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High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays
Methods to rapidly assess cell growth would be useful for many applications, including drug susceptibility testing, but current technologies have limited sensitivity or throughput. Here we present an approach to precisely and rapidly measure growth rates of many individual cells simultaneously. We f...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064867/ https://www.ncbi.nlm.nih.gov/pubmed/27598230 http://dx.doi.org/10.1038/nbt.3666 |
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author | Cermak, Nathan Olcum, Selim Delgado, Francisco Feijó Wasserman, Steven C. Payer, Kristofor R. Murakami, Mark Knudsen, Scott M. Kimmerling, Robert J. Stevens, Mark M. Kikuchi, Yuki Sandikci, Arzu Ogawa, Masaaki Agache, Vincent Baléras, François Weinstock, David M. Manalis, Scott R. |
author_facet | Cermak, Nathan Olcum, Selim Delgado, Francisco Feijó Wasserman, Steven C. Payer, Kristofor R. Murakami, Mark Knudsen, Scott M. Kimmerling, Robert J. Stevens, Mark M. Kikuchi, Yuki Sandikci, Arzu Ogawa, Masaaki Agache, Vincent Baléras, François Weinstock, David M. Manalis, Scott R. |
author_sort | Cermak, Nathan |
collection | PubMed |
description | Methods to rapidly assess cell growth would be useful for many applications, including drug susceptibility testing, but current technologies have limited sensitivity or throughput. Here we present an approach to precisely and rapidly measure growth rates of many individual cells simultaneously. We flow cells in suspension through a microfluidic channel with 10–12 resonant mass sensors distributed along its length, weighing each cell repeatedly over the 4–20 min it spends in the channel. Because multiple cells traverse the channel at the same time, we obtain growth rates for >60 cells/h with a resolution of 0.2 pg/h for mammalian cells and 0.02 pg/h for bacteria. We measure the growth of single lymphocytic cells, mouse and human T cells, primary human leukemia cells, yeast, Escherichia coli and Enterococcus faecalis. Our system reveals subpopulations of cells with divergent growth kinetics and enables assessment of cellular responses to antibiotics and antimicrobial peptides within minutes. |
format | Online Article Text |
id | pubmed-5064867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-50648672017-03-05 High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays Cermak, Nathan Olcum, Selim Delgado, Francisco Feijó Wasserman, Steven C. Payer, Kristofor R. Murakami, Mark Knudsen, Scott M. Kimmerling, Robert J. Stevens, Mark M. Kikuchi, Yuki Sandikci, Arzu Ogawa, Masaaki Agache, Vincent Baléras, François Weinstock, David M. Manalis, Scott R. Nat Biotechnol Article Methods to rapidly assess cell growth would be useful for many applications, including drug susceptibility testing, but current technologies have limited sensitivity or throughput. Here we present an approach to precisely and rapidly measure growth rates of many individual cells simultaneously. We flow cells in suspension through a microfluidic channel with 10–12 resonant mass sensors distributed along its length, weighing each cell repeatedly over the 4–20 min it spends in the channel. Because multiple cells traverse the channel at the same time, we obtain growth rates for >60 cells/h with a resolution of 0.2 pg/h for mammalian cells and 0.02 pg/h for bacteria. We measure the growth of single lymphocytic cells, mouse and human T cells, primary human leukemia cells, yeast, Escherichia coli and Enterococcus faecalis. Our system reveals subpopulations of cells with divergent growth kinetics and enables assessment of cellular responses to antibiotics and antimicrobial peptides within minutes. 2016-09-05 2016-10 /pmc/articles/PMC5064867/ /pubmed/27598230 http://dx.doi.org/10.1038/nbt.3666 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Cermak, Nathan Olcum, Selim Delgado, Francisco Feijó Wasserman, Steven C. Payer, Kristofor R. Murakami, Mark Knudsen, Scott M. Kimmerling, Robert J. Stevens, Mark M. Kikuchi, Yuki Sandikci, Arzu Ogawa, Masaaki Agache, Vincent Baléras, François Weinstock, David M. Manalis, Scott R. High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays |
title | High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays |
title_full | High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays |
title_fullStr | High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays |
title_full_unstemmed | High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays |
title_short | High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays |
title_sort | high-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064867/ https://www.ncbi.nlm.nih.gov/pubmed/27598230 http://dx.doi.org/10.1038/nbt.3666 |
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