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Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features
Sphingolipids (SLs) serve as structural and signaling molecules in regulating various cellular events and growth. Given that SLs contain various bioactive species possessing distinct roles, quantitative analysis of sphingolipidome is essential for elucidating their differential requirement during de...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909964/ https://www.ncbi.nlm.nih.gov/pubmed/31853226 http://dx.doi.org/10.7150/ijbs.30499 |
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author | Cheng, Xiaoxiang Jiang, Xue Tam, Kin Yip Li, Gang Zheng, Jun Zhang, Hongjie |
author_facet | Cheng, Xiaoxiang Jiang, Xue Tam, Kin Yip Li, Gang Zheng, Jun Zhang, Hongjie |
author_sort | Cheng, Xiaoxiang |
collection | PubMed |
description | Sphingolipids (SLs) serve as structural and signaling molecules in regulating various cellular events and growth. Given that SLs contain various bioactive species possessing distinct roles, quantitative analysis of sphingolipidome is essential for elucidating their differential requirement during development. Herein we developed a comprehensive sphingolipidomic profiling approach using liquid chromatography-mass spectrometry coupled with multiple reaction monitoring mode (LC-MS-MRM). SL profiling of C. elegans revealed organism-specific, development-dependent and environment-driven metabolic features. We showed for the first time the presence of a series of sphingoid bases in C. elegans sphingolipid profiles, although only C17-sphingoid base is used for generating complex SLs. Moreover, we successfully resolved growth-, temperature- and nutrition-dependent SL profiles at both individual metabolite-level and network-level. Sphingolipidomic analysis uncovered significant SL composition changes throughout development, with SMs/GluCers ratios dramatically increasing from larva to adult stage whereas total sphingolipid levels exhibiting opposing trends. We also identified a temperature-dependent alteration in SMs/GluCers ratios, suggesting an organism-specific strategy for environmental adaptation. Finally, we found serine-biased GluCer increases between serine- versus alanine-supplemented worms. Our study builds a “reference” resource for future SL analysis in the worm, provides insights into natural variability and plasticity of eukaryotic multicellular sphingolipid composition and is highly valuable for investigating their functional significance. |
format | Online Article Text |
id | pubmed-6909964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-69099642019-12-18 Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features Cheng, Xiaoxiang Jiang, Xue Tam, Kin Yip Li, Gang Zheng, Jun Zhang, Hongjie Int J Biol Sci Research Paper Sphingolipids (SLs) serve as structural and signaling molecules in regulating various cellular events and growth. Given that SLs contain various bioactive species possessing distinct roles, quantitative analysis of sphingolipidome is essential for elucidating their differential requirement during development. Herein we developed a comprehensive sphingolipidomic profiling approach using liquid chromatography-mass spectrometry coupled with multiple reaction monitoring mode (LC-MS-MRM). SL profiling of C. elegans revealed organism-specific, development-dependent and environment-driven metabolic features. We showed for the first time the presence of a series of sphingoid bases in C. elegans sphingolipid profiles, although only C17-sphingoid base is used for generating complex SLs. Moreover, we successfully resolved growth-, temperature- and nutrition-dependent SL profiles at both individual metabolite-level and network-level. Sphingolipidomic analysis uncovered significant SL composition changes throughout development, with SMs/GluCers ratios dramatically increasing from larva to adult stage whereas total sphingolipid levels exhibiting opposing trends. We also identified a temperature-dependent alteration in SMs/GluCers ratios, suggesting an organism-specific strategy for environmental adaptation. Finally, we found serine-biased GluCer increases between serine- versus alanine-supplemented worms. Our study builds a “reference” resource for future SL analysis in the worm, provides insights into natural variability and plasticity of eukaryotic multicellular sphingolipid composition and is highly valuable for investigating their functional significance. Ivyspring International Publisher 2019-11-08 /pmc/articles/PMC6909964/ /pubmed/31853226 http://dx.doi.org/10.7150/ijbs.30499 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Cheng, Xiaoxiang Jiang, Xue Tam, Kin Yip Li, Gang Zheng, Jun Zhang, Hongjie Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features |
title | Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features |
title_full | Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features |
title_fullStr | Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features |
title_full_unstemmed | Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features |
title_short | Sphingolipidomic Analysis of C. elegans reveals Development- and Environment-dependent Metabolic Features |
title_sort | sphingolipidomic analysis of c. elegans reveals development- and environment-dependent metabolic features |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909964/ https://www.ncbi.nlm.nih.gov/pubmed/31853226 http://dx.doi.org/10.7150/ijbs.30499 |
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