A new sdO+dM binary with extreme eclipses and reflection effect

We report the discovery of a new totally-eclipsing binary (RA=06:40:29.11; Dec=+38:56:52.2; J=2000.0; Rmax=17.2 mag) with an sdO primary and a strongly irradiated red dwarf companion. It has an orbital period of Porb=0.187284394(11) d and an optical eclipse depth in excess of 5 magnitudes. We obtained two low-resolution classification spectra with GTC/OSIRIS and ten medium-resolution spectra with WHT/ISIS to constrain the properties of the binary members. The spectra are dominated by H Balmer and He II absorption lines from the sdO star, and phase-dependent emission lines from the irradiated companion. A combined spectroscopic and light curve analysis implies a hot subdwarf temperature of Teff(spec) = 55 000 +/- 3000K, surface gravity of log g(phot) = 6.2 +/- 0.04 (cgs) and a He abundance of log(nHe/nH) = -2.24 +/- 0.40. The hot sdO star irradiates the red-dwarf companion, heating its substellar point to about 22 500K. Surface parameters for the companion are difficult to constrain from the currently available data: the most remarkable features are the strong H Balmer and C II-III lines in emission. Radial velocity estimates are consistent with the sdO+dM classification. The photometric data do not show any indication of sdO pulsations with amplitudes greater than 7mmag, and Halpha-filter images do not provide evidence of the presence of a planetary nebula associated with the sdO star.Comment: 13 pages, 5 figures; accepted for publication in Ap

CB2 Cannabinoid Receptors Contribute to Bacterial Invasion and Mortality in Polymicrobial Sepsis

BACKGROUND:Sepsis is a major healthcare problem and current estimates suggest that the incidence of sepsis is approximately 750,000 annually. Sepsis is caused by an inability of the immune system to eliminate invading pathogens. It was recently proposed that endogenous mediators produced during sepsis can contribute to the immune dysfunction that is observed in sepsis. Endocannabinoids that are produced excessively in sepsis are potential factors leading to immune dysfunction, because they suppress immune cell function by binding to G-protein-coupled CB(2) receptors on immune cells. Here we examined the role of CB(2) receptors in regulating the host's response to sepsis. METHODS AND FINDINGS:The role of CB(2) receptors was studied by subjecting CB(2) receptor wild-type and knockout mice to bacterial sepsis induced by cecal ligation and puncture. We report that CB(2) receptor inactivation by knockout decreases sepsis-induced mortality, and bacterial translocation into the bloodstream of septic animals. Furthermore, CB(2) receptor inactivation decreases kidney and muscle injury, suppresses splenic nuclear factor (NF)-kappaB activation, and diminishes the production of IL-10, IL-6 and MIP-2. Finally, CB(2) receptor deficiency prevents apoptosis in lymphoid organs and augments the number of CD11b(+) and CD19(+) cells during CLP. CONCLUSIONS:Taken together, our results establish for the first time that CB(2) receptors are important contributors to septic immune dysfunction and mortality, indicating that CB(2) receptors may be therapeutically targeted for the benefit of patients suffering from sepsis

Diosgenin, a Steroidal Saponin, Inhibits Migration and Invasion of Human Prostate Cancer PC-3 Cells by Reducing Matrix Metalloproteinases Expression

BACKGROUND: Diosgenin, a steroidal saponin obtained from fenugreek (Trigonella foenum graecum), was found to exert anti-carcinogenic properties, such as inhibiting proliferation and inducing apoptosis in a variety of tumor cells. However, the effect of diosgenin on cancer metastasis remains unclear. The aim of the study is to examine the effect of diosgenin on migration and invasion in human prostate cancer PC-3 cells. METHODS AND PRINCIPAL FINDINGS: Diosgenin inhibited proliferation of PC-3 cells in a dose-dependent manner. When treated with non-toxic doses of diosgenin, cell migration and invasion were markedly suppressed by in vitro wound healing assay and Boyden chamber invasion assay, respectively. Furthermore, diosgenin reduced the activities of matrix metalloproteinase-2 (MMP-2) and MMP-9 by gelatin zymography assay. The mRNA level of MMP-2, -9, -7 and extracellular inducer of matrix metalloproteinase (EMMPRIN) were also suppressed while tissue inhibitor of metalloproteinase-2 (TIMP-2) was increased by diosgenin. In addition, diosgenin abolished the expression of vascular endothelial growth factor (VEGF) in PC-3 cells and tube formation of endothelial cells. Our immunoblotting assays indicated that diosgenin potently suppressed the phosphorylation of phosphatidylinositide-3 kinase (PI3K), Akt, extracellular signal regulating kinase (ERK) and c-Jun N-terminal kinase (JNK). In addition, diosgenin significantly decreased the nuclear level of nuclear factor kappa B (NF-κB), suggesting that diosgenin inhibited NF-κB activity. CONCLUSION/SIGNIFICANCE: The results suggested that diosgenin inhibited migration and invasion of PC-3 cells by reducing MMPs expression. It also inhibited ERK, JNK and PI3K/Akt signaling pathways as well as NF-κB activity. These findings reveal new therapeutic potential for diosgenin in anti-metastatic therapy

Identification of phytoplasmas on poamceous fruit tree species in Hungary

In Hungary local occurrence of Apple proliferation disease(AP) on apple was described for the first time in the early sixties, since that time the disease has been found in different part of the country based on the results of biological indexing. The first suspicious sign for the presence of Pear decline disease (PD) in Hungarian pear orchard was indicated in the early 70s, but at the time there were no adequate laboratory techniques for identification. The aim of the present study was the molecular identification of phytoplasmas in symptom-showing apple trees, as well as confirmation of the occurrence of PD phytoplasma in symptomatic pear trees, testing them in parallel also on woody indicators. Symptom showing trees, indicating possible phytoplasma infection, were sampled in different growing regions in 2002 for indexing. AP was detected on Golden Delicious using root and double grafting. Typical symptoms of PD did not appear on root or double grafted Pyrus communis cv. Comice. Nucleic acids were prepared from all samples by chloroform/phenol extraction from fresh, frozen or dry phloem tissue of leaves and young branches. Nested PCR procedures were employed with different sets of primers to amplify phytoplasma 16SrDNA, or 16SrDNA plus spacer region. The identity of PCR products was confirmed by RFLP as 16SrX-A (AP) and 16SrX-C (PD). It was concluded that molecular methods were useful for identification of phytoplasmas in several of the symptomatic orchard trees of apple and pear respectively. Both greenhouse indexing and nested PCR/RFLP were suitable for detection and identification of AP from bearing trees and the phytoplasma was identified by molecular methods also in the inoculated AP indicators. PD could not be detected in greenhouse indexing