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Sufficient Amounts (sufficient + amount)
Selected AbstractsResource allocation for statistical quality of service provision in buffered crossbar switches,INTERNATIONAL JOURNAL OF COMMUNICATION SYSTEMS, Issue 6 2008Qiang Duan Abstract The buffered crossbar switch is a promising switching architecture that plays a crucial role for providing quality of service (QoS) in computer networks. Sufficient amount of resources,bandwidth and buffer space,must be allocated in buffered crossbar switches for QoS provision. Resource allocation based on deterministic QoS objectives might be too conservative in practical network operations. To improve resource utilization in buffered crossbar switches, we study the problem of resource allocation for statistical QoS provision in this paper. First, we develop a model and techniques for analyzing the probabilistic delay performance of buffered crossbar switches, which is described by the delay upper bound with a prescribed violation probability. Then, we determine the required amounts of bandwidth and buffer space to achieve the probabilistic delay objectives for different traffic classes in buffered crossbar switches. In our analysis, we apply the effective arrival envelope to specify traffic load in a statistical manner and characterize switch service capacity by using the service curve technique. Instead of just focusing on one specific type of scheduler, the model and techniques developed in this paper are very flexible and can be used for analyzing buffered crossbar switches with a wide variety of scheduling algorithms. Copyright © 2007 John Wiley & Sons, Ltd. [source] HCV-RNA In Sural Nerve From Hcv Infected Patients With Peripheral NeuropathyJOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, Issue 1 2001L De Martino Objective: Evaluation of hepatitis C virus (HCV) by reverse transcription-polymerase chain reaction (RT-PCR) in peripheral nerve tissues from HCV infected patients with peripheral neuropathy. METHODS: RT-PCR was performed on homogenates of nerve biopsies from 17 consecutive HCV-positive patients with peripheral neuropathy, with or without mixed cryoglobulinemia, hospitalised from 1996 to 2000. Sural nerve specimens were frozen in iso-pentane pre-cooled in liquid nitrogen and stored at ,80°C until use. RNA was extracted from ten 7-,m thick cryostatic sections or from a nerve trunk specimen of about 3 mm length, collected from each biopsy. Three different protocols of RNA extraction were tested (1,3). Complementary DNAs (cDNAs) were obtained without or with RNasin (Promega, Madison, WI) addition in the reaction mixture to inhibit residual RNase activity. Two sets of commercially available PCR primers for the outer and the nested reaction were used. PCR products were analysed by agarose gel electrophoresis and ethidium bromide staining. Serum samples and liver specimens from proven HCV positive patients served as positive controls, whereas sera from healthy subjects were negative controls. RESULTS: Sufficient amount of RNA could be obtained either by cryostatic sections or by in toto nerve specimens. Extraction by Trizol (Gibco-BRL) allowed the best concentration and purity of RNA as assessed by biophotometry. The presence of RNasin didn't improve the cDNA synthesis. The resulting amplification product of the nested PCR was 187 bp long. We have always observed this product in our positive controls and never in the negative. Six samples from patients either with or without cryoglobulinemia resulted positive; 7 were negative. Four samples gave variable results. CONCLUSIONS: While 40% of the nerves in our series were undoubtedly HCV positive, the cause(s) of negative and variable results in the remaining samples is likely more complex than variations in the detection protocols and deserve further investigations. REFERENCES: 1) Chomczynski P, Sacchi N (1987). Anal Biochem 162:156. 2) Marquardt O et al. (1996). Med Microbiol Lett 5:55. 3) Chomczynski P (1993). Bio/Techniques 15:532. [source] Determination of the operational pH value of a buffering membrane by an isoelectric trapping separation of a carrier ampholyte mixtureELECTROPHORESIS, Issue 5 2008Robert Y. North Abstract The operational pH value of a buffering membrane used in an isoelectric trapping separation is determined by installing the membrane as the separation membrane into a multicompartmental electrolyzer operated in the two-separation compartment configuration. A 3 What Is an Asset Price Bubble?EUROPEAN FINANCIAL MANAGEMENT, Issue 1 2003An Operational Definition This paper reviews and analyses the current definitions of bubbles in asset prices. It makes the case that one cannot identify a bubble immediately, but one has to wait a sufficient amount of time to determine whether the previous prices can be justified by subsequent cash flows. The paper proposes an operational definition of a bubble as any time the realised asset return over given future period is more than two standard deviations from its expected return. Using this framework, the paper shows how the great crash of 1929 and 1987,both periods generally characterised as bubbles,prove not to be bubbles but the low point in stock prices in 1932 is a ,negative bubble.' The paper then extends this analysis to the internet stocks and concludes that it is virtually certain that it is a bubble. [source] Fruit and fibre: the nutritional value of figs for a small tropical ruminant, the blue duiker (Cephalophus monticola)AFRICAN JOURNAL OF ECOLOGY, Issue 4 2009Erin L. Kendrick Abstract Tropical forests throughout the world are home to a guild of small ruminants that consume fruit as a substantial portion of their diet. Because the rumen is relatively inefficient at digesting nonstructural carbohydrates and only slowly digests cellulose, the feeding adaptations of frugivorous ruminants are enigmatic. We examined the nutritional value of wild figs to blue duikers, one of the smallest and most frugivorous ruminants, through chemical analyses and a series of digestion trials with six species of wild African figs. These figs were high in fat, protein, cell wall, lignin and Ca : P ratios, low in sugar and starch, and high in unextractable, fibre-bound tannins when compared with many other fruits. The fibre-bound tannins and protein caused protein digestibility and nitrogen balance to be consistently low or negative. The high fibre content of the figs allowed duikers to only digest 30,60% of energy contained in the figs. However, duikers were able to consume enough digestible energy to maintain body mass during 4-day trials. Therefore, a ruminant digestive system is beneficial to mammals eating high fibre, high-tannin tropical fruit like figs, especially if the mammal is small enough to harvest a sufficient amount to meet its daily energy requirements and has adaptations for reducing the effects of tannins on protein digestibility. Résumé Les forêts tropicales du monde entier abritent toute une faune de petits ruminants dont les fruits constituent une part non négligeable de l'alimentation. Comme le rumen est relativement peu efficace pour digérer les hydrates de carbone non structuraux et ne digère que lentement la cellulose, les adaptations alimentaires des ruminants frugivores sont encore énigmatiques. Nous avons examiné la valeur nutritionnelle des figues sauvages pour le céphalophe bleu, un des ruminants les plus petits et parmi les plus frugivores, au moyen d'analyses chimiques et d'une série d'essais de digestion avec six espèces de figues sauvages africaines. Ces figues étaient riches en graisses, en protéines, en parois cellulaires, en lignine, et leur rapport Ca/P était élevé; elles avaient un contenu faible en sucre et en amidon, et beaucoup de tanins impossibles à extraire, liés aux fibres, comparés à de nombreux autres fruits. Les tanins liés aux fibres et les protéines faisaient que la digestibilité des protéines et l'équilibre azotéétaient en permanence faibles ou négatifs. Le contenu en fibres élevé des figues ne permettait aux céphalophes de digérer que 30 à 60% de l'énergie contenue dans les figues. Cependant, pendant les quatre jours du test, les céphalophes ont pu consommer suffisamment d'énergie digestible pour conserver leur masse corporelle. C'est pourquoi le système digestif des ruminants est bénéfique pour les mammifères qui consomment des fruits tropicaux riches en fibres et en tanins, comme les figues, spécialement si le mammifère est assez petit pour pouvoir en trouver une quantité suffisante pour répondre à ses besoins quotidiens en énergie, et qu'il possède des adaptations qui lui permettent de réduire les effets des tanins sur la digestibilité des protéines. [source] Sintering Characteristics in the BaTiO3,Nb2O5,Co3O4 Ternary System: II, Stability of So-called "Core,Shell" StructureJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2000Hirokazu Chazono The sintering characteristics and the reaction of additives with BaTiO3 (BT) were examined for two materials having Nb-rich composition (Comp.N) and Co-rich composition (Comp.C) to elucidate the relation between the stability of the core,shell microstructure and the Nb/Co ratio in the BT,Nb2O5,Co3O4 system. TEM observation revealed that the concentration gradient of Nb and Co existed in the shell region although Nb and Co macroscopically distributed homogeneously. X-ray diffraction analysis showed that the shell formation preceded the densification and completed at about 1280°C for both Comp.N and Comp.C as determined from differential scanning calorimetry. A diffusion couple experiment disclosed that Co had a larger diffusivity than Nb and that the diffusion of Co was suppressed when the sample was codoped with a sufficient amount of Nb. On the basis of these experimental results, new mechanisms of the formation and collapse of core,shell structure in the BT,Nb2O5,Co3O4 system were proposed. [source] How many symbionts are provided by mothers, acquired by offspring, and needed for successful vertical transmission in an obligate insect,bacterium mutualism?MOLECULAR ECOLOGY, Issue 24 2007TAKAHIRO HOSOKAWA Abstract Vertical symbiont transmission is among the most pivotal processes for maintenance of symbiotic associations. However, it is poorly understood whether and how the levels of resource allocation and investment upon vertical transmission are regulated. The stinkbug Megacopta punctatissima is obligatorily associated with the gut symbiotic bacterium ,Candidatus Ishikawaella capsulata', whose transmission is mediated by a unique mechanism called ,symbiont capsule'. We investigated the population dynamics of the symbiont during vertical transmission in the host,symbiont mutualism. The stinkbug mothers produced one capsule for around 3.6 eggs irrespective of clutch size, suggesting a strict maternal control over symbiont supply for the offspring. However, experimental manipulation of egg/capsule ratios revealed that one capsule is sufficient for symbiont transmission to six nymphs. Quantitative polymerase chain reaction analyses demonstrated that a capsule contains 1.2 × 108 symbionts, a newborn nymph possesses 2 × 107 symbionts from a capsule, and thus one capsule certainly contains a sufficient amount of symbiont cells for six nymphs. These results indicated that the stinkbug mothers produce 1.7 times more symbiont capsules than needed. The newborn nymphs consistently harboured around 2 × 107 symbionts, also suggesting a nymphal control over symbiont transmission. The threshold symbiont titre minimally needed for successful vertical transmission was estimated to be 1.9 × 106 symbionts, which is only 1/10 of the actual symbiont titre detected in a newborn nymph. These results illuminate several ecological factors that may be relevant to parental and offspring controls over symbiotic resource allocation through host insect generations. [source] Comparative 1H NMR studies of saturation transfer in copolymer gels and mouse lensesNMR IN BIOMEDICINE, Issue 6 2010Koji Nakamura Abstract Saturation transfer in cross-linked copolymer gels and excised intact and perforating trauma-induced cataract mouse lenses (4- or 8-week-old) were studied using intermolecular cross-relaxation rates (1/TIS(H2O); 1/TIS), monitored with f2 -irradiation at ,8.79, ,4.00, and 7.13,ppm (,H2/2,,,,69,Hz). [1] The 1/TIS(7.13,ppm) vs dry weight [W (%)] profiles for hydrophilic copolymer gels were far steeper than those for hydrophobic copolymer gels, indicating the participation of an amount of bound water and a number of copolymer hydroxyl groups in the saturation transfer process. In contrast, the 1/TIS(,8.79,ppm) vs W (%) profiles exhibited little difference between the hydrophilic and hydrophobic copolymer gels, indicating the major participation of molecular rigidity, i.e. W (%) in the saturation transfer process. [2] The 1/TIS(7.13,ppm) values for cataractous mouse lenses were larger than those for intact lenses, indicating the formation of large, immobile lens protein associates or aggregates containing a sufficient amount of bound water for the saturation transfer. [3] The 1/TIS(7.13,ppm) vs W (%) profiles for the hydrophilic copolymer gels exhibited similar characteristics to the intact and cataractous mouse lenses with regard to the saturation transfer process. Copyright © 2010 John Wiley & Sons, Ltd. [source] Development and calibration of a nitrification PDE model based on experimental data issued from biofilter treating drinking waterBIOTECHNOLOGY & BIOENGINEERING, Issue 2 2006I. Queinnec Abstract To remove ammonia for production of drinking water, nitrification can be performed in a bio-filter. At least 1 month is necessary to capture from the groundwater and then grow a sufficient amount of nitrifying bacteria to reach the desired removal efficiency. Improving start-up of bio-filters at low substrate concentration is therefore a major challenge. In this connection, it is important to develop appropriate models for designing, monitoring or analysing biofilm systems during start-up or following disinfection events. This study discusses the development and calibration of a nitrification PDE model which reflects the compromise between the complexity associated with the description of the full physical and biochemical mechanisms and the search for a simplified model with identifiable parameters. This model takes only the relevant phenomena (considering the full operating range) into account. The validity of the calibrated model has been evaluated through experiments under very different operational conditions, at the laboratory and under real industrial conditions, involving the full upstream chain of water treatment (iron oxidation and sand filter). © 2006 Wiley Periodicals, Inc. [source] Novel microfluidic platform for culturing neurons: Culturing and biochemical analysis of neuronal componentsBIOTECHNOLOGY JOURNAL, Issue 11 2009Jeong Won Park Abstract Neurons, one of the most polarized types of cells, are typically composed of cell bodies (soma), dendrites, and axons. Many events such as electric signal transmission, axonal transport, and local protein synthesis occur in the axon, so that a method for isolating axons from somata and dendrites is required for systematically investigating these axonal events. Based on a previously developed neuron culture method for isolating and directing the growth of central nervous system axons without introducing neutrophins, we report three modified microfluidic platforms: (1) for performing biochemical analysis of the pure axonal fraction, (2) for culturing tissue explants, and (3) a design that allows high content assay on same group of cells. The key feature of these newly developed platforms is that the devices incorporate a number of microgrooves for isolating axons from the cell body. They utilize an open cellculture area, unlike the enclosed channels of the previous design. This design has extended the axonal channel so that a sufficient amount of pure axonal fraction can be obtained to perform biochemical analysis. The design also addresses the drawback of the previous neuron culture device, which was not adaptable for culturing thick neuronal tissues such as brain explants, neurospheres, and embryoid bodies, which are essential model tissues in neuroscience research. The design has an open cellculture area in the center and four enclosed channels around open area, and is suitable for multiple drug screening assays. [source] Tumor hypoxia: A target for selective cancer therapyCANCER SCIENCE, Issue 12 2003Shinae Kizaka-Kondoh Tumor hypoxia has been considered to be a potential therapeutic problem because it renders solid tumors more resistant to sparsely ionizing radiation (IR) and chemotherapeutic drugs. Moreover, recent laboratory and clinical data have shown that tumor hypoxia is also associated with a more malignant phenotype and poor survival in patients suffering from various solid tumors. Therefore, selective targeting of hypoxic tumor cells has been explored, and since severe hypoxia (pO2<0.33%, 2.5 mmHg) does not occur in normal tissue, tumor hypoxia could be exploited for therapeutic advantage. However, the following three characteristics of hypoxic tumor regions present obstacles in targeting hypoxic cells. First, it is difficult to deliver a sufficient amount of drug to a region that is remote from blood vessels. Second, one must specifically target hypoxic tumor cells while sparing normal well-oxygenated tissue from damage. Finally, the severely hypoxic tumor cells to be attacked have often stopped dividing. Therefore, high delivery efficiency, high specificity and selective cytotoxicity are all necessary to target and combat hypoxic tumor cells. The current review describes progress on the biological aspects of tumor hypoxia and provides a compilation of the recent molecular approaches used to target hypoxic tumors. These approaches include our work with a unique hypoxia-targeting protein drug, TOP3, with which we have sought to address the above three difficulties. [source] Preparation of Core,Shell-Structured Nanoparticles (with a Noble-Metal or Metal Oxide Core and a Chromia Shell) and Their Application in Water Splitting by Means of Visible LightCHEMISTRY - A EUROPEAN JOURNAL, Issue 26 2010Kazuhiko Maeda Dr. Abstract Core,shell-structured nanoparticles, consisting of a noble metal or metal oxide core and a chromia (Cr2O3) shell, were studied as promoters for photocatalytic water splitting under visible light. Core nanoparticles were loaded by impregnation, adsorption or photodeposition onto a solid solution of gallium nitride and zinc oxide (abbreviated GaN:ZnO), which is a particulate semiconductor photocatalyst with a band gap of approximately 2.7,eV, and a Cr2O3 shell was formed by photodeposition using a K2CrO4 precursor. Photodeposition of Cr2O3 on GaN:ZnO modified with a noble metal (Rh, Pd and Pt) or metal oxide (NiOx, RuO2 and Rh2O3) co-catalyst resulted in enhanced photocatalytic activity for overall water splitting under visible light (,>400,nm). This enhancement in activity was primarily due to the suppression of undesirable reverse reactions (H2,O2 recombination and/or O2 photoreduction) and/or protection of the core component from chemical corrosion, depending on the core type. Among the core materials examined, Rh species exhibited relatively high performance for this application. The activity for visible-light water splitting on GaN:ZnO modified with an Rh/Cr2O3 core,shell configuration was dependent on both the dispersion of Rh nanoparticles and the valence state. In addition, the morphology of the Cr2O3 photodeposits was significantly affected by the valence state of Rh and the pH at which the photoreduction of K2CrO4 was conducted. When a sufficient amount of K2CrO4 was used as the precursor and the solution pH ranged from 3 to 7.5, Cr2O3 was successfully formed with a constant shell thickness (,2,nm) on metallic Rh nanoparticles, which resulted in an effective promoter for overall water splitting. [source] Amplification of low quantity bacterial RNA for microarray studies: time-course analysis of Leptospirillum ferrooxidans under nitrogen-fixing conditions,ENVIRONMENTAL MICROBIOLOGY, Issue 6 2006Mercedes Moreno-Paz Summary We have developed a method for the amplification of low quantity total bacterial RNA for DNA microarrays analysis. Current methods are based on the linear amplification by the in vitro transcription from the T7 promoter, similar to that used for eukaryotic mRNA amplification. For the incorporation of T7 promoter, the prokaryotic RNA must be enzymatically modified for the incorporation of a polyA tail at the 3, end to emulate the eukaryotic mRNA. The method we describe and validate herein avoids this step by the direct and random incorporation of the T7 promoter. From 500 ng of total bacterial RNA, we obtained 130,150 µg of antisense RNA, such products being good substrate for fluorescent labelling and DNA microarray analysis. The method was validated with bacterial samples from which it is very difficult to obtain sufficient amounts and quality of total RNA for global gene expression analysis. This is critical for low cell density growing microorganisms, environmental samples, or many extremophiles where the composition of the cultural media severely affects the RNA yield, like in the case of the acidophile and iron oxidizer Gram-negative bacterium Leptospirillum ferrooxidans. We further validated our amplification method in parallel experiments with non-amplified RNA by following the expression of the L. ferrooxidans nif regulon along the time-course of growth. [source] Freeze-and-thaw-disrupted tumour cells impair the responsiveness of DC to TLR stimulationEUROPEAN JOURNAL OF IMMUNOLOGY, Issue 10 2008Iñigo Tirapu Abstract Cancer immunotherapy aims at inducing immune responses against tumour-associated antigens that mediate the eradication of tumour cells. For successful vaccination against antigens expressed by the tumour, the immune system has to be provided with sufficient amounts of these antigens in connection with strong immunostimulatory signals such as toll-like receptor (TLR) ligands. Tumour cells represent a convenient source of relevant tumour-associated antigens but can have suppressive properties. In this study, we explored how different forms of tumour cell material influence the activation of dendritic cells (DC), which play a crucial role in the induction of anti-tumour immune responses. We show that freeze-and-thaw-disrupted tumour cells inhibit DC activation in response to TLR stimulation, a phenomenon that is only partially seen with non-disrupted control cells. This suppression of DC stimulation is independent of tumour cell- and species-specific factors. We tested the hypothesis that phosphatidylserine on cells with disrupted membrane integrity mediates inhibition of TLR-induced DC activation. Our experimental evidence indicates that phosphatidylserine is not involved in the inhibition of TLR-mediated DC activation by freeze-and-thaw-disrupted cells. The inhibitory activity associated with disrupted tumour cells could explain why such preparations are less effective tumour vaccines than apoptotic tumour cells. [source] A JÖKULHLAUP FROM A LAURENTIAN CAPTURED ICE SHELF TO THE GULF OF MEXICO COULD HAVE CAUSED THE BØLLING WARMINGGEOGRAFISKA ANNALER SERIES A: PHYSICAL GEOGRAPHY, Issue 2 2008ULF ERLINGSSON ABSTRACT. Since the rapid rate of global warming at the onset of the Bølling interstadial became evident, its cause has been under debate. It coincides closely in time with a strong global transgression called meltwater pulse 1a. One attempt at solution says that a meltwater pulse of Antarctic origin could cause an increase in North Atlantic Deep Water formation, and thus give rise to the Bølling interstadial. However, others have disputed that Antarctic meltwater would have that effect, and furthermore, the start of the Bølling interstadial is not even associated with an increase in North Atlantic Deep Water. A controversial hypothesis says that some Laurentian meltwater came from a jökulhlaup (sub-glacial outburst flood), but no study has yet shown unequivocally that sufficient amounts of water could be stored under the ice. Furthermore, according to all available data a melt-water pulse from the Laurentian ice would give rise to strong cooling, not warming. Nevertheless, meg-afloods appear instrumental in accumulating the Mississippi Fan, created entirely during the Quaternary period, and dramatic climate changes are characteristic of this period. This paper presents a hypothetical chain of events, building on the published literature and simple calculations, to investigate whether the order of magnitude is reasonable. The hypothesis is that a jökulhlaup from a Laurentian captured ice shelf flowed out through the Mississippi, boosted the Gulf Stream, reinvigorated the North Atlantic circulation, and as a result triggered the Bølling warm phase. [source] Collection of peripheral blood stem cells with granulocyte-colony-stimulating factor alone in testicular cancer patientsINTERNATIONAL JOURNAL OF UROLOGY, Issue 3 2000KISABURO HANAZAWA Abstract Background: High-dose chemotherapy with the transplantation of peripheral blood stem cells (PBSC) has been performed for the treatment of advanced testicular cancer patients. Recently, it has been reported that, in healthy donors, a large quantity of stem cells can be transferred to peripheral blood using granulocyte-colony-stimulating factor (G-CSF) alone. Therefore, it was decided to try to harvest PBSC from three patients having testicular cancers with G-CSF alone. Methods: The three patients with testicular cancer were 26, 56 and 62-years-old. They had undergone five, two and three cycles of chemotherapy, respectively, but no radiation therapy. Granulocyte colony-stimulating factor was subcutaneously injected (250 ,g) into each patient twice per day for 6 days. Peripheral blood stem cells were harvested for 3 days (days 4,6) and mononuclear cells (MNC), CD34-positive cells and colony-forming units of granulocyte-macrophage (CFU-GM) in PBSC collected by apheresis were measured. Results: Apheresis showed that the total MNC count was 20.2 × 108/kg (range, 10.6,25.9 × 108/kg), the CD34-positive cell count was 0.98 × 106/kg (range, 0.75,1.4 × 106/kg) and the total CFU-GM count was 1.36 × 105/kg (range, 0.25,3.0 × 105/kg). Conclusion: After mobilization of peripheral blood stem cells with G-CSF alone, sufficient amounts of MNC were obtained from testicular cancer patients who had undergone chemotherapy several times. However, sufficient amounts of CD34-positive cells and CFU-GM could not be obtained. These results suggested that the G-CSF dose was not adequate for harvesting sufficient amounts of CD34-positive cells and CFU-GM. [source] Cold-adapted signal proteins: NMR structures of pheromones from the antarctic ciliate Euplotes nobiliiIUBMB LIFE, Issue 8-9 2007William J. Placzek Abstract Cell type-specific signal proteins, known as pheromones, are synthesized by ciliated protozoa in association with their self/nonself mating-type systems, and are utilized to control the vegetative growth and mating stages of their life cycle. In species of the most ubiquitous ciliate, Euplotes, these pheromones form families of structurally homologous molecules, which are constitutively secreted into the extracellular environment, from where they can be isolated in sufficient amounts for chemical characterization. This paper describes the NMR structures of En-1 and En-2, which are members of the cold-adapted pheromone family produced by Euplotes nobilii, a species inhabiting the freezing coastal waters of Antarctica. The structures were determined with the proteins from the natural source, using homonuclear 1H NMR techniques in combination with automated NOESY peak picking and NOE assignment. En-1 and En-2 have highly homologous global folds, which consist of a central three-,-helix bundle with an up-down-up topology and a 310-helical turn near the N-terminus. This fold is stabilized by four disulfide bonds and the helices are connected by bulging loops. Apparent structural specificity resides in the variable C-terminal regions of the pheromones. The NMR structures of En-1 and En-2 provide novel insights into the cold-adaptive modifications that distinguish the E. nobilii pheromone family from the closely related E. raikovi pheromone family isolated from temperate waters. [source] Oligonucleotide probes for specific detection of Giardia lamblia cysts by fluorescent in situ hybridizationJOURNAL OF APPLIED MICROBIOLOGY, Issue 5 2001M.R. Dorsch Aims:,Our study focused on the design of oligonucleotide probes and a suitable hybridization protocol that would allow rapid and specific identification of potentially viable cysts of the waterborne parasite Giardia lamblia. Methods and Results:,Comparative analysis of ribosomal RNA (rRNA) sequences of Giardia lamblia and a number of closely and more distantly related species identified six regions that appear to be specific for the G. lamblia 16S rRNA. Fluorescently labelled probes targeting these regions were produced and employed in fluorescent in situ hybridization (FISH) experiments. Two of the six probes tested successfully. Conclusions:,Our study provides the first reported probes for specific FISH detection of G. lamblia. The method depends on sufficient amounts of intact rRNA in the target organism, which is unlikely to be present in nonviable cysts that have been exposed to the environment for a prolonged period. Significance and Impact of the Study:,Currently, detection of G. lamblia cysts is largely based on immunofluorescence assays (IFA) targeting cyst wall surface antigens. These assays lack specificity and will detect species others than G. lamblia. Further, IFA will detect nonviable cysts and cyst wall fragments that do not pose a public health risk. In contrast, FISH probes allow specific detection and are likely to only detect viable, infectious cysts. [source] Vitamin D Hormone Inhibits Osteoclastogenesis In Vivo by Decreasing the Pool of Osteoclast Precursors in Bone MarrowJOURNAL OF BONE AND MINERAL RESEARCH, Issue 4 2002Takeshi Shibata Abstract Previous observations that vitamin D hormone induces the expression of the receptor activator of nuclear factor ,B (NF-,B) ligand (RANKL), thereby stimulating osteoclastogenesis in vitro, led to the widespread belief that 1,,25-dihydroxyvitamin D3 [1,,25(OH)2D3] is a bone-resorbing hormone. Here, we show that alfacalcidol, a prodrug metabolized to 1,,25(OH)2D3, suppresses bone resorption at pharmacologic doses that maintain normocalcemia in an ovariectomized (OVX) mouse model of osteoporosis. Treatment of OVX mice with pharmacologic doses of alfacalcidol does not increase RANKL expression, whereas toxic doses that cause hypercalcemia markedly reduce the expression of RANKL. When bone marrow (BM) cells from OVX mice were cultured with sufficient amounts of macrophage colony-stimulating factor (M-CSF) and RANKL, osteoclastogenic activity was higher than in sham mice. Marrow cultures from alfacalcidol- or estrogen-treated OVX mice showed significantly less osteoclastogenic potential compared with those from vehicle-treated OVX mice, suggesting that the pool of osteoclast progenitors in the marrow of vitamin D-treated mice as well as estrogen-treated mice was decreased. Frequency analysis showed that the number of osteoclast progenitors in bone marrow was increased by OVX and decreased by in vivo treatment with alfacalcidol or estrogen. We conclude that the pharmacologic action of active vitamin D in vivo is to decrease the pool of osteoclast progenitors in BM, thereby inhibiting bone resorption. Because of its unusual activity of maintaining bone formation while suppressing bone resorption, in contrast to estrogens that depress both processes, vitamin D hormone and its bone-selective analogs may be useful for the management of osteoporosis. [source] Spatial insulin signalling in isolated skeletal muscle preparationsJOURNAL OF CELLULAR BIOCHEMISTRY, Issue 5 2010Peter Sogaard Abstract During in vitro incubation in the absence or presence of insulin, glycogen depletion occurs in the inner core of the muscle specimen, concomitant with increased staining of hypoxia-induced-factor-1-alpha and caspase-3, markers of hypoxia and apoptosis, respectively. The aim of this study was to determine whether insulin is able to diffuse across the entire muscle specimen in sufficient amounts to activate signalling cascades to promote glucose uptake and glycogenesis within isolated mouse skeletal muscle. Phosphoprotein multiplex assay on lysates from muscle preparation was performed to detect phosphorylation of insulin-receptor on Tyr1146, Akt on Ser473 and glycogen-synthases-kinase-3 on Ser21/Ser9. To address the spatial resolution of insulin signalling, immunohistochemistry studies on cryosections were performed. Our results provide evidence to suggest that during the in vitro incubation, insulin sufficiently diffuses into the centre of tubular mouse muscles to promote phosphorylation of these signalling events. Interestingly, increased insulin signalling was observed in the core of the incubated muscle specimens, correlating with the location of oxidative fibres. In conclusion, insulin action was not restricted due to insufficient diffusion of the hormone during in vitro incubation in either extensor digitorum longus or soleus muscles from mouse under the specific experimental settings employed in this study. Hence, we suggest that the glycogen depleted core as earlier observed is not due to insufficient insulin action. J. Cell. Biochem. 109: 943,949, 2010. © 2010 Wiley-Liss, Inc. [source] ,-Carotene-Loaded Nanostructured Lipid CarriersJOURNAL OF FOOD SCIENCE, Issue 2 2008A. Hentschel ABSTRACT:, Nanostructured lipid carriers (NLC) technology was used to disperse hydrophobic ,-carotene in an aqueous phase. NLC are lipid nanoparticles with a particle matrix consisting of a blend of a liquid and solid lipid. They were produced by melting the lipid blend at 80 °C and dispersing it into a hot emulsifier solution. The aim of this study was to extend the limited knowledge of melt-emulsified lipidic colloids in food systems and to evaluate the feasibility for further applications as functional ingredient in beverages. Physical stability of the NLC suspension was examined at 2 different storage temperatures by measuring the particle size with photon correlation spectroscopy (PCS) and laser diffractometry (LD). All particles containing sufficient amounts of emulsifier were smaller than 1 ,m (LD diameter 100%) at a mean particle size of around 0.3 ,m (LD) for 9 wk at 20 °C and at least 30 wk at 4 to 8 ° C. Differential scanning calorimetry (DSC) was used to study the solid state of the lipids both in the ,-carotene loaded PGMS and in the NLC particles. Propylene glycol monostearate (PGMS) when dispersed as NLC recrystallized up to 98% during storage time. Within the regarded period of 7 mo no polymorph transitions were observed. Furthermore, stability of the ,-carotene in water dependent on NLC concentration and tocopherol content was measured photospectrometrically to get an estimation of the behavior of NLC in beverages. [source] Evaluation of human fetal neural stem/progenitor cells as a source for cell replacement therapy for neurological disorders: Properties and tumorigenicity after long-term in vitro maintenanceJOURNAL OF NEUROSCIENCE RESEARCH, Issue 2 2009Daisuke Ogawa Abstract It is expected that human neural stem/progenitor cells (hNS/PCs) will some day be used in cell replacement therapies. However, their availability is limited because of ethical issues, so they have to be expanded to obtain sufficient amounts for clinical application. Moreover, in-vitro-maintained hNS/PCs may have a potential for tumorigenicity that could be manifested after transplantation in vivo. In the present study, we demonstrate the in vitro and in vivo properties of long-term-expanded hNS/PCs, including a 6-month bioluminescence imaging (BLI) study of their in vivo tumorigenicity. hNS/PCs cultured for approximately 250 days in vitro (hNS/PCs-250) exhibited a higher growth rate and greater neurogenic potential than those cultured for approximately 500 days in vitro (hNS/PCs-500), which showed greater gliogenic potential. In vivo, both hNS/PCs-250 and -500 differentiated into neurons and astrocytes 4 weeks after being transplanted into the striatum of immunodeficient mice, and hNS/PCs-250 exhibited better survival than hNS/PCs-500 at this time point. We also found that the grafted hNS/PCs-250 survived stably and differentiated properly into neurons and astrocytes even 6 months after the surgery. Moreover, during the 6-month observation period by BLI, we did not detect any evidence of rapid tumorigenic growth of the grafted hNS/PCs, and neither PCNA/Ki67-positive proliferating cells nor significant malignant invasive features were detected histologically. These findings support the idea that hNS/PCs may represent a nontumorigenic, safe, and appropriate cell source for regenerative therapies for neurological disorders. © 2008 Wiley-Liss, Inc. [source] Drought and salinity: A comparison of their effects on mineral nutrition of plantsJOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 4 2005Yuncai Hu Abstract The increasing frequency of dry periods in many regions of the world and the problems associated with salinity in irrigated areas frequently result in the consecutive occurrence of drought and salinity on cultivated land. Currently, 50% of all irrigation schemes are affected by salinity. Nutrient disturbances under both drought and salinity reduce plant growth by affecting the availability, transport, and partitioning of nutrients. However, drought and salinity can differentially affect the mineral nutrition of plants. Salinity may cause nutrient deficiencies or imbalances, due to the competition of Na+ and Cl, with nutrients such as K+, Ca2+, and NO. Drought, on the other hand, can affect nutrient uptake and impair acropetal translocation of some nutrients. Despite contradictory reports on the effects of nutrient supply on plant growth under saline or drought conditions, it is generally accepted that an increased nutrient supply will not improve plant growth when the nutrient is already present in sufficient amounts in the soil and when the drought or salt stress is severe. A better understanding of the role of mineral nutrients in plant resistance to drought and salinity will contribute to an improved fertilizer management in arid and semi-arid areas and in regions suffering from temporary drought. This paper reviews the current state of knowledge on plant nutrition under drought and salinity conditions. Specific topics include: (1) the effects of drought and salt stress on nutrient availability, uptake, transport, and accumulation in plants, (2) the interactions between nutrient supply and drought- or salt-stress response, and (3) means to increase nutrient availability under drought and salinity by breeding and molecular approaches. Trockenstress und Salzstress , Vergleich der Auswirkungen auf die mineralische Ernährung von Pflanzen Eine Zunahme von Trockenperioden in vielen Ländern der Welt und assoziierte Probleme der Versalzung in bewässerten Gebieten führen häufig zu gleichzeitigem Auftreten von Trockenheit und Salinität. Gegenwärtig sind weltweit ungefähr 50 % aller Bewässerungsflächen durch Salinität beeinträchtigt. Nährstoffstörungen bei Trocken- und Salzstress beeinträchtigen die Verfügbarkeit, den Transport und die Verteilung von Nährelementen in der Pflanze und reduzieren somit das Pflanzenwachstum. Trocken- und Salzstress können sich jedoch unterschiedlich auf die Nährstoffversorgung der Pflanzen auswirken. Salinität kann aufgrund der Konkurrenz zwischen Na+ bzw. Cl, und Nährelementen wie K+, Ca2+ und NO Nährstoffmängel oder -ungleichgewichte in den Pflanzen verursachen. Trockenstress kann sowohl die Nährstoffaufnahme als auch den akropetalen Transport einiger Elemente beeinträchtigen. Trotz kontroverser Schlussfolgerungen in der Literatur hinsichtlich der Wechselbeziehungen von Nährstoffangebot und Trocken- bzw. Salzstress auf das Pflanzenwachstum ist allgemein akzeptiert, dass Nährstoffzufuhr das Pflanzenwachstum nicht verbessert, wenn ausreichend Nährstoffe im Boden verfügbar sind oder bei stark ausgeprägter Trockenheit oder Salinität. Ein besseres Verständnis der Rolle von Mineralstoffen in der Toleranz von Pflanzen gegenüber Trocken- oder Salzstress dürfte gerade in ariden und semi-ariden Gebieten sowie in Regionen, die unter periodischer Trockenheit leiden, zu verbesserten Düngestrategien beitragen. In der vorliegenden Arbeit wird der gegenwärtige Kenntnisstand der mineralischen Ernährung bei Trockenheit und Salinität diskutiert. Schwerpunkte der Betrachtungen sind (1) die Auswirkungen von Trockenheit und Salzstress auf die Verfügbarkeit, die Aufnahme, den Transport und die Anreicherung von Nährelementen in der Pflanze, (2) Wechselbeziehungen zwischen dem Nährstoffangebot und Trockenheit oder Salinität sowie (3) Maßnahmen zur Verbesserung der Nährstoffverfügbarkeit bei Trockenheit und Salzstress mittels züchterischer und molekularbiologischer Ansätze. [source] Skin and oral mucosa equivalents: construction and performanceORTHODONTICS & CRANIOFACIAL RESEARCH, Issue 1 2010J Liu To cite this article: Liu J, Bian Z, Kuijpers-Jagtman AM, Von den Hoff JW: Skin and oral mucosa equivalents: construction and performance Orthod Craniofac Res 2010;13:11,20 Abstract Authors,,, Liu J, Bian Z, Kuijpers-Jagtman AM, Von den Hoff JW The skin and the oral mucosa act as a barrier against the external environment. Loss of this barrier function causes dehydration and a high risk of infection. For the treatment of extensive skin wounds such as in severe burns, autologous skin for transplantation is often not available in sufficient amounts. Reconstructions in the oral cavity, as required after tumor resections or cleft palate repair, are often complicated by similar problems. In the last two decades, the field of tissue engineering has provided new solutions to these problems. Techniques have been developed for the culture of epithelial grafts, dermal substitutes, and the combination of these two to a ,functional' skin or mucosa equivalent. The present review focuses on developments in the field of tissue engineering of skin and oral mucosa. The performance of different types of engineered grafts in animal models and clinical studies is discussed. Recent developments such as the use of epithelial stem cells, and gene therapy with transduced skin grafts are also discussed. [source] Phenotypic and functional characterization of mature dendritic cells from pediatric cancer patientsPEDIATRIC BLOOD & CANCER, Issue 7 2007Joannes F.M. Jacobs MD Abstract Background Dendritic cells (DCs) are the most potent antigen-presenting cells of the immune system. Clinical trials have demonstrated that mature DCs loaded with tumor-associated antigens can induce tumor-specific immune responses. Theoretically, pediatric patients are excellent candidates for immunotherapy since their immune system is more potent compared to adults. We studied whether sufficient amounts of mature monocyte-derived DCs can be cultured from peripheral blood of pediatric cancer patients. Procedure DCs from 15 pediatric patients with an untreated primary tumor were cultured from monocytes and matured with clinical grade cytokines. Phenotype and function were tested with flow cytometry, mixed lymphocyte reaction (MLR), and an in vitro migration assay. DCs of children with a solid tumor were compared with monocyte-derived DCs from age-related non-malignant controls. Results Ex vivo-generated monocyte-derived DCs from pediatric patients can be generated in numbers sufficient for DC vaccination trials. Upon cytokine stimulation the DCs highly upregulate the expression of the maturation markers CD80, CD83, and CD86. The mature DCs are six times more potent in inducing T cell proliferation compared to immature DCs. Furthermore, mature DCs, but not immature DCs, express the chemokine receptor CCR7 and have the capacity to migrate in vitro. Conclusions These data indicate that mature DCs can be generated ex vivo to further optimize DC-vaccination trials in pediatric cancer patients. Pediatr Blood Cancer 2007;49:924,927. © 2007 Wiley-Liss, Inc. [source] Vibrio vulnificus infection and metalloproteaseTHE JOURNAL OF DERMATOLOGY, Issue 9 2006Shin-ichi MIYOSHI ABSTRACT Vibrio vulnificus,is ubiquitous in aquatic environments; however, it occasionally causes serious and often fatal infections in humans. These include invasive septicemia contracted through consumption of raw seafood, as well as wound infections acquired through contact with brackish or marine waters. In most cases of septicemia, the patients have underlying disease(s), such as liver dysfunction or alcoholic cirrhosis, and the secondary skin lesions including cellulitis, edema and hemorrhagic bulla appear on the limbs. Although V. Vul,produces various virulent factors including polysaccharide capsule, type IV pili, hemolysin and proteolytic enzymes, the 45-kDa metalloprotease may be a causative factor of the skin lesions, because the purified protease enhances vascular permeability through generation of chemical mediators and also induces serious hemorrhagic damage through digestion of the vascular basement membrane. As well as other bacteria, V. Vul,can regulate the protease production through the quorum-sensing system depending on bacterial cell density. However, this system operates efficiently at 25°C, but not at 37°C. Therefore, V. vulnificus may produce sufficient amounts of the protease only in the interstitial tissue of the limbs, in which temperature is lower than the internal temperature of the human body. [source] Nutritional significance of the selective ingestion of Albizia zygia gum exudate by wild chimpanzees in Bossou, GuineaAMERICAN JOURNAL OF PRIMATOLOGY, Issue 2 2006Kazunari Ushida Abstract The selective ingestion of plant gum exudates by chimpanzees has been frequently observed at various study sites. At Bossou, Guinea, chimpanzees also frequently ingest Albizia zygia gum exudate. A functional explanation for this behavior is lacking, so we evaluated its possible contribution of energy in the form of short-chain fatty acids (SCFA) as well as minerals. An in vitro fermentation study of A. zygia gum using the fecal bacteria of a Bossou chimpanzee showed that carboxylic acids were produced with a 6-hr lag phase up to 44 mmol/l by 18 hr of incubation. Acetate was the most abundant acid produced, followed by lactate and propionate. The energy supplied from the fermentation of a piece of gum exudate (20,30 g) was negligible in comparison with the estimated daily energy requirements of chimpanzees in the wild. However, A. zygia gum exudate (20,30 g) can supply sufficient amounts of calcium, manganese, magnesium, and potassium to fulfill the daily requirements for these minerals in chimpanzees. Am. J. Primatol. 68:143,151, 2006. © 2006 Wiley-Liss, Inc. [source] Signaling requirements and role of salicylic acid in HRT - and rrt -mediated resistance to turnip crinkle virus in ArabidopsisTHE PLANT JOURNAL, Issue 5 2004A.C. Chandra-Shekara Summary Inoculation of turnip crinkle virus (TCV) on the resistant Arabidopsis ecotype Di-17 elicits a hypersensitive response (HR), which is accompanied by increased expression of pathogenesis-related (PR) genes. Previous genetic analyses revealed that the HR to TCV is conferred by HRT, which encodes a coiled-coil (CC), nucleotide-binding site (NBS) and leucine-rich repeat (LRR) class resistance (R) protein. In contrast to the HR, resistance to TCV requires both HRT and a recessive allele at a second locus designated rrt. Here, we demonstrate that unlike most CC-NBS-LRR R genes, HRT/rrt -mediated resistance is dependent on EDS1 and independent of NDR1. Resistance is also independent of RAR1 and SGT1. HRT/rrt -mediated resistance is compromised in plants with reduced salicylic acid (SA) content as a consequence of mutations eds5, pad4, or sid2. By contrast, HR is not affected by mutations in eds1, eds5, pad4, sid2, ndr1, rar1, or sgt1b. Resistance to TCV is restored in both SA-deficient Di-17 plants expressing the nahG transgene and mutants containing the eds1, eds5, or sid2 mutations by exogenous application of SA or the SA analog benzo(1,2,3)thiadiazole-7-carbothioic acid (BTH). In contrast, SA/BTH treatment failed to enhance resistance in HRT pad4, Col-0, or hrt homozygous progeny of a cross between Di-17 and Col-0. Thus, HRT and PAD4 are required for SA-induced resistance. Exogenously supplied SA or high endogenous levels of SA, due to the ssi2 mutation, overcame the suppressive effects of RRT and enhanced resistance to TCV, provided the HRT allele was present. High levels of SA upregulate HRT expression via a PAD4 -dependent pathway. As Col-0 transgenic lines expressing high levels of HRT were resistant to TCV, but lines expressing moderate to low levels of HRT were not, we conclude that SA enhances resistance in the RRT background by upregulating HRT expression. These data suggest that the HRT-TCV interaction is unable to generate sufficient amounts of SA required for a stable resistance phenotype, and the presence of rrt possibly corrects this deficiency. [source] A comparison of cloud-resolving model simulations of trade wind cumulus with aircraft observations taken during RICOTHE QUARTERLY JOURNAL OF THE ROYAL METEOROLOGICAL SOCIETY, Issue 624 2007S. J. Abel Abstract This paper presents results from simulations of trade wind cumulus with the Met Office Large Eddy Model (LEM) based on observed environmental profiles from the Rain In Cumulus over the Ocean (RICO) field experiment. Comparisons of updraught core parameters are made with the in situ data collected onboard the three research aircraft that participated in RICO. The default set-up of the LEM was unable to produce sufficient amounts of rainwater content when compared to measurements by the aircraft. As a main aim of RICO was to quantify the importance of precipitation in the trade cumulus regime, we test the sensitivity of the model to changes in the rain microphysics, the large-scale forcing, and horizontal resolution. By changing these model variables we are able to obtain reasonably good agreement with the observations of updraught core vertical velocity, cloud and rainwater contents. Furthermore, the LEM produces comparable surface precipitation rates to those derived from radar measurements during RICO in a previous study. This gives us some confidence in the ability of the LEM to simulate realistic precipitating trade cumulus. Copyright © 2007 Royal Meteorological Society [source] In vitro Metabolism of Genistein and Tangeretin by Human and Murine Cytochrome P450sBASIC AND CLINICAL PHARMACOLOGY & TOXICOLOGY, Issue 1 2003Vibeke M. Breinholt Analysis of the metabolic profile from incubations with genistein and human liver microsomes revealed the production of five different metabolites, of which three were obtained in sufficient amounts to allow a more detailed elucidation of the structure. One of these metabolites was identified as orobol, the 3,-hydroxylated metabolite of genistein. The remaining two metabolites were also hydroxylated metabolites as evidenced by LC/MS. Orobol was the only metabolite formed after incubation with CYP1A2. The two major product peaks after incubation of tangeretin with human microsomes were identical with 4,-hydroxy-5,6,7,8-tetramethoxyflavone and 5,6-dihydroxy-4,,7,8-trimethoxyflavone, previously identified in rat urine in our laboratory. By comparison with UV spectra and LC/MS fragmentation patterns of previously obtained standards, the remaining metabolites eluting after 14, 17 and 20 min. were found to be demethylated at the 4,,7-, 4,,6-positions or hydroxylated at the 3,- and demethylated at the 4,-positions, respectively. Metabolism of tangeretin by recombinant CYP1A2, 3A4, 2D6 and 2C9 resulted in metabolic profiles that qualitatively were identical to those observed in the human microsomes. Inclusion of the CYP1A2 inhibitor fluvoxamine in the incubation mixture with human liver microsomes resulted in potent inhibition of tangeretin and genistein metabolism. Other isozymes-selective CYP inhibitors had only minor effects on tangeretin or genistein metabolism. Overall the presented observations suggest major involvement of CYP1A2 in the hepatic metabolism of these two flavonoids. [source]
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