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@article{223212,
author = {Kozubek, Michal and Kozubek, Stanislav and Lukášová, Emilie and Marečková, Andrea and Bártová, Eva and Skalníková, Magdalena and Jergová, Adriana},
article_location = {New York},
article_number = {4},
keywords = {fluorescence in situ hybridization; interphase nuclei; fluorescence microscopy; automated microscopy; image analysis; 3-D analysis; high-resolution cytometry},
language = {eng},
issn = {0196-4763},
journal = {Cytometry},
title = {High-resolution cytometry of FISH dots in interphase cell nuclei},
volume = {36},
year = {1999}
}
TY - JOUR
ID - 223212
AU - Kozubek, Michal - Kozubek, Stanislav - Lukášová, Emilie - Marečková, Andrea - Bártová, Eva - Skalníková, Magdalena - Jergová, Adriana
PY - 1999
TI - High-resolution cytometry of FISH dots in interphase cell nuclei
JF - Cytometry
VL - 36
IS - 4
SP - 279
EP - 279
PB - International Society for Analytical Cyt
SN - 01964763
KW - fluorescence in situ hybridization
KW - interphase nuclei
KW - fluorescence microscopy
KW - automated microscopy
KW - image analysis
KW - 3-D analysis
KW - high-resolution cytometry
N2 - Background. Flow cytometry (FCM) and laser scanning cytometry (LSCM) provide indispensable tools for measuring large number of cells with low resolution. Confocal microscopy, on the other hand, is used for measuring small number of cells with high resolution. In this paper, we present a reasonable compromise between the two extremes. Methods. We have developed a completely automated, high-resolution system (high-resolution cytometer, HRCM) capable of analyzing microscope slides with FISH-stained interphase nuclei in 2-D as well as in 3-D using a fully motorized epi-fluorescence microscope and a cooled digital CCD camera fully controlled by a high-performance computer which performs both acquisition and related on-line image analysis. The images of different dyes are acquired sequentially using highly-specific filters and superimposed in computer memory. For each nucleus and each hybridization dot, user-selected attributes (such as position, size, intensity, etc.) are computed off-line using another processor or computer connected with a network. Results. Using HRCM, it is possible to analyze multi-color preparations including UV-excited dyes as well as repeatedly hybridized preparations re-acquiring individual nuclei. The speed of the acquisition and analysis is about 50 nuclei per minute in 2-D and 1 nucleus per minute in 3-D but depends on the density of nuclei on the slide; the precision of the lateral and axial measurements is approximately 100 nm. Conclusions. Thus, using overnight acquisition, quantities comparable to those of FCM or LSCM measurements can be analyzed with an accuracy comparable to confocal microscopy. HRCM is suitable for a number of clinical and scientific tasks: routine diagnostics, follow-up of therapy, studies of chromatin structure and many other different aspects of cell research.
ER -
KOZUBEK, Michal, Stanislav KOZUBEK, Emilie LUKÁŠOVÁ, Andrea MAREČKOVÁ, Eva BÁRTOVÁ, Magdalena SKALNÍKOVÁ and Adriana JERGOVÁ. High-resolution cytometry of FISH dots in interphase cell nuclei. \textit{Cytometry}. New York: International Society for Analytical Cyt, 1999, vol.~36, No~4, p.~279-293. ISSN~0196-4763.
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