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In Vivo Metabolic Fingerprinting of Neutral Lipids with Hyperspectral Stimulated Raman Scattering Microscopy

[Image: see text] Metabolic fingerprinting provides valuable information on the physiopathological states of cells and tissues. Traditional imaging mass spectrometry and magnetic resonance imaging are unable to probe the spatial-temporal dynamics of metabolites at the subcellular level due to either...

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Autores principales: Fu, Dan, Yu, Yong, Folick, Andrew, Currie, Erin, Farese, Robert V., Tsai, Tsung-Huang, Xie, Xiaoliang Sunney, Wang, Meng C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073829/
https://www.ncbi.nlm.nih.gov/pubmed/24869754
http://dx.doi.org/10.1021/ja504199s
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author Fu, Dan
Yu, Yong
Folick, Andrew
Currie, Erin
Farese, Robert V.
Tsai, Tsung-Huang
Xie, Xiaoliang Sunney
Wang, Meng C.
author_facet Fu, Dan
Yu, Yong
Folick, Andrew
Currie, Erin
Farese, Robert V.
Tsai, Tsung-Huang
Xie, Xiaoliang Sunney
Wang, Meng C.
author_sort Fu, Dan
collection PubMed
description [Image: see text] Metabolic fingerprinting provides valuable information on the physiopathological states of cells and tissues. Traditional imaging mass spectrometry and magnetic resonance imaging are unable to probe the spatial-temporal dynamics of metabolites at the subcellular level due to either lack of spatial resolution or inability to perform live cell imaging. Here we report a complementary metabolic imaging technique that is based on hyperspectral stimulated Raman scattering (hsSRS). We demonstrated the use of hsSRS imaging in quantifying two major neutral lipids: cholesteryl ester and triacylglycerol in cells and tissues. Our imaging results revealed previously unknown changes of lipid composition associated with obesity and steatohepatitis. We further used stable-isotope labeling to trace the metabolic dynamics of fatty acids in live cells and live Caenorhabditis elegans with hsSRS imaging. We found that unsaturated fatty acid has preferential uptake into lipid storage while saturated fatty acid exhibits toxicity in hepatic cells. Simultaneous metabolic fingerprinting of deuterium-labeled saturated and unsaturated fatty acids in living C. elegans revealed that there is a lack of interaction between the two, unlike previously hypothesized. Our findings provide new approaches for metabolic tracing of neutral lipids and their precursors in living cells and organisms, and could potentially serve as a general approach for metabolic fingerprinting of other metabolites.
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spelling pubmed-40738292015-05-28 In Vivo Metabolic Fingerprinting of Neutral Lipids with Hyperspectral Stimulated Raman Scattering Microscopy Fu, Dan Yu, Yong Folick, Andrew Currie, Erin Farese, Robert V. Tsai, Tsung-Huang Xie, Xiaoliang Sunney Wang, Meng C. J Am Chem Soc [Image: see text] Metabolic fingerprinting provides valuable information on the physiopathological states of cells and tissues. Traditional imaging mass spectrometry and magnetic resonance imaging are unable to probe the spatial-temporal dynamics of metabolites at the subcellular level due to either lack of spatial resolution or inability to perform live cell imaging. Here we report a complementary metabolic imaging technique that is based on hyperspectral stimulated Raman scattering (hsSRS). We demonstrated the use of hsSRS imaging in quantifying two major neutral lipids: cholesteryl ester and triacylglycerol in cells and tissues. Our imaging results revealed previously unknown changes of lipid composition associated with obesity and steatohepatitis. We further used stable-isotope labeling to trace the metabolic dynamics of fatty acids in live cells and live Caenorhabditis elegans with hsSRS imaging. We found that unsaturated fatty acid has preferential uptake into lipid storage while saturated fatty acid exhibits toxicity in hepatic cells. Simultaneous metabolic fingerprinting of deuterium-labeled saturated and unsaturated fatty acids in living C. elegans revealed that there is a lack of interaction between the two, unlike previously hypothesized. Our findings provide new approaches for metabolic tracing of neutral lipids and their precursors in living cells and organisms, and could potentially serve as a general approach for metabolic fingerprinting of other metabolites. American Chemical Society 2014-05-28 2014-06-18 /pmc/articles/PMC4073829/ /pubmed/24869754 http://dx.doi.org/10.1021/ja504199s Text en Copyright © 2014 American Chemical Society Open Access on 05/28/2015
spellingShingle Fu, Dan
Yu, Yong
Folick, Andrew
Currie, Erin
Farese, Robert V.
Tsai, Tsung-Huang
Xie, Xiaoliang Sunney
Wang, Meng C.
In Vivo Metabolic Fingerprinting of Neutral Lipids with Hyperspectral Stimulated Raman Scattering Microscopy
title In Vivo Metabolic Fingerprinting of Neutral Lipids with Hyperspectral Stimulated Raman Scattering Microscopy
title_full In Vivo Metabolic Fingerprinting of Neutral Lipids with Hyperspectral Stimulated Raman Scattering Microscopy
title_fullStr In Vivo Metabolic Fingerprinting of Neutral Lipids with Hyperspectral Stimulated Raman Scattering Microscopy
title_full_unstemmed In Vivo Metabolic Fingerprinting of Neutral Lipids with Hyperspectral Stimulated Raman Scattering Microscopy
title_short In Vivo Metabolic Fingerprinting of Neutral Lipids with Hyperspectral Stimulated Raman Scattering Microscopy
title_sort in vivo metabolic fingerprinting of neutral lipids with hyperspectral stimulated raman scattering microscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073829/
https://www.ncbi.nlm.nih.gov/pubmed/24869754
http://dx.doi.org/10.1021/ja504199s
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