130 research outputs found

    Stem cell factor and its soluble receptor (c-kit) in serum of asthmatic patients- correlation with disease severity

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    <p>Abstract</p> <p>Background</p> <p>SCF (stem cell factor) is a pleiotropic cytokine exerting its role at different stages of bone marrow development and affecting eosinophil activation, mast cells and basophil chemotaxis and survival. The aim of the study was to assess concentration of SCF and its soluble receptor c-kit (sc-kit) in peripheral blood of patients with asthma referring it to asthma severity and phenotype.</p> <p>Methods</p> <p>The study involved 107 patients with bronchial asthma, well characterized with respect to severity and 21 healthy controls. Concentration of SCF and sc-kit in the patients serum were measured by ELISA method.</p> <p>Results</p> <p>Mean serum SCF level in the group of asthmatics (n = 88) was significantly higher as compared to healthy controls (1010 pg/ml ± 37 vs 799 ± 33; p < 0,001). The level of SCF was higher in patients with severe asthma as compared to patients with non-severe asthma (1054 +/- 41 pg/ml vs 819 +/- 50; p < 0,01) and correlated with dose of inhaled glucocorticosteroids taken by the patients to achieve asthma control (R = 0,28; p < 0,01). The mean sc-kit serum level did not differ between asthmatic patients and healthy controls, however the level of sc-kit in non-severe asthmatics was significantly higher as compared to patients with severe asthma and healthy controls. In asthmatic patients (n = 63) the level of sc-kit correlated positively with FEV1% predicted value (R = 0,45; p < 0,001) and MEF25% predicted value (R = 0,33; p < 0,01). The level of sc-kit inversely correlated with the dose of inhaled glucocorticosteroids taken by the patients (R = -0,26; p < 0,01).</p> <p>Conclusion</p> <p>Serum levels of SCF and its soluble receptor c-kit seem to be reflect asthma severity suggesting a role for these molecules in asthmatic inflammation.</p

    Screening for foot problems in children: is this practice justifiable?

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    Podiatry screening of children is a common practice, which occurs largely without adequate data to support the need for such activity. Such programs may be either formalised, or more ad hoc in nature, depending upon the use of guidelines or existing models. Although often not used, the well-established criteria for assessing the merits of screening programs can greatly increase the understanding as to whether such practices are actually worthwhile. This review examines the purpose of community health screening in the Australian context, as occurs for tuberculosis, breast, cervical and prostate cancers, and then examines podiatry screening practices for children with reference to the criteria of the World Health Organisation (WHO). Topically, the issue of paediatric foot posture forms the focus of this review, as it presents with great frequency to a range of clinicians. Comparison is made with developmental dysplasia of the hip, in which instance the WHO criteria are well met. Considering that the burden of the condition being screened for must be demonstrable, and that early identification must be found to be beneficial, in order to justify a screening program, there is no sound support for either continuing or establishing podiatry screenings for children

    Selective deployment of transcription factor paralogs with submaximal strength facilitates gene regulation in the immune system

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    In multicellular organisms, duplicated genes can diverge through tissue-specific gene expression patterns, as exemplified by highly regulated expression of Runx transcription factor paralogs with apparent functional redundancy. Here we asked what cell type-specific biologies might be supported by the selective expression of Runx paralogs during Langerhans cell and inducible regulatory T cell differentiation. We uncovered functional non-equivalence between Runx paralogs. Selective expression of native paralogs allowed integration of transcription factor activity with extrinsic signals, while non-native paralogs enforced differentiation even in the absence of exogenous inducers. DNA-binding affinity was controlled by divergent amino acids within the otherwise highly conserved RUNT domain, and evolutionary reconstruction suggested convergence of RUNT domain residues towards sub-maximal strength. Hence, the selective expression of gene duplicates in specialized cell types can synergize with the acquisition of functional differences to enable appropriate gene expression, lineage choice and differentiation in the mammalian immune system

    Platelet activation: ultrastructure and morphometry in platelet-rich plasma of horses

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    This study was conducted to investigate the activation ability of the platelet-rich plasma (PRP) by pharmacological agents, as well as to verify the need or not of this activation for therapeutic use. The PRP was obtained from four healthy crossbred geldings aged 13 to 16 years (15±1years), and was processed for observation and quantification of the platelet morphology by using the transmission electron microscopy. All PRP samples were activated with 10% calcium chloride (CaCl2) solution, pure bovine thrombin or associated with CaCl2. The control (pure PRP) was not pharmacologically activated. In the pure PRP samples, 49% of the platelets were classified as state of activation uncertain, 41% as resting, 9% as fully activated and 1% as irreversibly damaged. Treatment with 10% CaCl2 provided a distribution of 54% platelets in state of activation uncertain, 24% as fully activated, 20% as resting, and 2% as irreversibly damaged. The platelet morphology of the bovine thrombin treated samples did not fit into classification adopted, as showing irregular shape with emission of large filamentous pseudopods, appearance of ruptured and whole granules in the remaining cytoplasm and extracellular environment. There was effect of the treatment on the platelet morphology (P=0.03). The 10% CaCl2 is an adequate platelet-activating agent. However, in cases the use of PRP under its liquid form is necessary, the use of pure PRP is recommended, since besides presenting an adequate percentage of fully activated platelets it also has significant amount of the resting type, which can be activated by substances found in the injured tissue

    Bone substitutes in orthopaedic surgery: from basic science to clinical practice

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    Holocene climate variability as derived from alkenone sea surface temperature reconstructions and coupled ocean-atmosphere model experiments

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    Holocene climate modes are identified by the statistical analysis of reconstructed sea surface temperatures (SSTs) from the tropical and North Atlantic regions. The leading mode of Holocene SST variability in the tropical region indicates a rapid warming from the early to the mid Holocene followed by a relatively weak warming during the late Holocene. The dominant mode of the North Atlantic region SST captures the transition from relatively warm (cold) conditions in the eastern North Atlantic and the western Mediterranean Sea (the northern Red Sea) to relatively cold (warm) conditions in these regions from the early to late Holocene. This pattern of Holocene SST variability resembles the signature of the Arctic Oscillation/North Atlantic Oscillation (AO/NAO). The second mode of both tropical and North Atlantic regions captures the warming towards the mid Holocene and subsequent neoglaciation. The dominant modes of Holocene SST variability emphasize enhanced variability around 2300 and 1000 years. The leading mode of the coupled tropical-North Atlantic Holocene SST variability shows that an increase of tropical SST is accompanied by a decrease of SST in the eastern North Atlantic. An analogy with the instrumental period as well as the analysis of a long-term integration of a coupled ocean-atmosphere general circulation model suggest that the AO/NAO is one dominant mode of climate variability at millennial time scales

    Turbulent diffusion in near-wall turbulence

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    Acceleration technique for Milankovitch type forcing in a coupled atmosphere-ocean circulation model: method and application for the Holocene

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    A method is introduced which allows the calculation of long-term climate trends within the framework of a coupled atmosphere-ocean circulation model. The change in the seasonal cycle of incident solar radiation induced by varying orbital parameters has been accelerated by factors of 10 and 100 in order to allow transient simulations over the period from the mid-Holocene until today, covering the last 7000 years. In contrast to conventional time-slice experiments, this approach is not restricted to equilibrium simulations and is capable to utilise all available data for validation. We find that opposing Holocene climate trends in tropics and extra-tropics are a robust feature in our experiments. Results from the transient simulations of the mid-Holocene climate at 6000 years before present show considerable differences to atmosphere-alone model simulations, in particular at high latitudes, attributed to atmosphere-ocean-sea ice effects. The simulations were extended for the time period 1800 to 2000 AD, where, in contrast to the Holocene climate, increased concentrations of greenhouse gases in the atmosphere provide for the strongest driving mechanism. The experiments reveal that a Northern Hemisphere cooling trend over the Holocene is completely cancelled by the warming trend during the last century, which brings the recent global warming into a long-term context

    Optical FDM/TDM crossconnect employing a delayed self-duplex light source and an optical timeslot interchanger

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