The Quiescent Cellular State is Arf/p53-Dependent and Associated with H2AX Downregulation and Genome Stability

Cancer is a disease associated with genomic instability and mutations. Excluding some tumors with specific chromosomal translocations, most cancers that develop at an advanced age are characterized by either chromosomal or microsatellite instability. However, it is still unclear how genomic instability and mutations are generated during the process of cellular transformation and how the development of genomic instability contributes to cellular transformation. Recent studies of cellular regulation and tetraploidy development have provided insights into the factors triggering cellular transformation and the regulatory mechanisms that protect chromosomes from genomic instability.     

Characterization of interface defects related to negative-bias temperature instability in ultrathin plasma-nitrided SiON/Si1 0 0 systems

Interface defects related to negative-bias temperature instability (NBTI) in an ultrathin plasma-nitrided SiON/Si1 0 0 system were characterized by using conductance–frequency measurements, electron-spin resonance measurements, and synchrotron radiation X-ray photoelectron spectroscopy. It was confirmed that NBTI is reduced by using D₂-annealing instead of the usual H₂-annealing. Interfacial Si dangling bonds (P_b1 and P_b0 centers) were detected in a sample subjected to negative-bias temperature stress (NBTS). Although we suggest that NBTS also generates non-P_b defects, it does not seem to generate nitrogen dangling bonds. These results show that NBTI of the plasma-nitrided SiON/Si system is predominantly due to P_b depassivation. Plasma nitridation was also found to increase the P_b1/P_b0 density ratio, modify the P_b1 defect structure, and increase the latent interface trap density by generating Si suboxides at the interface. These changes are likely to be the causes of NBTI in ultrathin plasma-nitrided SiON/Si systems.     

Difference in the effectiveness of Ca2+ to evoke catecholamine secretion between adrenaline- and noradrenaline-containing cells of bovine adrenal medulla

Differential adrenaline (Ad) and noradrenaline (NA) secretions evoked by secretagogues were investigated using digitonin-permeabilized adrenal chromaffin cells, cultured adrenal chromaffin cells, and perfused adrenal glands of the ox. In digitonin-permeabilized cells, Ca2+ (0.8-160 microM) caused a concentration-dependent increase in catecholamine secretion, which was characterized by a predominance of NA over Ad secretion. Acetylcholine (10-1,000 microM), high K+ (14-56 mM), and bradykinin (0.1-1,000 nM) all were confirmed to induce the release of more NA than Ad at all concentrations used. There was no apparent difference in the ratios of NA/Ad between Ca(2+)-induced catecholamine secretion from digitonin-permeabilized cells and those induced by secretagogues from cultured cells. Qualitatively the same result was obtained in the secretory responses to acetylcholine and high K+ in perfused adrenal glands. These results indicate that the effectiveness of Ca2+ for catecholamine secretion is higher in the secretory apparatus of NA cells than in that of Ad cells of the bovine adrenal medulla. This may be one of the reasons why the secretagogues cause a predominance of NA secretion over Ad secretion in the bovine adrenal medulla.     

Simultaneous removal of nitrogen oxides and diesel soot particulates catalyzed by perovskite-type oxides

Perovskite-type oxides (ABO₃) catalyzed the simultaneous removal of NO_x and diesel soot particulates in the presence of oxygen, and were superior to transition metal simple oxides in the selectivity for NO_x reduction. Although the catalytic activity of perovskite-type oxides depended on both A-site and B-site cations, the substitution of potassium at A sites prominently promoted the oxidation of soot and the reduction of NO_x.     

Catalytic oxidation of nitrogen monoxide over La1−xCexCoO3 perovskites

This paper presents an investigation on the NO oxidation properties of perovskite oxides. La_1−xCe_xCoO₃ (x = 0, 0.05, 0.1, 0.2, 0.3, 0.4) perovskite-type oxides were synthesized through a citrate method and characterized by XRD, BET and XPS. The catalytic activities were enhanced significantly with Ce substitution, and achieved the best when x was 0.2, but decreased at higher x values. The performed characterizations reveal that the adsorbed oxygen on the surface plays an important role in the oxidation of NO into NO₂. The surface compounds after the co-adsorption of NO and O₂ at room temperature, were investigated by DRIFTS and TPD experiments. Three species: the bridging nitrate, the hyponitrites and the monodentate nitrate, were formed on the surface. The order of thermal stabilities was as follows: monodentate > hyponitrite > bridging. Among them, only the monodentate nitrate which decomposed at above 300 °C, would desorb NO₂ into the gas phase. When Ce was added, the temperature of monodentate nitrate desorption became low and the adsorption of the other two species decreased. This might be related to the oxidation state of Co on the surface. Analysis by synthesizing the characterization results and catalytic activity data shows that large amounts of adsorbed oxygen, small amount of inactive compounds on the surface and low NO₂ desorption temperature are favorable for the oxidation of NO.     

Study on continuous ice slurry formation using functional fluid for ice storage – Discussion of optimal operating conditions

A functional fluid was made by adding a small amount of additive to a water–silicone-oil mixture with 90 vol% water content, and the functional fluid was transformed into an ice slurry by cooling while stirring. The new ice formation system, which authors proposed for ice storage based on the results of previous studies, demonstrated that the ice slurry could be formed continuously for 10 h. In the current paper, experiments were carried out, varying operating conditions, and an optimal operating condition was determined to improve performance of the present system still more. From the experimental results, the conditions necessary to increase the amount of recovery ice were clarified. The time-dependencies of the shape and size of formed ice particles were also shown. Moreover, the reason why the freezing temperature of the functional fluid rose due to repetition of ice formation was clarified, and its measure was discussed. The present study then found that it was possible to form and recover a larger amount of ice than in previous attempts, given the rise in freezing temperature.     

Synthesis, characterization and catalytic activity for NO–CO reaction of Pd–(La, Sr)2MnO4 system

La_xSr_2−xMnO₄ (0 ≤ x ≤ 0.8) oxides were synthesized and single-phase K₂NiF₄-type oxides were obtained in the range of 0.1 ≤ x < 0.5. The catalytic activity of La_xSr_2−xMnO₄ for NO–CO reaction increased with increasing x in the range of solubility limit of La. La_0.5Sr_1.5MnO₄ showed the highest activity among La_xSr_2−xMnO₄ prepared in this study, but its activity was inferior to perovskite-type La_0.5Sr_0.5MnO₃. Among the Pd-loaded catalysts, however, Pd/La_0.8Sr_1.2MnO₄ showed the higher activity and the selectivity to N₂ than Pd/La_0.5Sr_0.5MnO₃ and Pd/γ-Al₂O₃. The excellent catalytic performance of Pd/La_0.2Sr_1.2MnO₄ could be ascribable to the formation of SrPd₃O₄ which was detected by XRD in the catalyst but not in the other two catalysts.