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Mass spectrometry imaging for in situ kinetic histochemistry
Tissues are composed of diverse cell subpopulations each with distinct metabolic characteristics that influence overall behavior. Unfortunately, traditional histopathology imaging techniques are ‘blind’ to the spatially ordered metabolic dynamics within tissue. While mass spectrometry imaging enable...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625901/ https://www.ncbi.nlm.nih.gov/pubmed/23584513 http://dx.doi.org/10.1038/srep01656 |
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author | Louie, Katherine B. Bowen, Benjamin P. McAlhany, Stephanie Huang, Yurong Price, John C. Mao, Jian-hua Hellerstein, Marc Northen, Trent R. |
author_facet | Louie, Katherine B. Bowen, Benjamin P. McAlhany, Stephanie Huang, Yurong Price, John C. Mao, Jian-hua Hellerstein, Marc Northen, Trent R. |
author_sort | Louie, Katherine B. |
collection | PubMed |
description | Tissues are composed of diverse cell subpopulations each with distinct metabolic characteristics that influence overall behavior. Unfortunately, traditional histopathology imaging techniques are ‘blind’ to the spatially ordered metabolic dynamics within tissue. While mass spectrometry imaging enables spatial mapping of molecular composition, resulting images are only a static snapshot in time of molecules involved in highly dynamic processes; kinetic information of flux through metabolic pathways is lacking. To address this limitation, we developed kinetic mass spectrometry imaging (kMSI), a novel technique integrating soft desorption/ionization mass spectrometry with clinically accepted in vivo metabolic labeling of tissue with deuterium to generate images of kinetic information of biological processes. Applied to a tumor, kMSI revealed heterogeneous spatial distributions of newly synthesized versus pre-existing lipids, with altered lipid synthesis patterns distinguishing region-specific intratumor subpopulations. Images also enabled identification and correlation of metabolic activity of specific lipids found in tumor regions of varying grade. |
format | Online Article Text |
id | pubmed-3625901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36259012013-04-15 Mass spectrometry imaging for in situ kinetic histochemistry Louie, Katherine B. Bowen, Benjamin P. McAlhany, Stephanie Huang, Yurong Price, John C. Mao, Jian-hua Hellerstein, Marc Northen, Trent R. Sci Rep Article Tissues are composed of diverse cell subpopulations each with distinct metabolic characteristics that influence overall behavior. Unfortunately, traditional histopathology imaging techniques are ‘blind’ to the spatially ordered metabolic dynamics within tissue. While mass spectrometry imaging enables spatial mapping of molecular composition, resulting images are only a static snapshot in time of molecules involved in highly dynamic processes; kinetic information of flux through metabolic pathways is lacking. To address this limitation, we developed kinetic mass spectrometry imaging (kMSI), a novel technique integrating soft desorption/ionization mass spectrometry with clinically accepted in vivo metabolic labeling of tissue with deuterium to generate images of kinetic information of biological processes. Applied to a tumor, kMSI revealed heterogeneous spatial distributions of newly synthesized versus pre-existing lipids, with altered lipid synthesis patterns distinguishing region-specific intratumor subpopulations. Images also enabled identification and correlation of metabolic activity of specific lipids found in tumor regions of varying grade. Nature Publishing Group 2013-04-15 /pmc/articles/PMC3625901/ /pubmed/23584513 http://dx.doi.org/10.1038/srep01656 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Louie, Katherine B. Bowen, Benjamin P. McAlhany, Stephanie Huang, Yurong Price, John C. Mao, Jian-hua Hellerstein, Marc Northen, Trent R. Mass spectrometry imaging for in situ kinetic histochemistry |
title | Mass spectrometry imaging for in situ kinetic histochemistry |
title_full | Mass spectrometry imaging for in situ kinetic histochemistry |
title_fullStr | Mass spectrometry imaging for in situ kinetic histochemistry |
title_full_unstemmed | Mass spectrometry imaging for in situ kinetic histochemistry |
title_short | Mass spectrometry imaging for in situ kinetic histochemistry |
title_sort | mass spectrometry imaging for in situ kinetic histochemistry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625901/ https://www.ncbi.nlm.nih.gov/pubmed/23584513 http://dx.doi.org/10.1038/srep01656 |
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