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Time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic NMR
We present a quantitative study of the metabolic activity of a single spheroid culture of human cancer cells. NMR (nuclear magnetic resonance) spectroscopy is an ideal tool for observation of live systems due to its non-invasive nature. However, limited sensitivity has so far hindered its applicatio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794408/ https://www.ncbi.nlm.nih.gov/pubmed/33420162 http://dx.doi.org/10.1038/s41598-020-79693-1 |
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author | Patra, Bishnubrata Sharma, Manvendra Hale, William Utz, Marcel |
author_facet | Patra, Bishnubrata Sharma, Manvendra Hale, William Utz, Marcel |
author_sort | Patra, Bishnubrata |
collection | PubMed |
description | We present a quantitative study of the metabolic activity of a single spheroid culture of human cancer cells. NMR (nuclear magnetic resonance) spectroscopy is an ideal tool for observation of live systems due to its non-invasive nature. However, limited sensitivity has so far hindered its application in microfluidic culture systems. We have used an optimised micro-NMR platform to observe metabolic changes from a single spheroid. NMR spectra were obtained by directly inserting microfluidic devices containing spheroids ranging from 150 [Formula: see text] m to 300 [Formula: see text] m in diameter in 2.5 [Formula: see text] L of culture medium into a dedicated NMR probe. Metabolite concentrations were found to change linearly with time, with rates approximately proportional to the number of cells in the spheroid. The results demonstrate that quantitative monitoring of a single spheroid with [Formula: see text] 2500 cells is possible. A change in spheroid size by 600 cells leads to a clearly detectable change in the l-Lactic acid production rate ([Formula: see text] ). The consumption of d-Glucose and production of l-Lactic acid were approximately 2.5 times slower in spheroids compared to monolayer culture of the same number of cells. Moreover, while cells in monolayer culture were found to produce l-Alanine and l-Glutamine, spheroids showed slight consumption in both cases. |
format | Online Article Text |
id | pubmed-7794408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77944082021-01-11 Time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic NMR Patra, Bishnubrata Sharma, Manvendra Hale, William Utz, Marcel Sci Rep Article We present a quantitative study of the metabolic activity of a single spheroid culture of human cancer cells. NMR (nuclear magnetic resonance) spectroscopy is an ideal tool for observation of live systems due to its non-invasive nature. However, limited sensitivity has so far hindered its application in microfluidic culture systems. We have used an optimised micro-NMR platform to observe metabolic changes from a single spheroid. NMR spectra were obtained by directly inserting microfluidic devices containing spheroids ranging from 150 [Formula: see text] m to 300 [Formula: see text] m in diameter in 2.5 [Formula: see text] L of culture medium into a dedicated NMR probe. Metabolite concentrations were found to change linearly with time, with rates approximately proportional to the number of cells in the spheroid. The results demonstrate that quantitative monitoring of a single spheroid with [Formula: see text] 2500 cells is possible. A change in spheroid size by 600 cells leads to a clearly detectable change in the l-Lactic acid production rate ([Formula: see text] ). The consumption of d-Glucose and production of l-Lactic acid were approximately 2.5 times slower in spheroids compared to monolayer culture of the same number of cells. Moreover, while cells in monolayer culture were found to produce l-Alanine and l-Glutamine, spheroids showed slight consumption in both cases. Nature Publishing Group UK 2021-01-08 /pmc/articles/PMC7794408/ /pubmed/33420162 http://dx.doi.org/10.1038/s41598-020-79693-1 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Patra, Bishnubrata Sharma, Manvendra Hale, William Utz, Marcel Time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic NMR |
title | Time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic NMR |
title_full | Time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic NMR |
title_fullStr | Time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic NMR |
title_full_unstemmed | Time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic NMR |
title_short | Time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic NMR |
title_sort | time-resolved non-invasive metabolomic monitoring of a single cancer spheroid by microfluidic nmr |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794408/ https://www.ncbi.nlm.nih.gov/pubmed/33420162 http://dx.doi.org/10.1038/s41598-020-79693-1 |
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