44 research outputs found

    Identification and molecular cloning of a functional GDP-fucose transporter in Drosophila melanogaster.

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    Nucleotide sugar transporters play a central role in the process of glycosylation. They are responsible for the translocation of nucleotide sugars from the cytosol, their site of synthesis, into the Golgi apparatus where the activated sugars serve as substrates for a variety of glycosyltransferases. We and others have recently identified and cloned the first GDP-fucose transporters of H. sapiens and C. elegans. Based on sequence similarity, we could identify a putative homolog in Drosophila melanogaster showing about 45% identity on protein level. The gene (CG9620) encodes a highly hydrophobic, multi-transmembrane spanning protein of 38.1 kDa that is localized in the Golgi apparatus. In order to test whether this protein serves as a GDP-fucose transporter, we performed complementation studies with fibroblasts from a patient with LADII (leukocyte adhesion deficiency II) which exhibit a strong reduction of fucosylation due to a point mutation in the human GDP-fucose transporter gene. We show that transient transfection of these cells with the Drosophila CG9620 cDNA corrects the GDP-fucose transport defect and reestablishes fucosylation. This study gives experimental proof that the product of the in silico identified Drosophila gene CG9620 serves as a functional GDP-fucose transporter

    Thigh-length compression stockings and DVT after stroke

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    Controversy exists as to whether neoadjuvant chemotherapy improves survival in patients with invasive bladder cancer, despite randomised controlled trials of more than 3000 patients. We undertook a systematic review and meta-analysis to assess the effect of such treatment on survival in patients with this disease

    Erfassung von Schwermetallstroemen in landwirtschaftlichen Tierproduktionsbetrieben und Erarbeitung einer Konzeption zur Verringerung der Schwermetalleintraege durch Wirtschaftsduenger tierischer Herkunft in Agraroekosysteme

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    The overall objectives of the project were to assess heavy metal flows on livestock farms and to develop a strategy to reduce heavy metal inputs into animal manures. For the experiments 20 farms with animal husbandry in various regions of Germany were selected. On the farms the inputs and outputs of the elements copper and zinc, as well as lead, cadmium, chromium and nickel were balanced at the stable level. The effect of abatement measures was evaluated using a calculation tool for stable balances. It is shown, the main input pathways for heavy metals into animal manures are, apart from copper disinfectants, feeding stuffs and feed supplements. Home grown feeds are the major source of heavy metal input into the stable because they are fed in large quantities. However, the heavy metal content of the home grown feeds in particular of roughages for ruminants is low. Purchased feed stuffs (supplementary feeding stuffs and complete feeding stuffs) were found to have a higher content of heavy metals (due to supplementation with trace elements) compared to home grown feeds. Thus, pig and poultry husbandry rather than ruminant husbandry is susceptible to heavy metal accumulation of manures. Heavy metals are cycling within the farm which is of importance when discussing the environmental impact. The turnover within the farm can hardly be controlled by the farmer. Thus, effective strategies have to be targeted at the inputs, e. g. the purchased feed stuffs. A main option to reduce the heavy metal input is to lower the trace element concentrations in supplementary feed stuffs either by legislation of maximum threshold values (e. g. EG 1334/2003) or by volunteer agreements of the feed industry and agriculture. In addition, the absorption of copper and zinc by the animals should be improved using better absorbable trace element compounds and phytase. (orig.)SIGLEAvailable from TIB Hannover: RN 8422(2004,6) / FIZ - Fachinformationszzentrum Karlsruhe / TIB - Technische InformationsbibliothekBundesministerium fuer Umwelt, Naturschutz und Reaktorsicherheit, Berlin (Germany)DEGerman

    Increased Age, but Not Parity Predisposes to Higher Bacteriuria Burdens Due to Streptococcus Urinary Tract Infection and Influences Bladder Cytokine Responses, Which Develop Independent of Tissue Bacterial Loads

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    Streptococcus agalactiae causes urinary tract infection (UTI) in pregnant adults, non-pregnant adults, immune-compromised individuals and the elderly. The pathogenesis of S. agalactiae UTI in distinct patient populations is poorly understood. In this study, we used murine models of UTI incorporating young mice, aged and dam mice to show that uropathogenic S. agalactiae causes bacteriuria at significantly higher levels in aged mice compared to young mice and this occurs coincident with equivalent levels of bladder tissue colonisation at 24 h post-infection (p.i.). In addition, aged mice exhibited significantly higher bacteriuria burdens at 48 h compared to young mice, confirming a divergent pattern of bacterial colonization in the urinary tract of aged and young mice. Multiparous mice, in contrast, exhibited significantly lower urinary titres of S. agalactiae compared to age-matched nulliparous mice suggesting that parity enhances the ability of the host to control S. agalactiae bacteriuria. Additionally, we show that both age and parity alter the expression levels of several key regulatory and pro-inflammatory cytokines, which are known to be important the immune response to UTI, including Interleukin (IL)-1β, IL-12(p40), and Monocyte Chemoattractant Protein-1 (MCP-1). Finally, we demonstrate that other cytokines, including IL-17 are induced significantly in the S. agalactiae-infected bladder regardless of age and parity status. Collectively, these findings show that the host environment plays an important role in influencing the severity of S. agalactiae UTI; infection dynamics, particularly in the context of bacteriuria, depend on age and parity, which also affect the nature of innate immune responses to infection
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