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An Automated High-throughput Array Microscope for Cancer Cell Mechanics
Changes in cellular mechanical properties correlate with the progression of metastatic cancer along the epithelial-to-mesenchymal transition (EMT). Few high-throughput methodologies exist that measure cell compliance, which can be used to understand the impact of genetic alterations or to screen the...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893602/ https://www.ncbi.nlm.nih.gov/pubmed/27265611 http://dx.doi.org/10.1038/srep27371 |
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author | Cribb, Jeremy A. Osborne, Lukas D. Beicker, Kellie Psioda, Matthew Chen, Jian O’Brien, E. Timothy Taylor II, Russell M. Vicci, Leandra Hsiao, Joe Ping-Lin Shao, Chong Falvo, Michael Ibrahim, Joseph G. Wood, Kris C. Blobe, Gerard C. Superfine, Richard |
author_facet | Cribb, Jeremy A. Osborne, Lukas D. Beicker, Kellie Psioda, Matthew Chen, Jian O’Brien, E. Timothy Taylor II, Russell M. Vicci, Leandra Hsiao, Joe Ping-Lin Shao, Chong Falvo, Michael Ibrahim, Joseph G. Wood, Kris C. Blobe, Gerard C. Superfine, Richard |
author_sort | Cribb, Jeremy A. |
collection | PubMed |
description | Changes in cellular mechanical properties correlate with the progression of metastatic cancer along the epithelial-to-mesenchymal transition (EMT). Few high-throughput methodologies exist that measure cell compliance, which can be used to understand the impact of genetic alterations or to screen the efficacy of chemotherapeutic agents. We have developed a novel array high-throughput microscope (AHTM) system that combines the convenience of the standard 96-well plate with the ability to image cultured cells and membrane-bound microbeads in twelve independently-focusing channels simultaneously, visiting all wells in eight steps. We use the AHTM and passive bead rheology techniques to determine the relative compliance of human pancreatic ductal epithelial (HPDE) cells, h-TERT transformed HPDE cells (HPNE), and four gain-of-function constructs related to EMT. The AHTM found HPNE, H-ras, Myr-AKT, and Bcl2 transfected cells more compliant relative to controls, consistent with parallel tests using atomic force microscopy and invasion assays, proving the AHTM capable of screening for changes in mechanical phenotype. |
format | Online Article Text |
id | pubmed-4893602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48936022016-06-10 An Automated High-throughput Array Microscope for Cancer Cell Mechanics Cribb, Jeremy A. Osborne, Lukas D. Beicker, Kellie Psioda, Matthew Chen, Jian O’Brien, E. Timothy Taylor II, Russell M. Vicci, Leandra Hsiao, Joe Ping-Lin Shao, Chong Falvo, Michael Ibrahim, Joseph G. Wood, Kris C. Blobe, Gerard C. Superfine, Richard Sci Rep Article Changes in cellular mechanical properties correlate with the progression of metastatic cancer along the epithelial-to-mesenchymal transition (EMT). Few high-throughput methodologies exist that measure cell compliance, which can be used to understand the impact of genetic alterations or to screen the efficacy of chemotherapeutic agents. We have developed a novel array high-throughput microscope (AHTM) system that combines the convenience of the standard 96-well plate with the ability to image cultured cells and membrane-bound microbeads in twelve independently-focusing channels simultaneously, visiting all wells in eight steps. We use the AHTM and passive bead rheology techniques to determine the relative compliance of human pancreatic ductal epithelial (HPDE) cells, h-TERT transformed HPDE cells (HPNE), and four gain-of-function constructs related to EMT. The AHTM found HPNE, H-ras, Myr-AKT, and Bcl2 transfected cells more compliant relative to controls, consistent with parallel tests using atomic force microscopy and invasion assays, proving the AHTM capable of screening for changes in mechanical phenotype. Nature Publishing Group 2016-06-06 /pmc/articles/PMC4893602/ /pubmed/27265611 http://dx.doi.org/10.1038/srep27371 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Cribb, Jeremy A. Osborne, Lukas D. Beicker, Kellie Psioda, Matthew Chen, Jian O’Brien, E. Timothy Taylor II, Russell M. Vicci, Leandra Hsiao, Joe Ping-Lin Shao, Chong Falvo, Michael Ibrahim, Joseph G. Wood, Kris C. Blobe, Gerard C. Superfine, Richard An Automated High-throughput Array Microscope for Cancer Cell Mechanics |
title | An Automated High-throughput Array Microscope for Cancer Cell Mechanics |
title_full | An Automated High-throughput Array Microscope for Cancer Cell Mechanics |
title_fullStr | An Automated High-throughput Array Microscope for Cancer Cell Mechanics |
title_full_unstemmed | An Automated High-throughput Array Microscope for Cancer Cell Mechanics |
title_short | An Automated High-throughput Array Microscope for Cancer Cell Mechanics |
title_sort | automated high-throughput array microscope for cancer cell mechanics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893602/ https://www.ncbi.nlm.nih.gov/pubmed/27265611 http://dx.doi.org/10.1038/srep27371 |
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