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High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity
One of the primary effector functions of immune cells is the killing of virus-infected or malignant cells in the body. Natural killer (NK) and CD8 effector T cells are specialized for this function. The gold standard for measuring such cell-mediated cytolysis has been the chromium release assay, in...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981259/ https://www.ncbi.nlm.nih.gov/pubmed/29695103 http://dx.doi.org/10.3390/cells7050035 |
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author | Welter, Anna Sundararaman, Srividya Li, Ruliang Zhang, Ting Karulin, Alexey Y. Lehmann, Alexander Naeem, Villian Roen, Diana R. Kuerten, Stefanie Lehmann, Paul V. |
author_facet | Welter, Anna Sundararaman, Srividya Li, Ruliang Zhang, Ting Karulin, Alexey Y. Lehmann, Alexander Naeem, Villian Roen, Diana R. Kuerten, Stefanie Lehmann, Paul V. |
author_sort | Welter, Anna |
collection | PubMed |
description | One of the primary effector functions of immune cells is the killing of virus-infected or malignant cells in the body. Natural killer (NK) and CD8 effector T cells are specialized for this function. The gold standard for measuring such cell-mediated cytolysis has been the chromium release assay, in which the leakage of the radioactive isotope from damaged target cells is being detected. Flow cytometry-based single cell analysis of target cells has recently been established as a non-radioactive alternative. Here we introduce a target cell visualization assay (TVA) that applies similar target cell staining approaches as used in flow cytometry but based on single cell computer image analysis. Two versions of TVA are described here. In one, the decrease in numbers of calcein-stained, i.e., viable, target cells is assessed. In the other, the CFSE/PI TVA, the increase in numbers of dead target cells is established in addition. TVA assays are shown to operate with the same sensitivity as standard chromium release assays, and, leaving data audit trails in form of scanned (raw), analyzed, and quality-controlled images, thus meeting requirements for measuring cell-mediated cytolysis in a regulated environment. |
format | Online Article Text |
id | pubmed-5981259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-59812592018-06-01 High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity Welter, Anna Sundararaman, Srividya Li, Ruliang Zhang, Ting Karulin, Alexey Y. Lehmann, Alexander Naeem, Villian Roen, Diana R. Kuerten, Stefanie Lehmann, Paul V. Cells Article One of the primary effector functions of immune cells is the killing of virus-infected or malignant cells in the body. Natural killer (NK) and CD8 effector T cells are specialized for this function. The gold standard for measuring such cell-mediated cytolysis has been the chromium release assay, in which the leakage of the radioactive isotope from damaged target cells is being detected. Flow cytometry-based single cell analysis of target cells has recently been established as a non-radioactive alternative. Here we introduce a target cell visualization assay (TVA) that applies similar target cell staining approaches as used in flow cytometry but based on single cell computer image analysis. Two versions of TVA are described here. In one, the decrease in numbers of calcein-stained, i.e., viable, target cells is assessed. In the other, the CFSE/PI TVA, the increase in numbers of dead target cells is established in addition. TVA assays are shown to operate with the same sensitivity as standard chromium release assays, and, leaving data audit trails in form of scanned (raw), analyzed, and quality-controlled images, thus meeting requirements for measuring cell-mediated cytolysis in a regulated environment. MDPI 2018-04-24 /pmc/articles/PMC5981259/ /pubmed/29695103 http://dx.doi.org/10.3390/cells7050035 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Welter, Anna Sundararaman, Srividya Li, Ruliang Zhang, Ting Karulin, Alexey Y. Lehmann, Alexander Naeem, Villian Roen, Diana R. Kuerten, Stefanie Lehmann, Paul V. High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity |
title | High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity |
title_full | High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity |
title_fullStr | High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity |
title_full_unstemmed | High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity |
title_short | High-Throughput GLP-Capable Target Cell Visualization Assay for Measuring Cell-Mediated Cytotoxicity |
title_sort | high-throughput glp-capable target cell visualization assay for measuring cell-mediated cytotoxicity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981259/ https://www.ncbi.nlm.nih.gov/pubmed/29695103 http://dx.doi.org/10.3390/cells7050035 |
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