A search for X-rays from UV Ceti flare stars

A search of MIT/OSO-7 data was made for evidence of X-ray emission from flares of UV Ceti flare stars. Observations from McDonald Observatory were used to identify the times of optical flares. The only instance of coincident coverage occurred on 1974 January 21 UT at 03:43:26 GMT for delta m(u)=0.86 flare of YZ CMi. No radio coverage of this particular event was obtained. Upper limits (3 sigma) of 0.8, 1.0, and 0.7 photons/sq cm-sec on the observed X-ray flux were set for the energy ranges greater than or approximately equal to 15, greater than or approximately equal to 3, and 1-10 keV, respectively

Quantitative Determination of the Adiabatic Condition Using Force-Detected Nuclear Magnetic Resonance

The adiabatic condition governing cyclic adiabatic inversion of proton spins in a micron-sized ammonium chloride crystal was studied using room temperature nuclear magnetic resonance force microscopy. A systematic degradation of signal-to-noise was observed as the adiabatic condition became violated. A theory of adiabatic following applicable to cyclic adiabatic inversion is reviewed and implemented to quantitatively determine an adiabaticity threshold $(\gamma H_1)^2/(\omega_{osc}\Omega) = 6.0$ from our experimental results.Comment: 5 pages, 3 fig

Neutrophil Oxygen Radical Production by Dialysis Membranes

The ability of different dialysis membranes to activate polymorphonuclear neutrophil oxygen radical production was investigated with chemiluminescence. All the six membranes, namely cuprophan, cellulose acetate, polycarbonate, polysulphone, polyacrilonitrile and polymethylmethacrylate were able to interact with neutrophils and stimulate their oxygen radical production, the highest responses being seen with polyacrilonitrile, polymethylmethacrylate and polycarbonate. To analyse the role of complement in this interaction, fresh plasma, heat inactivated and zymosan-activated plasma were added: with fresh plasma oxygen radical production was stimulated on cuprophan, cellulose acetate and polysulphone, not modified on polycarbonate, and decreased on polyacrilonitrile and polymethylmethacrylate. With heat-inactivated plasma, the responses were decreased or abrogated on all the membranes except polycarbonate and polymethylmethacrylate, whereas with zymosanactivated plasma similar responses to fresh plasma were observed. In addition, when plasma was used to precoat the membrane, cuprophan, cellulose acetate and polysulphone disclosed an enhanced neutrophil oxidative burst, while precoated polyacrilonitrile and polymethylmethacrylate were less stimulatory than uncoated membranes. In contrast the precoating of polycarbonate did not modify oxygen radical production. These data suggest that neutrophil activation occurs by direct membrane neutrophil interaction. Plasmatic factors modulate this interaction but complement seems involved on cellulosic and polysulphone membranes only. Therefore, it appears that oxygen radicals produced from contact of neutrophils with the dialysis membrane might play an initial and/or additional role in the events occurring at the initiation of haemodialysi

Cancer metabolism at a glance

A defining hallmark of cancer is uncontrolled cell proliferation. This is initiated once cells have accumulated alterations in signaling pathways that control metabolism and proliferation, wherein the metabolic alterations provide the energetic and anabolic demands of enhanced cell proliferation. How these metabolic requirements are satisfied depends, in part, on the tumor microenvironment, which determines the availability of nutrients and oxygen. In this Cell Science at a Glance paper and the accompanying poster, we summarize our current understanding of cancer metabolism, emphasizing pathways of nutrient utilization and metabolism that either appear or have been proven essential for cancer cells. We also review how this knowledge has contributed to the development of anticancer therapies that target cancer metabolism

Thymus transplantation for complete DiGeorge syndrome: European experience

Background: Thymus transplantation is a promising strategy for the treatment of athymic complete DiGeorge syndrome (cDGS). Methods: Twelve patients with cDGS were transplanted with allogeneic cultured thymus. Objective: To confirm and extend the results previously obtained in a single centre. Results: Two patients died of pre-existing viral infections without developing thymopoeisis and one late death occurred from autoimmune thrombocytopaenia. One infant suffered septic shock shortly after transplant resulting in graft loss and the need for a second transplant. Evidence of thymopoeisis developed from 5-6 months after transplantation in ten patients. The median (range) of circulating naïve CD4 counts (x10663 /L) were 44(11-440) and 200(5-310) at twelve and twenty-four months post-transplant and T-cell receptor excision circles were 2238 (320-8807) and 4184 (1582 -24596) per106 65 T-cells. Counts did not usually reach normal levels for age but patients were able to clear pre-existing and later acquired infections. At a median of 49 months (22-80), eight have ceased prophylactic antimicrobials and five immunoglobulin replacement. Histological confirmation of thymopoeisis was seen in seven of eleven patients undergoing biopsy of transplanted tissue including five showing full maturation through to the terminal stage of Hassall body formation. Autoimmune regulator (AIRE) expression was also demonstrated. Autoimmune complications were seen in 7/12 patients. In two, early transient autoimmune haemolysis settled after treatment and did not recur. The other five suffered ongoing autoimmune problems including: thyroiditis (3); haemolysis (1), thrombocytopaenia (4) and neutropenia (1). Conclusions: This study confirms the previous reports that thymus transplantation can reconstitute T cells in cDGS but with frequent autoimmune complications in survivors

The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen

BACKGROUND: The facultatively anaerobic betaproteobacterium Castellaniella defragrans 65Phen utilizes acyclic, monocyclic and bicyclic monoterpenes as sole carbon source under oxic as well as anoxic conditions. A biotransformation pathway of the acyclic β-myrcene required linalool dehydratase-isomerase as initial enzyme acting on the hydrocarbon. An in-frame deletion mutant did not use myrcene, but was able to grow on monocyclic monoterpenes. The genome sequence and a comparative proteome analysis together with a random transposon mutagenesis were conducted to identify genes involved in the monocyclic monoterpene metabolism. Metabolites accumulating in cultures of transposon and in-frame deletion mutants disclosed the degradation pathway. RESULTS: Castellaniella defragrans 65Phen oxidizes the monocyclic monoterpene limonene at the primary methyl group forming perillyl alcohol. The genome of 3.95 Mb contained a 70 kb genome island coding for over 50 proteins involved in the monoterpene metabolism. This island showed higher homology to genes of another monoterpene-mineralizing betaproteobacterium, Thauera terpenica 58Eu(T), than to genomes of the family Alcaligenaceae, which harbors the genus Castellaniella. A collection of 72 transposon mutants unable to grow on limonene contained 17 inactivated genes, with 46 mutants located in the two genes ctmAB (cyclic terpene metabolism). CtmA and ctmB were annotated as FAD-dependent oxidoreductases and clustered together with ctmE, a 2Fe-2S ferredoxin gene, and ctmF, coding for a NADH:ferredoxin oxidoreductase. Transposon mutants of ctmA, B or E did not grow aerobically or anaerobically on limonene, but on perillyl alcohol. The next steps in the pathway are catalyzed by the geraniol dehydrogenase GeoA and the geranial dehydrogenase GeoB, yielding perillic acid. Two transposon mutants had inactivated genes of the monoterpene ring cleavage (mrc) pathway. 2-Methylcitrate synthase and 2-methylcitrate dehydratase were also essential for the monoterpene metabolism but not for growth on acetate. CONCLUSIONS: The genome of Castellaniella defragrans 65Phen is related to other genomes of Alcaligenaceae, but contains a genomic island with genes of the monoterpene metabolism. Castellaniella defragrans 65Phen degrades limonene via a limonene dehydrogenase and the oxidation of perillyl alcohol. The initial oxidation at the primary methyl group is independent of molecular oxygen

Resonance production in heavy ion collisions

Recent results of resonance production from RHIC at $\sqrt{s_{\rm NN}} =$ 200 GeV and SPS at $\sqrt{s_{\rm NN}} =$ 17 GeV are presented and discussed in terms of the evolution and freeze-out conditions of a hot and dense fireball medium. Yields and spectra are compared with thermal model predictions at chemical freeze-out. Deviations in the low transverse momentum region of the resonance spectrum of the hadronic decay channel, suggest a strongly interaction hadronic phase between chemical and kinetic freeze-out. Microscopic models including resonance rescattering and regeneration are able to describe the trend of the data. The magnitude of the regeneration cross sections for different inverse decay channels are discussed. Model calculations which include elastic hadronic interactions between chemical freeze-out and thermal freeze-out based on the K(892)/K and $\Lambda$(1520)/$\Lambda$ ratios suggest a time between two freeze-outs surfaces of $\Delta \tau>$ 4 fm/c. The difference in momentum distributions and yields for the $\phi$(1020) resonance reconstructed from the leptonic and hadronic decay channels at SPS energy are discussed taking into account the impact of a hadronic phase and possible medium modifications.Comment: 8 pages, 4 figures, conference proceedings (SQM2004