Role of mitochondria in the switch mechanism of the cell death mode from apoptosis to necrosis--studies on rho0 cells

Detailed mechanisms of the switch of the cell death mode from apoptosis to necrosis remain to be solved, although the intracellular level of ATP and that of free radicals have been postulated to be the major factors involved in the mechanisms. In the present study menadione (MEN)-induced cell injury processes were studied using rho0 cells derived from human osteosarcoma 143B cells and parental rho+ cells co-treated with inhibitors of electron transfer chain of mitochondria or oligomycin, an inhibitor of ATP synthesis. Treatment of rho+ cells with 100 microM MEN induced apoptosis, which reached the maximum at 6 h, and was followed by an abrupt decrease thereafter, while necrotic cells (NC) increased continuously when they were judged by Annexin V and PI double staining. On the other hand, MEN induced apoptotic and necrotic changes much faster in rho0 cells compared to rho+ cells. The frequency to find apoptotic cells (AP) in the former cells was distinctly smaller than that to find NC judged by Annexin V and PI double staining. Electron microscopically, a major population of rho0 cells treated with MEN for 6 h consisted of intermediate cells, and a small number of AP co-existed. At 9 h of the treatment intermediate cells were exclusively seen, and AP were hardly detected. When parental rho+ cells were treated with MEN in the presence of oligomycin or oligomycin plus antimycin A both apoptotic and necrotic changes of the cells were distinctly accelerated. The intracellular level of superoxide in rho0 cells continuously increased after the MEN treatment, whereas that of ATP remained distinctly low before and after the MEN treatment compared to that in rho+ cells. These data suggest that the intracellular level of superoxide may be a key factor controlling the switch from apoptosis to necrosis.     

GPC Profile Change of Potato Starch with Extrusion Processing

Native potato starch (moisture content 15%) was treated by twin screw extruder under four operating conditions with varying barrel temperatures (110°C–230°C). These modified starch samples were compared to native and drum-dried starch. Starch sample solution for gel chromatography was prepared by the three methods (acidic, alkaline, and neutral methods). They were subjected to gel chromatography on Toyopearl HW-75, and some difference was found among the three gel chromatographic patterns obtained from the same starch solution. This discrepancy among GPC patterns suggests formation of some types of anhydro-bonds between chains of amylopectin and or amylose in the extrusion process. Elevating barrel temperature increases degree of depolymerization. The size of fragments formed with the treatment is bigger than that of oligosaccharides but smaller than that of amylose.     

High-Speed TDM–WDM Techniques for Long-Haul Submarine Optical Amplifier Systems

Optical amplifier techniques have led to the installation of large-capacity submarine systems and further capacity increases seem likely. This paper reviews the FSA submarine system, which flexibly operates at both 2.5 and 10 Gb/s and offers maximum transmission capacity of 60 Gb/s for commercial use. The system configuration as well as its characteristics and upgradability will be introduced, including measurement results on time-division-multiplexing/wavelength-division-multiplexing (TDM–WDM) transmission at bit rates of 10 and 20 Gb/s using non-return-to-zero or soliton pulses. To further increase transmission capacity, TDM–WDM techniques that permit more than 10 Gb/s signal transmission in each data channel should be developed. Thus, pulse formats, which include non-return-to-zero, return-to-zero, or soliton pulses, and dispersion allocation in transmission fibers are significant issues. We introduce and discuss our recent results from high-speed (10 to 40 Gb/s) TDM–WDM signal transmission experiments with regard to the above aspects.     

Design and performance evaluation of amplifier modules in stackable ROADMs for low-cost CWDM access networks

Coarse wavelength division multiplexing (CWDM) network has proven to be promising lower cost network architecture for a significant cost advantage over dense wavelength division multiplexing due to the lower cost of lasers and the filters used in CWDM modules. A compatible amplifier module having bidirectional amplification capability was deployed for introducing inside stackable reconfigurable optical add/drop multiplexers in realizing large-scale CWDM networks. The amplifier module for use in the bidirectional IP transmission confirmed that the insertion losses of the nodes and the losses of the fibers connecting the nodes can be compensated effectively, allowing the network administrator to increase the number of nodes and fiber length of the network. However, the noise generated from the amplification due to amplified spontaneous emission must be considered in network design issues. In this paper, optical power penalties due to the bidirectional amplification were estimated by conducting experimentation on minimum detectable power of optical transceivers. After analyzing the power penalty issue, an IP-over-CWDM ring network was implemented and the performance of network was evaluated by monitoring the power and packet transmissions before and after the amplifier module was turned on.     

Synthesis of Nanohole‐Structured Single‐Crystalline Platinum Nanosheets Using Surfactant‐Liquid‐Crystals and their Electrochemical Characterization

Nanohole‐structured single‐crystalline Pt nanosheets have been synthesized by the borohydride reduction of Na₂PtCl₆ confined to the lyotropic liquid crystals (LLCs) of polyoxyethylene (20) sorbitan monooleate (Tween 80) with or without nonaethylene‐glycol (C₁₂EO₉). The Pt nanosheets of around 4–10 nm in central thickness and up to 500 nm or above in diameter have a number of hexagonal‐shaped nanoholes ∼1.8 nm wide. High‐resolution electron microscope images of the nanosheets showed atomic fringes with a spacing of 0.22 nm indicating that the nanosheets are crystallographically continuous through the nanoholed and non‐holed areas. The inner‐angle distributions for the hexagonal nanoholes indicate that the six sides of the nanoholes are walled with each two Pt (111), Pt (1 1) and Pt (010) planes. The formation mechanism of nanoholed Pt nanosheets is discussed on the basis of structural and compositional data for the resulting solids and their precursory LLCs, with the aid of similar nanohole growth observed for a Tween 80 free but oleic acid‐incorporated system. It is also demonstrated that the nanoholed Pt nanostructures loaded on carbon exhibit fairly high electrocatalytic activity for oxygen reduction reaction and a high performance as a cathode material for polymer‐electrolyte fuel cells, along with their extremely high thermostability revealed through the effect of electron‐irradiation.     

Selective sorption of heavy metal thiocyanate complexes on crown ether resin

The sorption behavior of heavy metal thiocyanate complexes was investigated for dibenzo-18-crown-6 (DB18C6) resin and bis[2-(o-methoxyphenoxy)ethyl]ether (BMPE) resin. The DB18C6 resin showed a high sorption ability and the degree of zinc sorption increased significantly with thiocyanate concentration. This behavior was not observed for BMPE resin. The sorption behavior was influenced by the countercation species, and the degree of sorption of zinc ions showed the maximum when the potassium thiocyanate was used as a complexing salt. The sorbed species appear to be KZn(SCN)₃, K₂Zn(SCN)₄ in the potassium thiocyanate system, and Zn(SCN)₂ in the lithium thiocyanate system, respectively, according to analysis of the sorption equilibrium. Sodium and ammonium thiocyanate systems show an intermediate behavior of the two. The sorption selectivity for DB18C6 resin depended not only on the hydrophobic nature of heavy metal thiocyanate complexes but also on the stabilization of counter cation species with crown ether matrix, and the sorption selectively was found to be effectively controlled by countercation species according to the cation-chelation mechanism.     

ArF excimer laser induced CVD of aluminum oxide films

The authors have demonstrated photochemical deposition of aluminum oxides from Trimethylaluminum (TMA) and N₂O by using a pulsed ArF excimer laser (193 nm). Both TMA and N₂O are efficiently photodissociated by the 193 nm light. The films are grown on Si and InP wafers contained in a low pressure flowing cell with a heated substrate. The incident laser beam is focused and parallel to the substrate surface. Typical deposition rates are 80–150 A/min. Stripes of aluminum oxide 30 mm wide are uniformly grown on 7.5 cm Si-wafers. The film composition and purity have been investigated using Auger and Infra-red spectroscopy analysis. Surprising results are the relatively low concentration of carbon. Refractive index and thickness have been determined by an ellipsometer. Typical values for the films are 1.54–1.62. Metal-oxide-semiconductor capacitors have been fabricated and characterized. The C-V curves for n-InP/aluminum oxide have clockwise hysteresis, and minimum loop width is less than 0.5 V. The surface state densities are 1 × 10¹¹ cm^-2 eV⁻¹ at the mid band gap.     

PTCR Characteristics in Barium Titanate Ceramics with Curie Points Between 60° and 360°C

PTCR characteristics in porous semiconducting barium titanate ceramics with Curie points from 60° to 360°C were investigated. The magnitude of the PTCR effect in these cerumics decreases self-onsistently with increasing Curie point within this temperature range. A PTCR efSect of more than 4 orders of magnitude was ahserved, for a Ba_0.44Pb_0.6TiO₃ ceramic with a Curie point of 360°C .