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dc.contributor.advisor
dc.contributor.author György, Bence
dc.contributor.author Pálóczi, Krisztina
dc.contributor.author Kovács, Alexandra
dc.contributor.author Barabás, Eszter
dc.contributor.author Bekő, Gabriella
dc.contributor.author Várnai, Katalin
dc.contributor.author Pállinger, Éva
dc.contributor.author Szabó-Taylor, Katalin
dc.contributor.author Szabó, Géza Tamás
dc.contributor.author Kiss, Attila
dc.contributor.author Falus, András
dc.contributor.author Buzás, Edit Irén
dc.date.accessioned 2016-08-15T08:22:26Z
dc.date.available 2016-08-15T08:22:26Z
dc.date.issued 2013
dc.identifier 84892365208
dc.identifier.citation pagination=285-292; journalVolume=133; journalIssueNumber=2; journalTitle=THROMBOSIS RESEARCH;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3631
dc.identifier.uri doi:10.1016/j.thromres.2013.11.010
dc.description.abstract INTRODUCTION: Recently extracellular vesicles (exosomes, microparticles also referred to as microvesicles and apoptotic bodies) have attracted substantial interest as potential biomarkers and therapeutic vehicles. However, analysis of microparticles in biological fluids is confounded by many factors such as the activation of cells in the blood collection tube that leads to in vitro vesiculation. In this study we aimed at identifying an anticoagulant that prevents in vitro vesiculation in blood plasma samples. MATERIALS AND METHODS: We compared the levels of platelet microparticles and non-platelet-derived microparticles in platelet-free plasma samples of healthy donors. Platelet-free plasma samples were isolated using different anticoagulant tubes, and were analyzed by flow cytometry and Zymuphen assay. The extent of in vitro vesiculation was compared in citrate and acid-citrate-dextrose (ACD) tubes. RESULTS: Agitation and storage of blood samples at 37 degrees C for 1hour induced a strong release of both platelet microparticles and non-platelet-derived microparticles. Strikingly, in vitro vesiculation related to blood sample handling and storage was prevented in samples in ACD tubes. Importantly, microparticle levels elevated in vivo remained detectable in ACD tubes. CONCLUSIONS: We propose the general use of the ACD tube instead of other conventional anticoagulant tubes for the assessment of plasma microparticles since it gives a more realistic picture of the in vivo levels of circulating microparticles and does not interfere with downstream protein or RNA analyses.
dc.relation.ispartof urn:issn:0049-3848
dc.title Improved circulating microparticle analysis in acid-citrate dextrose (ACD) anticoagulant tube.
dc.type Journal Article
dc.date.updated 2016-08-12T10:41:06Z
dc.language.rfc3066 en
dc.identifier.mtmt 2492494
dc.identifier.wos 000329572600028
dc.identifier.pubmed 24360116
dc.contributor.department SE/AOK/I/Laboratóriumi Medicina Intézet
dc.contributor.department SE/AOK/I/Genetikai, Sejt- és Immunbiológiai Intézet
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote : Jul 24.


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