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Expression of the cellular prion protein affects posttransfusion recovery and survival of red blood cells in mice

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F15%3A10313286" target="_blank" >RIV/00216208:11110/15:10313286 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1111/trf.13190" target="_blank" >http://dx.doi.org/10.1111/trf.13190</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/trf.13190" target="_blank" >10.1111/trf.13190</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Expression of the cellular prion protein affects posttransfusion recovery and survival of red blood cells in mice

  • Original language description

    BACKGROUNDCellular prion protein (PrPC) is expressed on various cell types including red blood cells (RBCs). The PrPC plays a key role in the pathogenesis of prion diseases, but its physiologic function remains unclear. PrPC is expressed on CD34+ hematopoietic stem cells and its expression is regulated during blood cell differentiation including the erythroid line. STUDY DESIGN AND METHODSWe investigated the role of PrPC in RBC survival in circulation by transfusing a mix of biotin-labeled RBCs from wild-type (WT) and PrP knockout (KO) mice to groups of recipient mice (WT and KO). The proportion of biotinylated RBCs in peripheral blood was estimated by flow cytometry. RESULTSKO RBCs displayed a markedly higher first-day posttransfusion recovery but hada decreased survival in circulation when compared to WT RBCs. Similar results were obtained in all groups of transfused mice, irrespective of RBCs biotinylation level. In addition, we confirmed this finding in an analogous study using Tg

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GAP303%2F12%2F1791" target="_blank" >GAP303/12/1791: The role of proteinase-activated receptors in pathogenesis of prion diseases</a><br>

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Transfusion

  • ISSN

    0041-1132

  • e-ISSN

  • Volume of the periodical

    55

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

    2590-2596

  • UT code for WoS article

    000364876100010

  • EID of the result in the Scopus database

    2-s2.0-84947087470