Automation of the buccal micronucleus cytome assay using laser scanning cytometry.

Citation data:

Methods in cell biology, ISSN: 0091-679X, Vol: 102, Page: 321-39

Publication Year:
2011
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Citations 13
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Repository URL:
https://ro.ecu.edu.au/ecuworks2011/737; https://publications.csiro.au/rpr/pub?list=SEA&pid=csiro:EP104502
PMID:
21704845
DOI:
10.1016/b978-0-12-374912-3.00013-4
Author(s):
Leifert, Wayne R; Fran├žois, Maxime; Thomas, Philip; Luther, Ed; Holden, Elena; Fenech, Michael
Publisher(s):
Elsevier BV; Elsevier
Tags:
Biochemistry, Genetics and Molecular Biology; Medicine and Health Sciences
book chapter description
Laser scanning cytometry (LSC) can be used to quantify the fluorescence intensity or laser light loss (absorbance) of localized molecular targets within nuclear and cytoplasmic structures of cells while maintaining the morphological features of the examined tissue. It was aimed to develop an automated LSC protocol to study cellular and nuclear anomalies and DNA damage events in human buccal mucosal cells. Since the buccal micronucleus cytome assay has been used to measure biomarkers of DNA damage (micronuclei and/or nuclear buds), cytokinesis defects (binucleated cells), proliferative potential (basal cell frequency), and/or cell death (condensed chromatin, karyorrhexis, and pyknotic and karyolytic cells), the following automated LSC protocol describes scoring criteria for these same parameters using an automated imaging LSC. In this automated LSC assay, cells derived from the buccal mucosa were harvested from the inside of patient's mouths using a small-headed toothbrush. The cells were washed to remove any debris and/or bacteria, and a single-cell suspension prepared and applied to a microscope slide using a cytocentrifuge. Cells were fixed and stained with Feulgen and Light Green stain allowing both chromatic and fluorescent analysis to be undertaken simultaneously with the use of an LSC.