12 research outputs found

    RAGE and ICAM-1 differentially control leukocyte recruitment during acute inflammation in a stimulus-dependent manner

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    <p>Abstract</p> <p>Background</p> <p>The receptor for advanced glycation endproducts, RAGE, is involved in the pathogenesis of many inflammatory conditions, which is mostly related to its strong activation of NF-κB but also due to its function as ligand for the β<sub>2</sub>-integrin Mac-1. To further dissect the stimulus-dependent role of RAGE on leukocyte recruitment during inflammation, we investigated β<sub>2</sub>-integrin-dependent leukocyte adhesion in <it>RAGE<sup>-/- </sup></it>and <it>Icam1<sup>-/- </sup></it>mice in different cremaster muscle models of inflammation using intravital microscopy.</p> <p>Results</p> <p>We demonstrate that RAGE, but not ICAM-1 substantially contributes to N-formyl-methionyl-leucyl-phenylalanine (fMLP)-induced leukocyte adhesion in TNF-α-pretreated cremaster muscle venules in a Mac-1-dependent manner. In contrast, fMLP-stimulated leukocyte adhesion in unstimulated cremaster muscle venules is independent of RAGE, but dependent on ICAM-1 and its interaction with LFA-1. Furthermore, chemokine CXCL1-stimulated leukocyte adhesion in surgically prepared cremaster muscle venules was independent of RAGE but strongly dependent on ICAM-1 and LFA-1 suggesting a differential and stimulus-dependent regulation of leukocyte adhesion during inflammation in vivo.</p> <p>Conclusion</p> <p>Our results demonstrate that RAGE and ICAM-1 differentially regulate leukocyte adhesion in vivo in a stimulus-dependent manner.</p

    [3H]idazoxan and some other alpha 2-adrenergic drugs also bind with high affinity to a nonadrenergic site

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    We compared the pharmacological properties of the alpha 2-adrenergic radioligand [3H]idazoxan with those of [3H]rauwolscine in rat and [3H]yohimbine in human renal cortical membranes. The density of "specific" [3H]idazoxan binding sites (defined by 100 microM tolazoline) was twice as high as that of [3H]rauwolscine in rat kidney and four times as high as that of [3H]yohimbine in human kidney. A variety of structurally different drugs fully competed for specific [3H]rauwolscine and [3H]yohimbine binding, with affinities appropriate for the interaction with alpha 2-adrenergic receptors. Specific [3H]idazoxan binding, however, was only partially competed for by the catecholamines epinephrine and norepinephrine in both tissues. Thus, [3H]idazoxan labels both alpha 2-adrenergic receptors and a nonadrenergic site. Clonidine, B-HT 920, moxonidine, phentolamine, prazosin, yohimbine, dopamine, and serotonin also could not compete for this site. However, UK 14,304, guanabenz, indanidine, tolazoline, oxymetazoline, and SK&F 104,078 competed for the additional [3H]idazoxan sites with affinities similar to those at alpha 2-adrenergic receptors. [3H]idazoxan binding substantially in excess of [3H]rauwolscine or [3H]yohimbine binding was also found in human platelets, myometrium, and erythroleukemia (HEL) cells but not in three cell lines lacking alpha 2-receptors (MDCK, BC3H1, and Jurkat cells). Although we have been unsuccessful thus far in defining the precise nature of the additional [3H]idazoxan binding sites, we hypothesize that these sites may be closely affiliated with alpha 2-adrenergic receptors but clearly distinct from the catecholamine binding site of the receptor. The results indicate that care must be taken in the use of [3H]idazoxan or drugs that are recognized at its nonadrenergic site when studying alpha 2-adrenergic effects and receptor subtype

    A Sediment Budget of the Upper Kaunertal

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    This chapter presents the sediment budget of the Upper Kaunertal (Ötztal Alps, Austria) for the years 2012–2014 as obtained in the framework of the PROSA (high-resolution measurements of morphodynamics in rapidly changing PROglacial Systems of the Alps) research project. An important methodological basis of this high-mountain sediment budget is the usage of study area-wide LiDAR data (TLS and ALS) of comparatively high temporal and spatial resolution to measure rates of erosion and deposition, and to regionalize/upscale rates at the local scale. After several billion measurement points and data from fieldwork, mapping, and modeling efforts had been processed and evaluated, it was possible to identify and quantify sediment transfer by all relevant processes at the scale of the 62 km2 study area. These processes include rockfall of three different magnitude classes, debris flows, avalanches, creep on talus, fluvial processes (hillslopes and main fluvial system), rock glaciers, and glaciers. After a short presentation of the process-specific methods to obtain catchment-wide rates, we discuss process-specific results and the budget. The sediment budget does not only show the relative importance of the mentioned processes and spatial subunits (proglacial vs. non-proglacial) in the Upper Kaunertal. It also gives insight into the importance of high-magnitude events and the configuration of the sediment transport system
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