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Reticulated platelets interfere with flow cytometric reticulocyte counts
Author(s) -
IVORY K.,
SARRIA B.,
FAIRWEATHERTAIT S. J.,
HUGHES D. A.
Publication year - 2007
Publication title -
international journal of laboratory hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.705
H-Index - 55
eISSN - 1751-553X
pISSN - 1751-5521
DOI - 10.1111/j.1365-2257.2006.00881.x
Subject(s) - reticulocyte , platelet , flow cytometry , population , red cell , microbiology and biotechnology , biology , chemistry , immunology , biochemistry , medicine , rna , environmental health , gene
Summary As part of an iron absorption study, we needed to accurately count reticulocytes in the peripheral blood of healthy human volunteers before measuring their enrichment with stable iron isotopes given in an oral dose. Recent studies have suggested the usefulness of reticulocyte counting by flow cytometry, through a combination of differential light scatter and measurement of the stoichiometric binding of thiazole orange (TO) to RNA within the maturing erythrocyte. Using this method we set out to improve the precision of our quantitative analysis by counting more cells, as reticulocytes normally comprise <2% of the red cell population. To ensure exclusion of other cell types, we identified WBCs and platelets with CD16+CD45− allophycocyanin and CD61− phycoerythrin, respectively. After removal of CD16 + CD45 + TO + WBCs and CD61 + TO − platelets from analysis, the remaining cells were a combination of CD61 − TO − erythrocytes, CD61 − TO + reticulocytes and CD61 + TO + reticulated platelets. Reticulocyte counts were lower after exclusion of CD61 + TO + cells from analysis. They were similarly lower when erythrocyte precursors were positively identified through their glycophorin A expression and TO uptake. We conclude that it is necessary to exclude reticulated platelets from flow cytometric reticulocyte analysis.