Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans[S]

The ubiquity of lipids in biological structures and functions suggests that lipid metabolisms are highly regulated. However, current invasive techniques for lipid studies prevent characterization of the dynamic interactions between various lipid metabolism pathways. Here, we describe a noninvasive a...

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Main Authors: Thuc T. Le, Holli M. Duren, Mikhail N. Slipchenko, Chang-Deng Hu, Ji-Xin Cheng
Format: Article
Language:English
Published: Elsevier 2010-03-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520305253
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author Thuc T. Le
Holli M. Duren
Mikhail N. Slipchenko
Chang-Deng Hu
Ji-Xin Cheng
author_facet Thuc T. Le
Holli M. Duren
Mikhail N. Slipchenko
Chang-Deng Hu
Ji-Xin Cheng
author_sort Thuc T. Le
collection DOAJ
description The ubiquity of lipids in biological structures and functions suggests that lipid metabolisms are highly regulated. However, current invasive techniques for lipid studies prevent characterization of the dynamic interactions between various lipid metabolism pathways. Here, we describe a noninvasive approach to study lipid metabolisms using a multifunctional coherent anti-Stokes Raman scattering (CARS) microscope. Using living Caenorhabditis elegans as a model organism, we report label-free visualization of coexisting neutral and autofluorescent lipid species. We find that the relative expression level of neutral and autofluorescent lipid species can be used to assay the genotype-phenotype relationship of mutant C. elegans with deletions in the genes encoding lipid synthesis transcription factors, LDL receptors, transforming growth factor β receptors, lipid desaturation enzymes, and antioxidant enzymes. Furthermore, by coupling CARS with fingerprint confocal Raman analysis, we analyze the unsaturation level of lipids in wild-type and mutant C. elegans. Our study shows that complex genotype-phenotype relationships between lipid storage, peroxidation, and desaturation can be rapidly and quantitatively analyzed in a single living C. elegans.
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spelling doaj.art-21bef8dbbd1f45b0885c87b12419c85e2022-12-21T20:08:07ZengElsevierJournal of Lipid Research0022-22752010-03-01513672677Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans[S]Thuc T. Le0Holli M. Duren1Mikhail N. Slipchenko2Chang-Deng Hu3Ji-Xin Cheng4Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN 47907Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907To whom correspondence should be addressed; Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN 47907; Purdue Cancer Center, Purdue University, West Lafayette, IN 47907To whom correspondence should be addressed; Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907; Purdue Cancer Center, Purdue University, West Lafayette, IN 47907; Department of Chemistry, Purdue University, West Lafayette, IN 47907The ubiquity of lipids in biological structures and functions suggests that lipid metabolisms are highly regulated. However, current invasive techniques for lipid studies prevent characterization of the dynamic interactions between various lipid metabolism pathways. Here, we describe a noninvasive approach to study lipid metabolisms using a multifunctional coherent anti-Stokes Raman scattering (CARS) microscope. Using living Caenorhabditis elegans as a model organism, we report label-free visualization of coexisting neutral and autofluorescent lipid species. We find that the relative expression level of neutral and autofluorescent lipid species can be used to assay the genotype-phenotype relationship of mutant C. elegans with deletions in the genes encoding lipid synthesis transcription factors, LDL receptors, transforming growth factor β receptors, lipid desaturation enzymes, and antioxidant enzymes. Furthermore, by coupling CARS with fingerprint confocal Raman analysis, we analyze the unsaturation level of lipids in wild-type and mutant C. elegans. Our study shows that complex genotype-phenotype relationships between lipid storage, peroxidation, and desaturation can be rapidly and quantitatively analyzed in a single living C. elegans.http://www.sciencedirect.com/science/article/pii/S0022227520305253cholesterol synthesiscoherent anti-Stokes Raman scatteringlipid desaturationlabel-free imaginglipid storageperoxidation
spellingShingle Thuc T. Le
Holli M. Duren
Mikhail N. Slipchenko
Chang-Deng Hu
Ji-Xin Cheng
Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans[S]
Journal of Lipid Research
cholesterol synthesis
coherent anti-Stokes Raman scattering
lipid desaturation
label-free imaging
lipid storage
peroxidation
title Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans[S]
title_full Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans[S]
title_fullStr Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans[S]
title_full_unstemmed Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans[S]
title_short Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans[S]
title_sort label free quantitative analysis of lipid metabolism in living caenorhabditis elegans s
topic cholesterol synthesis
coherent anti-Stokes Raman scattering
lipid desaturation
label-free imaging
lipid storage
peroxidation
url http://www.sciencedirect.com/science/article/pii/S0022227520305253
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