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Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism
Proceedings of the National Academy of Sciences, Volume: 117, Issue: 11, Pages: 5749 - 5760
Swansea University Authors: Eylan Yutuc , Roberto Angelini , David Skibinski , Owain Howell , Yuqin Wang , William Griffiths
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DOI (Published version): 10.1073/pnas.1917421117
Abstract
Dysregulated cholesterol metabolism is implicated in a number of neurological disorders. Many sterols, including cholesterol and its precursors and metabolites, are biologically active and important for proper brain function. However, spatial cholesterol metabolism in brain and the resulting sterol...
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ISSN: | 0027-8424 1091-6490 |
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Proceedings of the National Academy of Sciences
2020
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Many sterols, including cholesterol and its precursors and metabolites, are biologically active and important for proper brain function. However, spatial cholesterol metabolism in brain and the resulting sterol distributions are poorly defined. To better understand cholesterol metabolism in situ across the complex functional regions of brain, we have developed on-tissue enzyme-assisted derivatization in combination with microliquid extraction for surface analysis and liquid chromatography-mass spectrometry to locate sterols in tissue slices (10 µm) of mouse brain. The method provides sterolomic analysis at 400-µm spot diameter with a limit of quantification of 0.01 ng/mm2 It overcomes the limitations of previous mass spectrometry imaging techniques in analysis of low-abundance and difficult-to-ionize sterol molecules, allowing isomer differentiation and structure identification. Here we demonstrate the spatial distribution and quantification of multiple sterols involved in cholesterol metabolic pathways in wild-type and cholesterol 24S-hydroxylase knockout mouse brain. 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2020-09-21T15:52:46.1181247 v2 53792 2020-03-09 Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism 99332f073ce913a9b7d8b6441b17516d 0000-0001-9971-1950 Eylan Yutuc Eylan Yutuc true false 6405b7880498750d41c93c6ff89cff96 0000-0001-5136-5921 Roberto Angelini Roberto Angelini true false 328d16903f98c2b03a1cc64a7530322a 0000-0003-4077-6236 David Skibinski David Skibinski true false 58c995486fc93a242b987640b692db8c 0000-0003-2157-9157 Owain Howell Owain Howell true false c92729b58622f9fdf6a0e7d8f4ce5081 0000-0002-3063-3066 Yuqin Wang Yuqin Wang true false 3316b1d1b524be1831790933eed1c26e 0000-0002-4129-6616 William Griffiths William Griffiths true false 2020-03-09 BMS Dysregulated cholesterol metabolism is implicated in a number of neurological disorders. Many sterols, including cholesterol and its precursors and metabolites, are biologically active and important for proper brain function. However, spatial cholesterol metabolism in brain and the resulting sterol distributions are poorly defined. To better understand cholesterol metabolism in situ across the complex functional regions of brain, we have developed on-tissue enzyme-assisted derivatization in combination with microliquid extraction for surface analysis and liquid chromatography-mass spectrometry to locate sterols in tissue slices (10 µm) of mouse brain. The method provides sterolomic analysis at 400-µm spot diameter with a limit of quantification of 0.01 ng/mm2 It overcomes the limitations of previous mass spectrometry imaging techniques in analysis of low-abundance and difficult-to-ionize sterol molecules, allowing isomer differentiation and structure identification. Here we demonstrate the spatial distribution and quantification of multiple sterols involved in cholesterol metabolic pathways in wild-type and cholesterol 24S-hydroxylase knockout mouse brain. The technology described provides a powerful tool for future studies of spatial cholesterol metabolism in healthy and diseased tissues. Journal Article Proceedings of the National Academy of Sciences 117 11 5749 5760 Proceedings of the National Academy of Sciences 0027-8424 1091-6490 liquid chromatography-mass spectrometry, brain, cholesterol, 24Shydroxycholesterol, 24S,25-epoxycholesterol 17 3 2020 2020-03-17 10.1073/pnas.1917421117 COLLEGE NANME Biomedical Sciences COLLEGE CODE BMS Swansea University UKRI, BB/N015932/1 2020-09-21T15:52:46.1181247 2020-03-09T16:26:45.0375724 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Eylan Yutuc 0000-0001-9971-1950 1 Roberto Angelini 0000-0001-5136-5921 2 Mark Baumert 3 Natalia Mast 4 Irina Pikuleva 5 Jillian Newton 6 Malcolm R. Clench 7 David Skibinski 0000-0003-4077-6236 8 Owain Howell 0000-0003-2157-9157 9 Yuqin Wang 0000-0002-3063-3066 10 William Griffiths 0000-0002-4129-6616 11 53792__16817__111b974079a3460bb0927a4d5ca761be.pdf Yutuc PNAS 2020.pdf 2020-03-10T08:43:58.4799384 Output 2666851 application/pdf Version of Record true Distributed under the terms of a Creative Commons Attribution Licence 4.0 (CC-BY) true eng http://creativecommons.org/licenses/by/4.0/ |
title |
Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism |
spellingShingle |
Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism Eylan Yutuc Roberto Angelini David Skibinski Owain Howell Yuqin Wang William Griffiths |
title_short |
Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism |
title_full |
Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism |
title_fullStr |
Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism |
title_full_unstemmed |
Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism |
title_sort |
Localization of sterols and oxysterols in mouse brain reveals distinct spatial cholesterol metabolism |
author_id_str_mv |
99332f073ce913a9b7d8b6441b17516d 6405b7880498750d41c93c6ff89cff96 328d16903f98c2b03a1cc64a7530322a 58c995486fc93a242b987640b692db8c c92729b58622f9fdf6a0e7d8f4ce5081 3316b1d1b524be1831790933eed1c26e |
author_id_fullname_str_mv |
99332f073ce913a9b7d8b6441b17516d_***_Eylan Yutuc 6405b7880498750d41c93c6ff89cff96_***_Roberto Angelini 328d16903f98c2b03a1cc64a7530322a_***_David Skibinski 58c995486fc93a242b987640b692db8c_***_Owain Howell c92729b58622f9fdf6a0e7d8f4ce5081_***_Yuqin Wang 3316b1d1b524be1831790933eed1c26e_***_William Griffiths |
author |
Eylan Yutuc Roberto Angelini David Skibinski Owain Howell Yuqin Wang William Griffiths |
author2 |
Eylan Yutuc Roberto Angelini Mark Baumert Natalia Mast Irina Pikuleva Jillian Newton Malcolm R. Clench David Skibinski Owain Howell Yuqin Wang William Griffiths |
format |
Journal article |
container_title |
Proceedings of the National Academy of Sciences |
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117 |
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5749 |
publishDate |
2020 |
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Swansea University |
issn |
0027-8424 1091-6490 |
doi_str_mv |
10.1073/pnas.1917421117 |
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Proceedings of the National Academy of Sciences |
college_str |
Faculty of Medicine, Health and Life Sciences |
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Swansea University Medical School - Medicine{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Medicine |
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description |
Dysregulated cholesterol metabolism is implicated in a number of neurological disorders. Many sterols, including cholesterol and its precursors and metabolites, are biologically active and important for proper brain function. However, spatial cholesterol metabolism in brain and the resulting sterol distributions are poorly defined. To better understand cholesterol metabolism in situ across the complex functional regions of brain, we have developed on-tissue enzyme-assisted derivatization in combination with microliquid extraction for surface analysis and liquid chromatography-mass spectrometry to locate sterols in tissue slices (10 µm) of mouse brain. The method provides sterolomic analysis at 400-µm spot diameter with a limit of quantification of 0.01 ng/mm2 It overcomes the limitations of previous mass spectrometry imaging techniques in analysis of low-abundance and difficult-to-ionize sterol molecules, allowing isomer differentiation and structure identification. Here we demonstrate the spatial distribution and quantification of multiple sterols involved in cholesterol metabolic pathways in wild-type and cholesterol 24S-hydroxylase knockout mouse brain. The technology described provides a powerful tool for future studies of spatial cholesterol metabolism in healthy and diseased tissues. |
published_date |
2020-03-17T04:06:55Z |
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11.037581 |