86 research outputs found

    Mechanisms of leukocyte lipid body formation and function in inflammation

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    An area of increasingly interest for the understanding of cell signaling are the spatio-temporal aspects of the different enzymes involved in lipid mediator generation (eicosanoid-forming enzymes, phospholipases and their regulatory kinases and phosphatases) and pools of lipid precursors. The compartmentalization of signaling components within discrete and dynamic sites in the cell is critical for specificity and efficiency of enzymatic reactions of phosphorilation, enzyme activation and function. We hypothesized that lipid bodies - inducible non-membrane bound cytoplasmic lipid domains - function as specialized intracellular sites of compartmentalization of signaling with major roles in lipid mediator formation within leukocytes engaged in inflammatory process. Over the past years substantial progresses have been made demonstrating that all enzymes involved in eicosanoid synthesis localize at lipid bodies and lipid bodies are distinct sites for eicosanoid generation. Here we will review our current knowledge on the mechanisms of formation and functions of lipid bodies pertinent to inflammation

    Characterization of the effects of cross-linking of macrophage CD44 associated with increased phagocytosis of apoptotic PMN

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    Control of macrophage capacity for apoptotic cell clearance by soluble mediators such as cytokines, prostaglandins and lipoxins, serum proteins, and glucocorticoids may critically determine the rate at which inflammation resolves. Previous studies suggested that macrophage capacity for clearance of apoptotic neutrophils was profoundly altered following binding of CD44 antibodies. We have used a number of different approaches to further define the mechanism by which CD44 rapidly and specifically augment phagocytosis of apoptotic neutrophils. Use of Fab ’ fragments unequivocally demonstrated a requirement for cross-linking of macrophage surface CD44. The molecular mechanism of CD44-augmented phagocytosis was shown to be opsonin-independent and to be distinct from the Mer/protein S pathway induced by glucocorticoids and was not functional for clearance of apoptotic eosinophils. CD44-cross-linking also altered macrophage migration and induced cytoskeletal re-organisation together with phosphorylation of paxillin and activation of Rac2. Investigation of signal transduction pathways that might be critical for CD44 augmentation of phagocytosis revealed that Ca 2+ signalling, PI-3 kinase pathways and altered cAMP signalling were not involved, but did implicate a key role for tyrosine phosphorylation events. Finally, although CD44 antibodies were able to augment phagocytosis of apoptotic neutrophils by murine peritoneal and bone marrow-derived macrophages, we did not observe a difference in the clearance of neutrophils following induction of peritonitis with thioglycollate in CD44-deficient animals. Together, these data demonstrate that CD4

    Cysteinyl leukotrienes: multi-functional mediators in allergic rhinitis

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    Cysteinyl leukotrienes (CysLTs) are a family of inflammatory lipid mediators synthesized from arachidonic acid by a variety of cells, including mast cells, eosinophils, basophils, and macrophages. This article reviews the data for the role of CysLTs as multi-functional mediators in allergic rhinitis (AR). We review the evidence that: (1) CysLTs are released from inflammatory cells that participate in AR, (2) receptors for CysLTs are located in nasal tissue, (3) CysLTs are increased in patients with AR and are released following allergen exposure, (4) administration of CysLTs reproduces the symptoms of AR, (5) CysLTs play roles in the maturation, as well as tissue recruitment, of inflammatory cells, and (6) a complex inter-regulation between CysLTs and a variety of other inflammatory mediators exists.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75432/1/j.1365-2222.2006.02498.x.pd

    The potential of metering roundabouts: influence in transportation externalities

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    Roundabouts are increasingly being used on busy arterial streets for traffic calming purposes. However, if one roundabout leg is near a distribution hub, e.g. parking areas of shopping centers, the entry traffic volumes will be particularly high in peak hours. This paper investigated a partial-metering based strategy to reduce traffic-related costs in a corridor. Specifically, the resulting traffic performance, energy, environmental and exposure impacts associated with access roundabouts were studied in an urban commercial area, namely: a) to characterize corridor operations in terms of link-specific travel time, fuel consumption, carbon dioxide and nitrogen oxides emissions, and noise costs; b) to propose an optimization model to minimize above outputs; and c) to demonstrate the model applicability under different traffic demand and directional splits combinations. Traffic, noise and vehicle dynamics data were collected from a corridor with roundabouts and signalized intersections near a commercial area of Guimarães, Portugal. Microscopic traffic and emission modeling platforms were used to model traffic operations and estimate pollutant emissions, respectively. Traffic noise was estimated with a semi-dynamical model. Link-based cost functions were developed based on the integrated modeling structure. Lastly, a Sequential quadratic programming type approach was applied to find optimal timing settings. The benefit of the partial-metering system, in terms of costs, could be up to 13% with observed traffic volumes. The efficiency of the proposed system increased as entering traffic at the metered approaches increased (~7% less costs). The findings let one to quantify metering benefits near shopping areas
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