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Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain

Aberrant sterol lipid metabolism is associated with physiological dysfunctions in the aging brain and aging-dependent disorders such as neurodegenerative diseases. There is an unmet demand to comprehensively profile sterol lipids spatially and temporally in different brain regions during aging. Here...

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Autores principales: Li, Tongzhou, Yin, Yandong, Zhou, Zhiwei, Qiu, Jiaqian, Liu, Wenbin, Zhang, Xueting, He, Kaiwen, Cai, Yuping, Zhu, Zheng-Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282640/
https://www.ncbi.nlm.nih.gov/pubmed/34267224
http://dx.doi.org/10.1038/s41467-021-24672-x
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author Li, Tongzhou
Yin, Yandong
Zhou, Zhiwei
Qiu, Jiaqian
Liu, Wenbin
Zhang, Xueting
He, Kaiwen
Cai, Yuping
Zhu, Zheng-Jiang
author_facet Li, Tongzhou
Yin, Yandong
Zhou, Zhiwei
Qiu, Jiaqian
Liu, Wenbin
Zhang, Xueting
He, Kaiwen
Cai, Yuping
Zhu, Zheng-Jiang
author_sort Li, Tongzhou
collection PubMed
description Aberrant sterol lipid metabolism is associated with physiological dysfunctions in the aging brain and aging-dependent disorders such as neurodegenerative diseases. There is an unmet demand to comprehensively profile sterol lipids spatially and temporally in different brain regions during aging. Here, we develop an ion mobility-mass spectrometry based four-dimensional sterolomics technology leveraged by a machine learning-empowered high-coverage library (>2000 sterol lipids) for accurate identification. We apply this four-dimensional technology to profile the spatially resolved landscapes of sterol lipids in ten functional regions of the mouse brain, and quantitatively uncover ~200 sterol lipids uniquely distributed in specific regions with concentrations spanning up to 8 orders of magnitude. Further spatial analysis pinpoints age-associated differences in region-specific sterol lipid metabolism, revealing changes in the numbers of altered sterol lipids, concentration variations, and age-dependent coregulation networks. These findings will contribute to our understanding of abnormal sterol lipid metabolism and its role in brain diseases.
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spelling pubmed-82826402021-07-23 Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain Li, Tongzhou Yin, Yandong Zhou, Zhiwei Qiu, Jiaqian Liu, Wenbin Zhang, Xueting He, Kaiwen Cai, Yuping Zhu, Zheng-Jiang Nat Commun Article Aberrant sterol lipid metabolism is associated with physiological dysfunctions in the aging brain and aging-dependent disorders such as neurodegenerative diseases. There is an unmet demand to comprehensively profile sterol lipids spatially and temporally in different brain regions during aging. Here, we develop an ion mobility-mass spectrometry based four-dimensional sterolomics technology leveraged by a machine learning-empowered high-coverage library (>2000 sterol lipids) for accurate identification. We apply this four-dimensional technology to profile the spatially resolved landscapes of sterol lipids in ten functional regions of the mouse brain, and quantitatively uncover ~200 sterol lipids uniquely distributed in specific regions with concentrations spanning up to 8 orders of magnitude. Further spatial analysis pinpoints age-associated differences in region-specific sterol lipid metabolism, revealing changes in the numbers of altered sterol lipids, concentration variations, and age-dependent coregulation networks. These findings will contribute to our understanding of abnormal sterol lipid metabolism and its role in brain diseases. Nature Publishing Group UK 2021-07-15 /pmc/articles/PMC8282640/ /pubmed/34267224 http://dx.doi.org/10.1038/s41467-021-24672-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Tongzhou
Yin, Yandong
Zhou, Zhiwei
Qiu, Jiaqian
Liu, Wenbin
Zhang, Xueting
He, Kaiwen
Cai, Yuping
Zhu, Zheng-Jiang
Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain
title Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain
title_full Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain
title_fullStr Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain
title_full_unstemmed Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain
title_short Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain
title_sort ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282640/
https://www.ncbi.nlm.nih.gov/pubmed/34267224
http://dx.doi.org/10.1038/s41467-021-24672-x
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