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Measurement of DNA content in single cells morphologically identified on smears.
Author(s) -
N Maruo,
T. Nakabo,
Motoharu Kondo
Publication year - 1986
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1177/34.10.3745905
Subject(s) - feulgen stain , dna , fluorescence , giemsa stain , nuclear dna , staining , microbiology and biotechnology , reagent , chemistry , bone marrow , biology , cell , pathology , chromatography , biochemistry , genetics , medicine , optics , gene , physics , mitochondrial dna
A method was developed for measuring the nuclear DNA content in single cells previously identified on a bone marrow smear stained by the Wright-Giemsa method. The smear was first photographed and the location of individual cells, identified by morphology, was recorded on a cell map. The smear was then bleached with 50% acid ethanol and absolute methanol, and re-stained by the Feulgen method in 0.05% pararosaniline Schiff's reagent (pH 2.3) at 7 degrees C for 10 min. Nuclear red fluorescence was observed and the intensity of this fluorescence was proportional to the amount of DNA after prior irradiation of smears with green light for 9 hr. The method is useful for measuring cell DNA content in heterogeneous cell populations when morphological cell identification is required.

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