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Red blood cells serve as intravascular carriers of myeloperoxidase

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F14%3A00061113" target="_blank" >RIV/00159816:_____/14:00061113 - isvavai.cz</a>

  • Alternative codes found

    RIV/68081707:_____/14:00431577

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.yjmcc.2014.06.009" target="_blank" >http://dx.doi.org/10.1016/j.yjmcc.2014.06.009</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.yjmcc.2014.06.009" target="_blank" >10.1016/j.yjmcc.2014.06.009</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Red blood cells serve as intravascular carriers of myeloperoxidase

  • Original language description

    Myeloperoxidase (MPO) is a heme enzyme abundantly expressed in polymorphonuclear neutrophils. MPO is enzymatically capable of catalyzing the generation of reactive oxygen species (ROS) and the consumption of nitric oxide (NO). Thus MPO has both potent microbicidal and, upon binding to the vessel wall, pro-inflammatory properties. Interestingly, MPO - a highly cationic protein - has been shown to bind to both endothelial cells and leukocyte membranes. Given the anionic surface charge of red blood cells,we investigated binding of MPO to erythrocytes. Red blood cells (RBCs) derived from patients with elevated MPO plasma levels showed significantly higher amounts of MPO by flow cytometry and ELISA than healthy controls. Heparin-induced MPO-release from patient-derived RBCs was significantly increased compared to controls. Ex vivo experiments revealed dose and time dependency for MPO-RBC binding, and immunofluorescence staining as well as confocal microscopy localized MPO-RBC interaction t

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FA - Cardiovascular diseases including cardio-surgery

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Molecular and Cellular Cardiology

  • ISSN

    0022-2828

  • e-ISSN

  • Volume of the periodical

    74

  • Issue of the periodical within the volume

    September

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    11

  • Pages from-to

    353-63

  • UT code for WoS article

    000340077900039

  • EID of the result in the Scopus database