Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17488
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dc.contributor.authorAlkhatatbeh, Mohammad J-
dc.contributor.authorEnjeti, Anoop K-
dc.contributor.authorBaqar, Sara-
dc.contributor.authorEkinci, Elif I-
dc.contributor.authorLiu, Dorothy-
dc.contributor.authorThorne, Rick F-
dc.contributor.authorLincz, Lisa F-
dc.date2018-04-05-
dc.date.accessioned2018-04-22T23:56:47Z-
dc.date.available2018-04-22T23:56:47Z-
dc.date.issued2018-04-05-
dc.identifier.citationJournal of Circulating Biomarkers 2018; online first: 5 Aprilen_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/17488-
dc.description.abstractEnumeration of circulating microvesicles (MVs) by conventional flow cytometry is accomplished by the addition of a known amount of counting beads and calculated from the formula: MV/μl = (MV count/bead count) × final bead concentration. We sought to optimize each variable in the equation by determining the best parameters for detecting 'MV count' and examining the effects of different bead preparations and concentrations on the final calculation. Three commercially available bead preparations (TruCount, Flow-Count and CountBright) were tested, and MV detection on a BD FACSCanto was optimized for gating by either forward scatter (FSC) or side scatter (SSC); the results were compared by calculating different subsets of MV on a series of 74 typical patient plasma samples. The relationship between the number of beads added to each test and the number of beads counted by flow cytometry remained linear over a wide range of bead concentrations (R2 ≥ 0.997). However, TruCount beads produced the most consistent (concentration variation = 3.8%) calculated numbers of plasma CD41+/Annexin V+ MV, which were significantly higher from that calculated using either Flow-Count or CountBright (p < 0.001). The FACSCanto was able to resolve 0.5 μm beads by FSC and 0.16 μm beads by SSC, but there were significantly more background events using SSC compared with FSC (3113 vs. 470; p = 0.008). In general, sample analysis by SSC resulted in significantly higher numbers of MV (p < 0.0001) but was well correlated with enumeration by FSC for all MV subtypes (ρ = 0.62-0.89, p < 0.0001). We conclude that all counting beads provided linear results at concentrations ranging from 6 beads/μl to 100 beads/μl, but TruCount was the most consistent. Using SSC to gate MV events produced high background which negatively affected counting bead enumeration and overall MV calculations. Strategies to reduce SSC background should be employed in order to reliably use this technique.en_US
dc.language.isoeng-
dc.subjectFlow cytometryen_US
dc.subjectabsolute countingen_US
dc.subjectextracellular vesiclesen_US
dc.subjectmicroparticlesen_US
dc.subjectmicrovesicleen_US
dc.subjectscatteren_US
dc.subjectsubmicron particlesen_US
dc.titleStrategies for enumeration of circulating microvesicles on a conventional flow cytometer: Counting beads and scatter parameters.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Circulating Biomarkersen_US
dc.identifier.affiliationHaematology Unit, Calvary Mater Newcastle, New South Wales, Australiaen_US
dc.identifier.affiliationHunter Medical Research Institute, New Lambton, New South Wales, Australiaen_US
dc.identifier.affiliationFaculty of Health and Medicine, University of Newcastle, New South Wales, Australiaen_US
dc.identifier.affiliationPathology North Hunter, NSW Health Pathology, New South Wales, Australiaen_US
dc.identifier.affiliationDepartment of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan.en_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.doi10.1177/1849454418766966en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-1612-2382en_US
dc.identifier.orcid0000-0003-2372-395Xen_US
dc.identifier.pubmedid29662552-
dc.type.austinJournal Article-
local.name.researcherEkinci, Elif I
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptEndocrinology-
crisitem.author.deptEndocrinology-
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