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Real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an IncuCyte(®) imaging system
Cancer immunotherapy is a rapidly advancing and viable approach to treating cancer along with more traditional forms of therapy. Real-time cell analysis technologies that examine the dynamic interactions between cancer cells and the cells of the immune system are becoming more important for assessme...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Journal of Biological Methods
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300428/ https://www.ncbi.nlm.nih.gov/pubmed/32577423 http://dx.doi.org/10.14440/jbm.2020.323 |
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author | Lanigan, Thomas M. Rasmussen, Stephanie M. Weber, Daniel P. Athukorala, Kalana S. Campbell, Phillip L. Fox, David A. Ruth, Jeffrey H. |
author_facet | Lanigan, Thomas M. Rasmussen, Stephanie M. Weber, Daniel P. Athukorala, Kalana S. Campbell, Phillip L. Fox, David A. Ruth, Jeffrey H. |
author_sort | Lanigan, Thomas M. |
collection | PubMed |
description | Cancer immunotherapy is a rapidly advancing and viable approach to treating cancer along with more traditional forms of therapy. Real-time cell analysis technologies that examine the dynamic interactions between cancer cells and the cells of the immune system are becoming more important for assessment of novel therapeutics. In this report, we use the IncuCyte(®) imaging system to study the killing potential of various immune cells on cancer cell lines. The IncuCyte(®) system tracks living cells, labeled by a red fluorescent protein, and cell death, as indicated by the caspase-3/7 reagent, which generates a green fluorescent signal upon activation of apoptotic pathways. Despite the power of this approach, obtaining commercially fluorescent cancer cell lines is expensive and limited in the range of cell lines that are available. To overcome this barrier, we developed an inexpensive method using a lentiviral construct expressing nuclear localized mKate2 red fluorescent protein to stably label cancer cells. We demonstrate that this method is effective in labeling a wide variety of cell lines, allowing for analyses of different cancers as well as different cell lines of the same type of cancer. |
format | Online Article Text |
id | pubmed-7300428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Journal of Biological Methods |
record_format | MEDLINE/PubMed |
spelling | pubmed-73004282020-06-22 Real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an IncuCyte(®) imaging system Lanigan, Thomas M. Rasmussen, Stephanie M. Weber, Daniel P. Athukorala, Kalana S. Campbell, Phillip L. Fox, David A. Ruth, Jeffrey H. J Biol Methods Article Cancer immunotherapy is a rapidly advancing and viable approach to treating cancer along with more traditional forms of therapy. Real-time cell analysis technologies that examine the dynamic interactions between cancer cells and the cells of the immune system are becoming more important for assessment of novel therapeutics. In this report, we use the IncuCyte(®) imaging system to study the killing potential of various immune cells on cancer cell lines. The IncuCyte(®) system tracks living cells, labeled by a red fluorescent protein, and cell death, as indicated by the caspase-3/7 reagent, which generates a green fluorescent signal upon activation of apoptotic pathways. Despite the power of this approach, obtaining commercially fluorescent cancer cell lines is expensive and limited in the range of cell lines that are available. To overcome this barrier, we developed an inexpensive method using a lentiviral construct expressing nuclear localized mKate2 red fluorescent protein to stably label cancer cells. We demonstrate that this method is effective in labeling a wide variety of cell lines, allowing for analyses of different cancers as well as different cell lines of the same type of cancer. Journal of Biological Methods 2020-06-12 /pmc/articles/PMC7300428/ /pubmed/32577423 http://dx.doi.org/10.14440/jbm.2020.323 Text en © 2013-2020 The Journal of Biological Methods, All rights reserved. http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License: http://creativecommons.org/licenses/by-nc-sa/4.0 |
spellingShingle | Article Lanigan, Thomas M. Rasmussen, Stephanie M. Weber, Daniel P. Athukorala, Kalana S. Campbell, Phillip L. Fox, David A. Ruth, Jeffrey H. Real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an IncuCyte(®) imaging system |
title | Real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an IncuCyte(®) imaging system |
title_full | Real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an IncuCyte(®) imaging system |
title_fullStr | Real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an IncuCyte(®) imaging system |
title_full_unstemmed | Real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an IncuCyte(®) imaging system |
title_short | Real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an IncuCyte(®) imaging system |
title_sort | real time visualization of cancer cell death, survival and proliferation using fluorochrome-transfected cells in an incucyte(®) imaging system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300428/ https://www.ncbi.nlm.nih.gov/pubmed/32577423 http://dx.doi.org/10.14440/jbm.2020.323 |
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