4,184 research outputs found

    A theoretical model of a new electrostatic transducer incorporating fluidic amplification

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    This article concerns the design of a new electrostatic transducer whose backplate consists of a series of drilled pipes. A new one-dimensional model is derived which considers the interaction of the membrane with the air load, the air cavities, and the drilled pipes in the backplate. Dynamic equations for the impedance in each component of the device are calculated analytically and connected using interface conditions of continuity of pressure and radiation conditions into the air load. The model is able to produce solutions to the mechanical impedance of the device and the displacement of the membrane as a function of the device's design parameters. Model results for the output pressure compare well with previous experimental data. The inverse problem of retrieving the design parameters for a desired output is discussed

    Reference gene selection and RNA preservation protocol in the cat flea, Ctenocephalides felis, for gene expression studies

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    This work was supported by a Knowledge Transfer Network BBSRC Industrial Case (#414 BB/L502467/1) studentship in association Zoetis Inc.Peer reviewedPostprin

    Intergovernmental and Functional Aspects of Public Employment Trends in the United States

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    There is a great deal of policy concern over the issue of employment and compensation levels in the public sector. This concern covers topics ranging from rising direct labor costs and pension benefits, to the unbalanced growth of central city government and other service sector employment, to power inequality in collective bargaining, to the lack of incentive for productivity improvement. While there have been substantive case studies which have made effective use of local data to deal with certain of these issues, aggregate work on the trends in state-local government public employment has been less satisfactory. Any analysis of state and local government employment problems on an aggregate basis depends on the extent and quality of data available. In this context, this article will undertake two tasks: a description of the trends in public employment, and an assessment of the value and comparability of those data which are presently available

    Changes to DPPC domain structure in the presence of carbon nanoparticles

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    DPPC (dipalmitoylphosphatidylcholine) is a disaturated lipid capable of forming closely packed monolayers at the air–liquid interface of the lung and allows the surface tension within the alveoli to reduce to almost zero and thus prevent alveolar collapse. Carbon nanoparticles are formed in natural and man-made combustion events, including diesel engines, and are capable of reaching the alveolar epithelium during breathing. In this work, we have used Brewster angle microscopy and neutron reflectivity to study the effect of differing concentrations of carbon nanoparticles on the structure of DPPC monolayer as the monolayer is subject to compression and expansion. The results show that the inclusion of carbon nanoparticles within a DPPC monolayer affects the formation and structure of the lipid domains. The domains lose their circular structure and show a crenated structure as well as a reduction in overall size of the domains. This change in structure is also evident following expansion of the lipid monolayer, suggesting that some carbon nanoparticles may remain associated with the monolayer. This observation could have an important implication regarding the removal of nanosized airborne pollutants from the human lung

    Protein Kinase A Activity and Anchoring Are Required for Ovarian Cancer Cell Migration and Invasion

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    Epithelial ovarian cancer (EOC) is the deadliest of the gynecological malignancies, due in part to its clinically occult metastasis. Therefore, understanding the mechanisms governing EOC dissemination and invasion may provide new targets for antimetastatic therapies or new methods for detection of metastatic disease. The cAMP-dependent protein kinase (PKA) is often dysregulated in EOC. Furthermore, PKA activity and subcellular localization by A-kinase anchoring proteins (AKAPs) are important regulators of cytoskeletal dynamics and cell migration. Thus, we sought to study the role of PKA and AKAP function in both EOC cell migration and invasion. Using the plasma membrane-directed PKA biosensor, pmAKAR3, and an improved migration/invasion assay, we show that PKA is activated at the leading edge of migrating SKOV-3 EOC cells, and that inhibition of PKA activity blocks SKOV-3 cell migration. Furthermore, we show that while the PKA activity within the leading edge of these cells is mediated by anchoring of type-II regulatory PKA subunits (RII), inhibition of anchoring of either RI or RII PKA subunits blocks cell migration. Importantly, we also show – for the first time – that PKA activity is up-regulated at the leading edge of SKOV-3 cells during invasion of a three-dimensional extracellular matrix and, as seen for migration, inhibition of either PKA activity or AKAP-mediated PKA anchoring blocks matrix invasion. These data are the first to demonstrate that the invasion of extracellular matrix by cancer cells elicits activation of PKA within the invasive leading edge and that both PKA activity and anchoring are required for matrix invasion. These observations suggest a role for PKA and AKAP activity in EOC metastasis

    Characterization of acyl chain position in unsaturated phosphatidylcholines using differential mobility-mass spectrometry

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    Glycerophospholipids (GPs) that differ in the relative position of the two fatty acyl chains on the glycerol backbone (i.e., sn-positional isomers) can have distinct physicochemical properties. The unambiguous assignment of acyl chain position to an individual GP represents a significant analytical challenge. Here we describe a workflow where phosphatidylcholines (PCs) are subjected to ESI for characterization by a combination of differential mobility spectrometry and MS (DMS-MS). When infused as a mixture, ions formed from silver adduction of each phospholipid isomer {e.g., [PC (16:0/18:1) + Ag]+ and [PC (18:1/16:0) + Ag]+} are transmitted through the DMS device at discrete compensation voltages. Varying their relative amounts allows facile and unambiguous assignment of the sn-positions of the fatty acyl chains for each isomer. Integration of the well-resolved ion populations provides a rapid method (\u3c 3 min) for relative quantification of these lipid isomers. The DMS-MS results show excellent agreement with established, but time-consuming, enzymatic approaches and also provide superior accuracy to methods that rely on MS alone. The advantages of this DMS-MS method in identification and quantification of GP isomer populations is demonstrated by direct analysis of complex biological extracts without any prior fractionation

    Structure of the regulatory hyaluronan binding domain in the inflammatory leukocyte homing receptor CD44

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    Adhesive interactions involving CD44, the cell surface receptor for hyaluronan, underlie fundamental processes such as inflammatory leukocyte homing and tumor metastasis. Regulation of such events is critical and appears to be effected by changes in CD44 N-glycosylation that switch the receptor "on" or "off" under appropriate circumstances. How altered glycosylation influences binding of hyaluronan to the lectin-like Link module in CD44 is unclear, although evidence suggests additional flanking sequences peculiar to CD44 may be involved. Here we show using X-ray crystallography and NMR spectroscopy that these sequences form a lobular extension to the Link module, creating an enlarged HA binding domain and a formerly unidentified protein fold. Moreover, the disposition of key N-glycosylation sites reveals how specific sugar chains could alter both the affinity and avidity of CD44 HA binding. Our results provide the necessary structural framework for understanding the diverse functions of CD44 and developing novel therapeutic strategies

    Sample size calculations for cluster randomised controlled trials with a fixed number of clusters

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    Background\ud Cluster randomised controlled trials (CRCTs) are frequently used in health service evaluation. Assuming an average cluster size, required sample sizes are readily computed for both binary and continuous outcomes, by estimating a design effect or inflation factor. However, where the number of clusters are fixed in advance, but where it is possible to increase the number of individuals within each cluster, as is frequently the case in health service evaluation, sample size formulae have been less well studied. \ud \ud Methods\ud We systematically outline sample size formulae (including required number of randomisation units, detectable difference and power) for CRCTs with a fixed number of clusters, to provide a concise summary for both binary and continuous outcomes. Extensions to the case of unequal cluster sizes are provided. \ud \ud Results\ud For trials with a fixed number of equal sized clusters (k), the trial will be feasible provided the number of clusters is greater than the product of the number of individuals required under individual randomisation (nin_i) and the estimated intra-cluster correlation (ρ\rho). So, a simple rule is that the number of clusters (κ\kappa) will be sufficient provided: \ud \ud κ\kappa > nin_i x ρ\rho\ud \ud Where this is not the case, investigators can determine the maximum available power to detect the pre-specified difference, or the minimum detectable difference under the pre-specified value for power. \ud \ud Conclusions\ud Designing a CRCT with a fixed number of clusters might mean that the study will not be feasible, leading to the notion of a minimum detectable difference (or a maximum achievable power), irrespective of how many individuals are included within each cluster. \ud \u

    Cerebral Abscess and \u3ci\u3eCephenemyia phobifer\u3c/i\u3e in a Mule Deer in Central Nebraska

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    A wild yearling male mule deer (Odocoileus hemionus) from south central Nebraska was submitted to the University of Nebraska North Platte Station Diagnostic Laboratory with the history of severe depression, slight incoordination, and visual impairment. Gross examination revealed a large abcess involving approximately 65-75% of the cebral hemispheres of the brain and approximately bots in the retropharyngeal pouches

    Cerebral Abscess and \u3ci\u3eCephenemyia phobifer\u3c/i\u3e in a Mule Deer in Central Nebraska

    Get PDF
    A wild yearling male mule deer (Odocoileus hemionus) from south central Nebraska was submitted to the University of Nebraska North Platte Station Diagnostic Laboratory with the history of severe depression, slight incoordination, and visual impairment. Gross examination revealed a large abcess involving approximately 65-75% of the cebral hemispheres of the brain and approximately bots in the retropharyngeal pouches
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