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Flow cytometric analysis of micronucleated reticulocytes: Time‐ and dose‐dependent response of known mutagens in mice, using multiple blood sampling
Author(s) -
De Boeck Marlies,
van der Leede Basjan,
Van Goethem Freddy,
De Smedt Ann,
Steemans Margino,
Lampo Ann,
Vanparys Philippe
Publication year - 2005
Publication title -
environmental and molecular mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1
H-Index - 87
eISSN - 1098-2280
pISSN - 0893-6692
DOI - 10.1002/em.20127
Subject(s) - micronucleus test , clastogen , flow cytometry , propidium iodide , reticulocyte , transferrin receptor , biology , microbiology and biotechnology , mutagen , micronucleus , andrology , chemistry , immunology , toxicity , carcinogen , transferrin , biochemistry , medicine , apoptosis , organic chemistry , programmed cell death , messenger rna , gene
According to the current Organization of Economic Cooperation and Development (OECD) and International Committee on Harmonization (ICH) guidelines for the mammalian erythrocyte micronucleus (MN) test, analysis of peripheral blood reticulocytes (RETs) for the presence of micronuclei can be performed using flow cytometry. The MicroFlow®PLUS method (Litron Laboratories, Rochester, NY) for MN analysis by flow cytometry is based on the binding of FITC‐labeled antibodies to the CD71 transferrin receptor of immature RETs, on parallel RNA degradation, and on propidium iodide staining of DNA present as micronuclei. The objective of this study was to assess the sensitivity of this flow cytometry method to detect time‐ and dose‐dependent induction of micronuclei in mouse peripheral blood RETs after treatment with nine chemical agents. Five known clastogens, two known aneugens, and two compounds previously reported to be inactive in the mouse bone marrow MN test were evaluated at three dose levels. Multiple blood sampling of the same animal before and at two time points after treatment was conducted. All known mutagens produced a dose‐dependent increase in micronucleated reticulocytes (MN‐RETs); the compounds previously shown to be inactive in the in vivo MN test were also negative using the present methodology. The highest frequency of MN‐RETs was observed at 48 hr after treatment, except for 5‐fluorouracil, which had its peak response at 72 hr. The results indicate that micronuclei can be measured by multiple blood sampling of the same animal before and after treatment without altering the sensitivity of the assay. The results confirm that the flow cytometric assessment of MN‐RETs in mouse peripheral blood using MicroFlow®PLUS is a sensitive method with high analysis throughput, and robust quality control. Environ. Mol. Mutagen., 2005. © 2005 Wiley‐Liss, Inc.