19 research outputs found

    Air Leakage Calculations for NBS Administration Building U.S.A

    No full text

    Thermal Performance of Fine‐Grained Soils

    No full text

    Simplified analysis of thermal and lighting characteristics of windows : two case studies /

    No full text
    Spine title: Thermal and lighting characteristics of windows.Includes bibliographical references (p. 65-66 (1st group)).Mode of access: Internet

    Kawasaki Disease-Specific Molecules in the Sera Are Linked to Microbe-Associated Molecular Patterns in the Biofilms

    No full text
    <div><p>Background</p><p>Kawasaki disease (KD) is a systemic vasculitis of unknown etiology. The innate immune system is involved in its pathophysiology at the acute phase. We have recently established a novel murine model of KD coronary arteritis by oral administration of a synthetic microbe-associated molecular pattern (MAMP). On the hypothesis that specific MAMPs exist in KD sera, we have searched them to identify KD-specific molecules and to assess the pathogenesis.</p><p>Methods</p><p>We performed liquid chromatography-mass spectrometry (LC-MS) analysis of fractionated serum samples from 117 patients with KD and 106 controls. Microbiological and LC-MS evaluation of biofilm samples were also performed.</p><p>Results</p><p>KD samples elicited proinflammatory cytokine responses from human coronary artery endothelial cells (HCAECs). By LC-MS analysis of KD serum samples collected at 3 different periods, we detected a variety of KD-specific molecules in the lipophilic fractions that showed distinct m/z and MS/MS fragmentation patterns in each cluster. Serum KD-specific molecules showed m/z and MS/MS fragmentation patterns almost identical to those of MAMPs obtained from the biofilms formed <i>in vitro</i> (common MAMPs from <i>Bacillus cereus</i>, <i>Yersinia pseudotuberculosis</i> and <i>Staphylococcus aureus</i>) at the 1<sup>st</sup> study period, and from the biofilms formed <i>in vivo</i> (common MAMPs from <i>Bacillus cereus</i>, <i>Bacillus subtilis/Bacillus cereus/Yersinia pseudotuberculosis</i> and <i>Staphylococcus aureus</i>) at the 2<sup>nd</sup> and 3<sup>rd</sup> periods. The biofilm extracts from <i>Bacillus cereus</i>, <i>Bacillus subtilis</i>, <i>Yersinia pseudotuberculosis</i> and <i>Staphylococcus aureus</i> also induced proinflammatory cytokines by HCAECs. By the experiments with IgG affinity chromatography, some of these serum KD-specific molecules bound to IgG.</p><p>Conclusions</p><p>We herein conclude that serum KD-specific molecules were mostly derived from biofilms and possessed molecular structures common to MAMPs from <i>Bacillus cereus, Bacillus subtilis</i>, <i>Yersinia pseudotuberculosis and Staphylococcus aureus</i>. Discovery of these KD-specific molecules might offer novel insight into the diagnosis and management of KD as well as its pathogenesis.</p></div

    LC-MS chromatograms of IgG sepharose-binding molecules.

    No full text
    <p>A. Representative LC-MS chromatograms of a IgG sepharose-binding molecule (m/z 1414.3) are shown in a KD patient and a DC control. TIC: Total ion current chromatograms, XIC: Extracted-ion chromatograms at m/z 1400–1500, and extracted-ion chromatograms at m/z 1414.3. (1) Human polyclonal IgG-conjugated sepharose 6 Fast (2) Inactivated CNBr Sepharose 4B control column. B. Binding of a KD-specific molecule to various affinity columns: Columns used are described in ONLINE METHODS. +: The binding quantities of a KD-specific molecule analyzed by LC-MS were equal or larger than those to human polyclonal IgG column, ±: smaller than 20% of those to human polyclonal IgG column, -: no binding. We performed the experiments 3 times.</p
    corecore