Literature DB >> 22127256

Assessment of GFP expression and viability using the tali image-based cytometer.

Krissy Remple1, Laurel Stone.   

Abstract

Single-cell and population information are commonly obtained either by flow cytometry or fluorescence microscopy. However, these two methods provide different information. Flow cytometry gives quantitative multi-parametric information about physical characteristics and staining or expression, but doesn't allow for visualization. Stand-alone fluorescence microscopy provides visual data, but doesn't allow for straightforward quantitative measurements(1). Image-based cytometry bridges the gap between these two methods, enabling the quick visualization and simultaneous quantitative analysis of thousands of cells in heterogeneous populations(2). Here, we present a method for performing cell viability and green fluorescent protein (GFP) expression assays using the Tali Image-Based Cytometer(3). The Tali instrument is a 3-channel (bright field, green fluorescence, red fluorescence) benchtop assay platform that offers several advantages over flow cytometry and fluorescence microscopy. The Tali cytometer is less expensive, takes up less bench space, requires less maintenance, and the work flow has been simplified so that the operation and analysis is much simpler and quicker. The Tali cytometer is capable of performing a range of suspension cell-based assays, including GFP and red fluorescent protein (RFP) expression, apoptosis(4-6) and cell viability analysis with propidium iodide (PI)(7-11). Here, we demonstrate the use of the Tali instrument in performing a cell viability assay in cells expressing GFP. GFP-transduced cells are stained using the Tali Viability Kit - Dead Cell Red. The cells are then pipetted into a Tali Cellular Analysis Slide and loaded into the cytometer. Bright field, red fluorescence and green fluorescence images are captured and analyzed using assay specific algorithms. Histograms are then generated to display cell size, PI fluorescence intensity, and GFP fluorescence intensity. These parameters can then be thresholded to home in on a specific cell population. A side-by side comparison of the Tali Image-Based Cytometer and traditional flow cytometry demonstrates that the two methods provide comparable data regarding cell viability and protein expression. However, the Tali instrument provides additional visual information about the cell population that cannot be obtained using a flow cytometer.

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Year:  2011        PMID: 22127256      PMCID: PMC3308625          DOI: 10.3791/3659

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  11 in total

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Journal:  Biotechniques       Date:  2002-03       Impact factor: 1.993

Review 2.  Detection of dead cells and measurement of cell killing by flow cytometry.

Authors:  M A King
Journal:  J Immunol Methods       Date:  2000-09-21       Impact factor: 2.303

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5.  High-efficiency expression gene cloning by flow cytometry.

Authors:  R Dell'Arciprete; M Stella; M Fornaro; R Ciccocioppo; M G Capri; A M Naglieri; S Alberti
Journal:  J Histochem Cytochem       Date:  1996-06       Impact factor: 2.479

6.  A rapid, quantitative and inexpensive method for detecting apoptosis by flow cytometry in transiently transfected cells.

Authors:  G M Lamm; P Steinlein; M Cotten; G Christofori
Journal:  Nucleic Acids Res       Date:  1997-12-01       Impact factor: 16.971

7.  Alternative fluorochromes to ethidium bromide for automated read out of cytotoxicity tests.

Authors:  H J Tanke; P W van der Linden; J Langerak
Journal:  J Immunol Methods       Date:  1982       Impact factor: 2.303

8.  Annexin V for flow cytometric detection of phosphatidylserine expression on B cells undergoing apoptosis.

Authors:  G Koopman; C P Reutelingsperger; G A Kuijten; R M Keehnen; S T Pals; M H van Oers
Journal:  Blood       Date:  1994-09-01       Impact factor: 22.113

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Authors:  K H Jones; D A Kniss
Journal:  J Histochem Cytochem       Date:  1987-01       Impact factor: 2.479

10.  A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V.

Authors:  I Vermes; C Haanen; H Steffens-Nakken; C Reutelingsperger
Journal:  J Immunol Methods       Date:  1995-07-17       Impact factor: 2.303

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