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PMID: 8800553 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A fluorescence digital image microscopy system for quantifying relative cell numbers in tissue culture plates.

Cytometry ·Vol. 24 ·No. 3 ·1996-07-01 ·Pages 204-13

Proffitt RT, Tran JV, Reynolds CP

Abstract

Microwell tissue culture plates provide a convenient format for conducting cell growth and cellular cytotoxicity assays, but such assays often have a limited dynamic range. We have developed the digital imaging microscopy scanning system (DIM-SCAN), which is a semiautomated fluorescence digital imaging system for quantifying relative cell numbers in situ in a variety of tissue culture plate formats, especially 96-well plates. The system consists of an epifluorescence inverted microscope with a motorized stage, video camera, image intensifier, and an 80386 microcomputer with a PC-Vision digitizer. Turbo Pascal software controls the stage and scans the plate taking multiple images per well, calculates total fluorescence per well, provides for daily calibration, and configures easily for a variety of tissue culture plate formats. Thresholding of digital images is used to remove background fluorescence without rinsing. Using cells pretreated with fluorescein diacetate (FDA) and loaded into 96-well plates, linearity was seen over 3.0 logs of cell density (r = 0.996), with similar results in 6-well (r = 0.972), 24-well (r = 0.970), and 48-well plates (r = 0.981). For cells stained directly in plates with Hoechst 33342, linearity was observed over 2.7 logs of cell density (r = 0.975). In low-viability cultures stained with FDA in 96-well plates, excessive background fluorescence completely masked viable cells, but digital thresholding dramatically reduced background fluorescence, producing a linear response (r = 9.333) over 2.7 logs of cell density (from 264 cells/well to 1.35 x 10(5) cells/well). DIM-SCAN is a versatile system for quantifying total or viable cell numbers in tissue culture plates over a wide dynamic range.

MeSH Terms
Algorithms Cell Count Computers Databases, Factual Fluorescence Humans Microscopy, Fluorescence/instrumentation Microscopy, Video Signal Processing, Computer-Assisted/instrumentation Tumor Cells, Cultured
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Proffitt R T
Department of Pediatrics, Childrens Hospital of Los Angeles, CA 90027, USA. cpreynol@hsc.usc.edu
Tran J V
Reynolds C P
Article Info
Journal
Cytometry
Abbr.
Cytometry
ISSN
0196-4763
Published
1996-07-01
Pages
204-13
Language
English
Region
United States
NLM ID
8102328
Subset
IM
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