AI Article Synopsis

  • The study utilizes NMR spectroscopy to analyze the metabolic activity of a single spheroid culture of human cancer cells, leveraging a micro-NMR platform for enhanced observation.
  • Changes in metabolite concentrations were tracked over time, revealing that these rates correlated with spheroid cell number and allowed for monitoring spheroids with roughly 2500 cells.
  • The research found that spheroids produced L-Lactic acid at a slower rate compared to monolayer cultures, and cells in spheroids exhibited consumption rather than production of certain metabolites like L-Alanine and L-Glutamine.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794408PMC
http://dx.doi.org/10.1038/s41598-020-79693-1DOI Listing

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