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Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics
Interrogating polarized growth is technologically challenging due to extensive cellular branching and uncontrollable environmental conditions in conventional assays. Here we present a robust and high-performance microfluidic system that enables observations of polarized growth with enhanced temporal...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632079/ https://www.ncbi.nlm.nih.gov/pubmed/26530004 http://dx.doi.org/10.1038/srep16111 |
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author | Geng, Tao Bredeweg, Erin L. Szymanski, Craig J. Liu, Bingwen Baker, Scott E. Orr, Galya Evans, James E. Kelly, Ryan T. |
author_facet | Geng, Tao Bredeweg, Erin L. Szymanski, Craig J. Liu, Bingwen Baker, Scott E. Orr, Galya Evans, James E. Kelly, Ryan T. |
author_sort | Geng, Tao |
collection | PubMed |
description | Interrogating polarized growth is technologically challenging due to extensive cellular branching and uncontrollable environmental conditions in conventional assays. Here we present a robust and high-performance microfluidic system that enables observations of polarized growth with enhanced temporal and spatial control over prolonged periods. The system has built-in tunability and versatility to accommodate a variety of scientific applications requiring precisely controlled environments. Using the model filamentous fungus, Neurospora crassa, our microfluidic system enabled direct visualization and analysis of cellular heterogeneity in a clonal fungal cell population, nuclear distribution and dynamics at the subhyphal level, and quantitative dynamics of gene expression with single hyphal compartment resolution in response to carbon source starvation and exchange. Although the microfluidic device is demonstrated on filamentous fungi, the technology is immediately extensible to a wide array of other biosystems that exhibit similar polarized cell growth, with applications ranging from bioenergy production to human health. |
format | Online Article Text |
id | pubmed-4632079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46320792015-11-05 Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics Geng, Tao Bredeweg, Erin L. Szymanski, Craig J. Liu, Bingwen Baker, Scott E. Orr, Galya Evans, James E. Kelly, Ryan T. Sci Rep Article Interrogating polarized growth is technologically challenging due to extensive cellular branching and uncontrollable environmental conditions in conventional assays. Here we present a robust and high-performance microfluidic system that enables observations of polarized growth with enhanced temporal and spatial control over prolonged periods. The system has built-in tunability and versatility to accommodate a variety of scientific applications requiring precisely controlled environments. Using the model filamentous fungus, Neurospora crassa, our microfluidic system enabled direct visualization and analysis of cellular heterogeneity in a clonal fungal cell population, nuclear distribution and dynamics at the subhyphal level, and quantitative dynamics of gene expression with single hyphal compartment resolution in response to carbon source starvation and exchange. Although the microfluidic device is demonstrated on filamentous fungi, the technology is immediately extensible to a wide array of other biosystems that exhibit similar polarized cell growth, with applications ranging from bioenergy production to human health. Nature Publishing Group 2015-11-04 /pmc/articles/PMC4632079/ /pubmed/26530004 http://dx.doi.org/10.1038/srep16111 Text en Copyright © 2015, 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 Geng, Tao Bredeweg, Erin L. Szymanski, Craig J. Liu, Bingwen Baker, Scott E. Orr, Galya Evans, James E. Kelly, Ryan T. Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics |
title | Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics |
title_full | Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics |
title_fullStr | Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics |
title_full_unstemmed | Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics |
title_short | Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics |
title_sort | compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632079/ https://www.ncbi.nlm.nih.gov/pubmed/26530004 http://dx.doi.org/10.1038/srep16111 |
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