137 research outputs found
Self-stabilised fractality of sea-coasts through damped erosion
Erosion of rocky coasts spontaneously creates irregular seashores. But the
geometrical irregularity, in turn, damps the sea-waves, decreasing the average
wave amplitude. There may then exist a mutual self-stabilisation of the waves
amplitude together with the irregular morphology of the coast. A simple model
of such stabilisation is studied. It leads, through a complex dynamics of the
earth-sea interface, to the appearance of a stationary fractal seacoast with
dimension close to 4/3. Fractal geometry plays here the role of a morphological
attractor directly related to percolation geometry.Comment: 4 pages, 5 figure
The thermodynamics of ammonium scheelites V. Heat capacity of deuterated ammonium metaperiodate ND4IO4 from 8 to 329 K
The heat capacity of the scheelite salt: deuterated ammonium metaperiodate, ND4IO4, was measured from 8 to 329 K using adiabatic calorimetry. The heat capacity against temperature curve shows a broad maximum with a peak around 200 K which is typical of other ammonium scheelites. A small peak in the curve around 275 K resulted from fusion of a saturated D2O salt solution trapped in the lattice. Values of the standard molar thermodynamic quantities for ND4IO4 are presented up to 330 K.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/26999/1/0000566.pd
The thermodynamics of ammonium scheelites IV. Heat capacity of ammonium metaperiodate NH4IO4 from 8 to 324 K
The heat capacity of the scheelite salt ammonium metaperiodate, NH4IO4, was measured from 8 to 324 K using adiabatic calorimetry. The heat capacity against temperature curve shows an excess with a maximum around 200 K as is typical of other ammonium scheelites. A small peak in the curve near 270 K resulted from melting a saturated aqueous solution trapped in the lattice. Values of the standard molar thermodynamic quantities for NH4IO4 are presented up to 320 K. Values for Cp, mo(298.15 K)/R, [Delta]0TSmo(298.15 K)/R, and [Phi]mo(298.15 K, 0)/R are (18.58+/-0.02), (23.03+/-0.04), and (11.20+/-0.02), respectively.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/26984/1/0000551.pd
Regulation of neutrophil senescence by microRNAs
Neutrophils are rapidly recruited to sites of tissue injury or infection, where they protect against invading pathogens. Neutrophil functions are limited by a process of neutrophil senescence, which renders the cells unable to respond to chemoattractants, carry out respiratory burst, or degranulate. In parallel, aged neutrophils also undergo spontaneous apoptosis, which can be delayed by factors such as GMCSF. This is then followed by their subsequent removal by phagocytic cells such as macrophages, thereby preventing unwanted inflammation and tissue damage. Neutrophils translate mRNA to make new proteins that are important in maintaining functional longevity. We therefore hypothesised that neutrophil functions and lifespan might be regulated by microRNAs expressed within human neutrophils. Total RNA from highly purified neutrophils was prepared and subjected to microarray analysis using the Agilent human miRNA microarray V3. We found human neutrophils expressed a selected repertoire of 148 microRNAs and that 6 of these were significantly upregulated after a period of 4 hours in culture, at a time when the contribution of apoptosis is negligible. A list of predicted targets for these 6 microRNAs was generated from http://mirecords.biolead.org and compared to mRNA species downregulated over time, revealing 83 genes targeted by at least 2 out of the 6 regulated microRNAs. Pathway analysis of genes containing binding sites for these microRNAs identified the following pathways: chemokine and cytokine signalling, Ras pathway, and regulation of the actin cytoskeleton. Our data suggest that microRNAs may play a role in the regulation of neutrophil senescence and further suggest that manipulation of microRNAs might represent an area of future therapeutic interest for the treatment of inflammatory disease
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Bioavailability in soils
The consumption of locally-produced vegetables by humans may be an important exposure pathway for soil contaminants in many urban settings and for agricultural land use. Hence, prediction of metal and metalloid uptake by vegetables from contaminated soils is an important part of the Human Health Risk Assessment procedure. The behaviour of metals (cadmium, chromium, cobalt, copper, mercury, molybdenum, nickel, lead and zinc) and metalloids (arsenic, boron and selenium) in contaminated soils depends to a large extent on the intrinsic charge, valence and speciation of the contaminant ion, and soil properties such as pH, redox status and contents of clay and/or organic matter. However, chemistry and behaviour of the contaminant in soil alone cannot predict soil-to-plant transfer. Root uptake, root selectivity, ion interactions, rhizosphere processes, leaf uptake from the atmosphere, and plant partitioning are important processes that ultimately govern the accumulation ofmetals and metalloids in edible vegetable tissues. Mechanistic models to accurately describe all these processes have not yet been developed, let alone validated under field conditions. Hence, to estimate risks by vegetable consumption, empirical models have been used to correlate concentrations of metals and metalloids in contaminated soils, soil physico-chemical characteristics, and concentrations of elements in vegetable tissues. These models should only be used within the bounds of their calibration, and often need to be re-calibrated or validated using local soil and environmental conditions on a regional or site-specific basis.Mike J. McLaughlin, Erik Smolders, Fien Degryse, and Rene Rietr
Activation of adherent vascular neutrophils in the lung during acute endotoxemia
BACKGROUND: Neutrophils constitute the first line of defense against invading microorganisms. Whereas these cells readily undergo apoptosis under homeostatic conditions, their survival is prolonged during inflammatory reactions and they become biochemically and functionally activated. In the present study, we analyzed the effects of acute endotoxemia on the response of a unique subpopulation of neutrophils tightly adhered to the lung vasculature. METHODS: Rats were treated with 5 mg/kg lipopolysaccharide (i.v.) to induce acute endotoxemia. Adherent neutrophils were isolated from the lung vasculature by collagenase digestion and sequential filtering. Agarose gel electrophoresis, RT-PCR, western blotting and electrophoretic mobility shift assays were used to evaluate neutrophil activity. RESULTS: Adherent vascular neutrophils isolated from endotoxemic animals exhibited decreased apoptosis when compared to cells from control animals. This was associated with a marked increase in expression of the anti-apoptotic protein, Mcl-1. Cells isolated 0.5–2 hours after endotoxin administration were more chemotactic than cells from control animals and expressed increased tumor necrosis factor-alpha and cyclooxygenase-2 mRNA and protein, demonstrating that they are functionally activated. Endotoxin treatment of the animals also induced p38 and p44/42 mitogen activated protein kinases in the adherent lung neutrophils, as well as nuclear binding activity of the transcription factors, NF-κB and cAMP response element binding protein. CONCLUSION: These data demonstrate that adherent vascular lung neutrophils are highly responsive to endotoxin and that pathways regulating apoptosis and cellular activation are upregulated in these cells
Different Molecular Signatures in Magnetic Resonance Imaging-Staged Facioscapulohumeral Muscular Dystrophy Muscles
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common muscular dystrophies and is characterized by a non-conventional genetic mechanism activated by pathogenic D4Z4 repeat contractions. By muscle Magnetic Resonance Imaging (MRI) we observed that T2-short tau inversion recovery (T2-STIR) sequences identify two different conditions in which each muscle can be found before the irreversible dystrophic alteration, marked as T1-weighted sequence hyperintensity, takes place. We studied these conditions in order to obtain further information on the molecular mechanisms involved in the selective wasting of single muscles or muscle groups in this disease
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