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A practical method to determine the amount of tissue to analyze using laser scanning cytometry
Author(s) -
Wijsman John A.,
Obert Leslie A.,
Paulissen Jerome,
Garrido Rosario,
Toy Katherine A.,
Dunstan Robert W.
Publication year - 2007
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.20397
Subject(s) - cytometry , flow cytometry , laser scanning , laser , biomedical engineering , computer science , biology , microbiology and biotechnology , medicine , optics , physics
Background: Laser scanning cytometry (LSC) is a new technology similar to flow cytometry but generates data from analysis of successive microscopic fields. Unlike its use in other applications, LSC‐generated data are not random when used for tissue sections, but are dependent on the microanatomy of the tissue and the distribution and expression of the protein under investigation. For valid LSC analysis, the data generated requires the evaluation of a sufficient tissue area to ensure an accurate representation of expression within the tissue of interest. Methods: In this report, we describe a simple and common sense method for determining the area of tissue required for sound LSC analysis by tracking the variation in the measure of target expression with increasing number of fields until it approaches zero. Results: This approach was used to evaluate the expression of immunohistochemical markers with differing tissue distributions in liver (PMP70, CYP1A2, and Ki67 positive macrophages) and a colorectal adenocarcinoma (activated caspase‐3 positive cells), which exhibited diffuse, regional (centrilobular), random, and irregular distribution patterns respectively. Conclusions: Analyses of these markers demonstrated that the amount of tissue area required to reach a steady measure of a parameter increased with increasing variability of the tissue distribution. © 2007 International Society for Analytical Cytology