic cancer resistant to other treatments, the success of Mitomycin C (MMC) has been highlighted. This was revealed in a murine xenograft tumor model encompassing pancreatic adenocarcinoma cells extracted from the patient. The patient was found to exhibit a biallelic inactivation of the PALB2 gene, involved in DNA repair in addition to another mutation in the TSC2 gene that induces susceptibility of the tumor to therapeutic targets of the PI3K-mTOR pathway. The aim of the study was to apply metabolomics to elucidate the modes of action of each therapy, suggesting why MMC was so successful in this patient and why it could be a more popular choice in future pancreatic cancer treatment. The effectiveness of MMC compared to rapamycin (RM), another relevant therapeutic agent has been evaluated through liquid- and gas-chromatography mass spectrometry-based metabolomic analyses of the xenograft tumors. The relative concentrations of many metabolites in the xenograft tumors were found to be increased by MMC relative to other treatments (RM and a combination of both), including a number that are involved in central carbon metabolism (CCM). Metabolic fingerprinting revealed statistically significantly altered pathways including, but not restricted to, the pentose phosphate pathway, glycolysis, TCA cycle, purine metabolism, fatty acid biosynthesis, in addition to many significant lipid and amino acid alterations. Given the genetic background of the patient, it was expected that the combined therapy would be most effective; however, the most effective was MMC alone. It is proposed that the effectiveness of MMC is owed to its direct effect on CCM, a vital region of tumor metabolism