Additional pathways of sterol metabolism: Evidence from analysis of Cyp27a1−/− mouse brain and plasma

Cytochrome P450 (CYP) 27A1 is a key enzyme in both the acidic and neutral pathways of bile acid biosynthesis accepting cholesterol and ring-hydroxylated sterols as substrates introducing a (25R)26-hydroxy and ultimately a (25R)26-acid group to the sterol side-chain. In human, mutations in the CYP27A...

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Veröffentlicht in:Biochimica et biophysica acta. Molecular and cell biology of lipids 2019-02, Vol.1864 (2), p.191-211
Hauptverfasser: Griffiths, William J., Crick, Peter J., Meljon, Anna, Theofilopoulos, Spyridon, Abdel-Khalik, Jonas, Yutuc, Eylan, Parker, Josie E., Kelly, Diane E., Kelly, Steven L., Arenas, Ernest, Wang, Yuqin
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container_issue 2
container_start_page 191
container_title Biochimica et biophysica acta. Molecular and cell biology of lipids
container_volume 1864
creator Griffiths, William J.
Crick, Peter J.
Meljon, Anna
Theofilopoulos, Spyridon
Abdel-Khalik, Jonas
Yutuc, Eylan
Parker, Josie E.
Kelly, Diane E.
Kelly, Steven L.
Arenas, Ernest
Wang, Yuqin
description Cytochrome P450 (CYP) 27A1 is a key enzyme in both the acidic and neutral pathways of bile acid biosynthesis accepting cholesterol and ring-hydroxylated sterols as substrates introducing a (25R)26-hydroxy and ultimately a (25R)26-acid group to the sterol side-chain. In human, mutations in the CYP27A1 gene are the cause of the autosomal recessive disease cerebrotendinous xanthomatosis (CTX). Surprisingly, Cyp27a1 knockout mice (Cyp27a1−/−) do not present a CTX phenotype despite generating a similar global pattern of sterols. Using liquid chromatography – mass spectrometry and exploiting a charge-tagging approach for oxysterol analysis we identified over 50 cholesterol metabolites and precursors in the brain and circulation of Cyp27a1−/− mice. Notably, we identified (25R)26,7α- and (25S)26,7α-dihydroxy epimers of oxysterols and cholestenoic acids, indicating the presence of an additional sterol 26-hydroxylase in mouse. Importantly, our analysis also revealed elevated levels of 7α-hydroxycholest-4-en-3-one, which we found increased the number of oculomotor neurons in primary mouse brain cultures. 7α-Hydroxycholest-4-en-3-one is a ligand for the pregnane X receptor (PXR), activation of which is known to up-regulate the expression of CYP3A11, which we confirm has sterol 26-hydroxylase activity. This can explain the formation of (25R)26,7α- and (25S)26,7α-dihydroxy epimers of oxysterols and cholestenoic acids; the acid with the former stereochemistry is a liver X receptor (LXR) ligand that increases the number of oculomotor neurons in primary brain cultures. We hereby suggest that a lack of a motor neuron phenotype in some CTX patients and Cyp27a1−/− mice may involve increased levels of 7α-hydroxycholest-4-en-3-one and activation PXR, as well as increased levels of sterol 26-hydroxylase and the production of neuroprotective sterols capable of activating LXR. [Display omitted] •Besides CYP27A1 an additional sterol 26-hydroxylase is present in mouse.•Sterol-acids are observed as 7α-hydroxy-(25R/S)26-acid epimers.•The (25S)26-acid is found in mouse brain of the CYP27A1−/− mouse.•The (25R)26-acid is found in brain of the wild type animal.•Both epimers are found in plasma of both genotypes.
doi_str_mv 10.1016/j.bbalip.2018.11.006
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In human, mutations in the CYP27A1 gene are the cause of the autosomal recessive disease cerebrotendinous xanthomatosis (CTX). Surprisingly, Cyp27a1 knockout mice (Cyp27a1−/−) do not present a CTX phenotype despite generating a similar global pattern of sterols. Using liquid chromatography – mass spectrometry and exploiting a charge-tagging approach for oxysterol analysis we identified over 50 cholesterol metabolites and precursors in the brain and circulation of Cyp27a1−/− mice. Notably, we identified (25R)26,7α- and (25S)26,7α-dihydroxy epimers of oxysterols and cholestenoic acids, indicating the presence of an additional sterol 26-hydroxylase in mouse. Importantly, our analysis also revealed elevated levels of 7α-hydroxycholest-4-en-3-one, which we found increased the number of oculomotor neurons in primary mouse brain cultures. 7α-Hydroxycholest-4-en-3-one is a ligand for the pregnane X receptor (PXR), activation of which is known to up-regulate the expression of CYP3A11, which we confirm has sterol 26-hydroxylase activity. This can explain the formation of (25R)26,7α- and (25S)26,7α-dihydroxy epimers of oxysterols and cholestenoic acids; the acid with the former stereochemistry is a liver X receptor (LXR) ligand that increases the number of oculomotor neurons in primary brain cultures. We hereby suggest that a lack of a motor neuron phenotype in some CTX patients and Cyp27a1−/− mice may involve increased levels of 7α-hydroxycholest-4-en-3-one and activation PXR, as well as increased levels of sterol 26-hydroxylase and the production of neuroprotective sterols capable of activating LXR. [Display omitted] •Besides CYP27A1 an additional sterol 26-hydroxylase is present in mouse.•Sterol-acids are observed as 7α-hydroxy-(25R/S)26-acid epimers.•The (25S)26-acid is found in mouse brain of the CYP27A1−/− mouse.•The (25R)26-acid is found in brain of the wild type animal.•Both epimers are found in plasma of both genotypes.</description><identifier>ISSN: 1388-1981</identifier><identifier>EISSN: 1879-2618</identifier><identifier>DOI: 10.1016/j.bbalip.2018.11.006</identifier><identifier>PMID: 30471425</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; bile acids ; Bile Acids and Salts - biosynthesis ; biosynthesis ; Brain ; Brain - metabolism ; Cerebrotendinous xanthomatosis ; Cholestanetriol 26-Monooxygenase - genetics ; Cholestanetriol 26-Monooxygenase - physiology ; Cholestenes - metabolism ; Cholestenoic acid ; Cholesterol - metabolism ; Chromatography, Liquid ; CYP27A1 ; cytochrome P-450 ; Cytochrome P-450 Enzyme System - metabolism ; enzyme activity ; enzymes ; genes ; humans ; Hydroxylation ; knockout mutants ; ligands ; Lipid Metabolism - physiology ; liquid chromatography ; liver ; Liver X Receptors - metabolism ; Male ; Mass spectrometry ; metabolites ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; motor neurons ; mutation ; Oxysterol ; oxysterols ; Oxysterols - metabolism ; patients ; phenotype ; Pregnane X Receptor - metabolism ; pregnanes ; stereochemistry ; Sterols - metabolism ; Tandem Mass Spectrometry ; Xanthomatosis, Cerebrotendinous</subject><ispartof>Biochimica et biophysica acta. Molecular and cell biology of lipids, 2019-02, Vol.1864 (2), p.191-211</ispartof><rights>2018 The Author(s)</rights><rights>Copyright © 2018 The Author(s). Published by Elsevier B.V. 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Molecular and cell biology of lipids</title><addtitle>Biochim Biophys Acta Mol Cell Biol Lipids</addtitle><description>Cytochrome P450 (CYP) 27A1 is a key enzyme in both the acidic and neutral pathways of bile acid biosynthesis accepting cholesterol and ring-hydroxylated sterols as substrates introducing a (25R)26-hydroxy and ultimately a (25R)26-acid group to the sterol side-chain. In human, mutations in the CYP27A1 gene are the cause of the autosomal recessive disease cerebrotendinous xanthomatosis (CTX). Surprisingly, Cyp27a1 knockout mice (Cyp27a1−/−) do not present a CTX phenotype despite generating a similar global pattern of sterols. Using liquid chromatography – mass spectrometry and exploiting a charge-tagging approach for oxysterol analysis we identified over 50 cholesterol metabolites and precursors in the brain and circulation of Cyp27a1−/− mice. Notably, we identified (25R)26,7α- and (25S)26,7α-dihydroxy epimers of oxysterols and cholestenoic acids, indicating the presence of an additional sterol 26-hydroxylase in mouse. Importantly, our analysis also revealed elevated levels of 7α-hydroxycholest-4-en-3-one, which we found increased the number of oculomotor neurons in primary mouse brain cultures. 7α-Hydroxycholest-4-en-3-one is a ligand for the pregnane X receptor (PXR), activation of which is known to up-regulate the expression of CYP3A11, which we confirm has sterol 26-hydroxylase activity. This can explain the formation of (25R)26,7α- and (25S)26,7α-dihydroxy epimers of oxysterols and cholestenoic acids; the acid with the former stereochemistry is a liver X receptor (LXR) ligand that increases the number of oculomotor neurons in primary brain cultures. We hereby suggest that a lack of a motor neuron phenotype in some CTX patients and Cyp27a1−/− mice may involve increased levels of 7α-hydroxycholest-4-en-3-one and activation PXR, as well as increased levels of sterol 26-hydroxylase and the production of neuroprotective sterols capable of activating LXR. [Display omitted] •Besides CYP27A1 an additional sterol 26-hydroxylase is present in mouse.•Sterol-acids are observed as 7α-hydroxy-(25R/S)26-acid epimers.•The (25S)26-acid is found in mouse brain of the CYP27A1−/− mouse.•The (25R)26-acid is found in brain of the wild type animal.•Both epimers are found in plasma of both genotypes.</description><subject>Animals</subject><subject>bile acids</subject><subject>Bile Acids and Salts - biosynthesis</subject><subject>biosynthesis</subject><subject>Brain</subject><subject>Brain - metabolism</subject><subject>Cerebrotendinous xanthomatosis</subject><subject>Cholestanetriol 26-Monooxygenase - genetics</subject><subject>Cholestanetriol 26-Monooxygenase - physiology</subject><subject>Cholestenes - metabolism</subject><subject>Cholestenoic acid</subject><subject>Cholesterol - metabolism</subject><subject>Chromatography, Liquid</subject><subject>CYP27A1</subject><subject>cytochrome P-450</subject><subject>Cytochrome P-450 Enzyme System - metabolism</subject><subject>enzyme activity</subject><subject>enzymes</subject><subject>genes</subject><subject>humans</subject><subject>Hydroxylation</subject><subject>knockout mutants</subject><subject>ligands</subject><subject>Lipid Metabolism - physiology</subject><subject>liquid chromatography</subject><subject>liver</subject><subject>Liver X Receptors - metabolism</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>metabolites</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>motor neurons</subject><subject>mutation</subject><subject>Oxysterol</subject><subject>oxysterols</subject><subject>Oxysterols - metabolism</subject><subject>patients</subject><subject>phenotype</subject><subject>Pregnane X Receptor - metabolism</subject><subject>pregnanes</subject><subject>stereochemistry</subject><subject>Sterols - metabolism</subject><subject>Tandem Mass Spectrometry</subject><subject>Xanthomatosis, Cerebrotendinous</subject><issn>1388-1981</issn><issn>1879-2618</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNqNks1u1DAQxyMEomXhDRDKkUtST_wZDkjVqnxIlbjA2XLsCfWSxMHObrVvwJlH5EnwskuhF8TBsuX5_ceemX9RPAdSAwFxsam7zgx-rhsCqgaoCREPinNQsq0aAephPlOlKmgVnBVPUtoQApxS_rg4o4RJYA0_L_ylc37xYTJDOZvl5tbsUxn6Mi0Yw1COuJguDD6Nr8qrnXc4WSz7GMbSZMU--V_wej830sCPb98v8irHsE1YdtH4KWOunAeTRvO0eNSbIeGz074qPr25-rh-V11_ePt-fXldWU7ZUjGBHJxQrCFOcGa5cFb1qjNCoSXc9iCpYpK21iGXDLlqm0a2xijeC8l6uiqqY950i_O203P0o4l7HYzXp6sv-YSaKdqCyPzrI58jIzqL0xLNcE92PzL5G_057LSgjTw0dFW8PCWI4esW06JHnywOg5kwd0I3oFpOgUnyHyiVTLagmoyyI2pjSClif_cjIPpgAL3RRwPogwE0gM4GyLIXf1dzJ_o98T_lYp7BzmPUyfrDWJ2PaBftgv_3Cz8BIS_Gag</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Griffiths, William J.</creator><creator>Crick, Peter J.</creator><creator>Meljon, Anna</creator><creator>Theofilopoulos, Spyridon</creator><creator>Abdel-Khalik, Jonas</creator><creator>Yutuc, Eylan</creator><creator>Parker, Josie E.</creator><creator>Kelly, Diane E.</creator><creator>Kelly, Steven L.</creator><creator>Arenas, Ernest</creator><creator>Wang, Yuqin</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>20190201</creationdate><title>Additional pathways of sterol metabolism: Evidence from analysis of Cyp27a1−/− mouse brain and plasma</title><author>Griffiths, William J. ; Crick, Peter J. ; Meljon, Anna ; Theofilopoulos, Spyridon ; Abdel-Khalik, Jonas ; Yutuc, Eylan ; Parker, Josie E. ; Kelly, Diane E. ; Kelly, Steven L. ; Arenas, Ernest ; Wang, Yuqin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-46e51d68420d654c56dc8f8ba68ec05cf17384739cde574e5892279aa85f674f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>bile acids</topic><topic>Bile Acids and Salts - biosynthesis</topic><topic>biosynthesis</topic><topic>Brain</topic><topic>Brain - metabolism</topic><topic>Cerebrotendinous xanthomatosis</topic><topic>Cholestanetriol 26-Monooxygenase - genetics</topic><topic>Cholestanetriol 26-Monooxygenase - physiology</topic><topic>Cholestenes - metabolism</topic><topic>Cholestenoic acid</topic><topic>Cholesterol - metabolism</topic><topic>Chromatography, Liquid</topic><topic>CYP27A1</topic><topic>cytochrome P-450</topic><topic>Cytochrome P-450 Enzyme System - metabolism</topic><topic>enzyme activity</topic><topic>enzymes</topic><topic>genes</topic><topic>humans</topic><topic>Hydroxylation</topic><topic>knockout mutants</topic><topic>ligands</topic><topic>Lipid Metabolism - physiology</topic><topic>liquid chromatography</topic><topic>liver</topic><topic>Liver X Receptors - metabolism</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>metabolites</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>motor neurons</topic><topic>mutation</topic><topic>Oxysterol</topic><topic>oxysterols</topic><topic>Oxysterols - metabolism</topic><topic>patients</topic><topic>phenotype</topic><topic>Pregnane X Receptor - metabolism</topic><topic>pregnanes</topic><topic>stereochemistry</topic><topic>Sterols - metabolism</topic><topic>Tandem Mass Spectrometry</topic><topic>Xanthomatosis, Cerebrotendinous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Griffiths, William J.</creatorcontrib><creatorcontrib>Crick, Peter J.</creatorcontrib><creatorcontrib>Meljon, Anna</creatorcontrib><creatorcontrib>Theofilopoulos, Spyridon</creatorcontrib><creatorcontrib>Abdel-Khalik, Jonas</creatorcontrib><creatorcontrib>Yutuc, Eylan</creatorcontrib><creatorcontrib>Parker, Josie E.</creatorcontrib><creatorcontrib>Kelly, Diane E.</creatorcontrib><creatorcontrib>Kelly, Steven L.</creatorcontrib><creatorcontrib>Arenas, Ernest</creatorcontrib><creatorcontrib>Wang, Yuqin</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Biochimica et biophysica acta. Molecular and cell biology of lipids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Griffiths, William J.</au><au>Crick, Peter J.</au><au>Meljon, Anna</au><au>Theofilopoulos, Spyridon</au><au>Abdel-Khalik, Jonas</au><au>Yutuc, Eylan</au><au>Parker, Josie E.</au><au>Kelly, Diane E.</au><au>Kelly, Steven L.</au><au>Arenas, Ernest</au><au>Wang, Yuqin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Additional pathways of sterol metabolism: Evidence from analysis of Cyp27a1−/− mouse brain and plasma</atitle><jtitle>Biochimica et biophysica acta. Molecular and cell biology of lipids</jtitle><addtitle>Biochim Biophys Acta Mol Cell Biol Lipids</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>1864</volume><issue>2</issue><spage>191</spage><epage>211</epage><pages>191-211</pages><issn>1388-1981</issn><eissn>1879-2618</eissn><abstract>Cytochrome P450 (CYP) 27A1 is a key enzyme in both the acidic and neutral pathways of bile acid biosynthesis accepting cholesterol and ring-hydroxylated sterols as substrates introducing a (25R)26-hydroxy and ultimately a (25R)26-acid group to the sterol side-chain. In human, mutations in the CYP27A1 gene are the cause of the autosomal recessive disease cerebrotendinous xanthomatosis (CTX). Surprisingly, Cyp27a1 knockout mice (Cyp27a1−/−) do not present a CTX phenotype despite generating a similar global pattern of sterols. Using liquid chromatography – mass spectrometry and exploiting a charge-tagging approach for oxysterol analysis we identified over 50 cholesterol metabolites and precursors in the brain and circulation of Cyp27a1−/− mice. Notably, we identified (25R)26,7α- and (25S)26,7α-dihydroxy epimers of oxysterols and cholestenoic acids, indicating the presence of an additional sterol 26-hydroxylase in mouse. Importantly, our analysis also revealed elevated levels of 7α-hydroxycholest-4-en-3-one, which we found increased the number of oculomotor neurons in primary mouse brain cultures. 7α-Hydroxycholest-4-en-3-one is a ligand for the pregnane X receptor (PXR), activation of which is known to up-regulate the expression of CYP3A11, which we confirm has sterol 26-hydroxylase activity. This can explain the formation of (25R)26,7α- and (25S)26,7α-dihydroxy epimers of oxysterols and cholestenoic acids; the acid with the former stereochemistry is a liver X receptor (LXR) ligand that increases the number of oculomotor neurons in primary brain cultures. We hereby suggest that a lack of a motor neuron phenotype in some CTX patients and Cyp27a1−/− mice may involve increased levels of 7α-hydroxycholest-4-en-3-one and activation PXR, as well as increased levels of sterol 26-hydroxylase and the production of neuroprotective sterols capable of activating LXR. [Display omitted] •Besides CYP27A1 an additional sterol 26-hydroxylase is present in mouse.•Sterol-acids are observed as 7α-hydroxy-(25R/S)26-acid epimers.•The (25S)26-acid is found in mouse brain of the CYP27A1−/− mouse.•The (25R)26-acid is found in brain of the wild type animal.•Both epimers are found in plasma of both genotypes.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30471425</pmid><doi>10.1016/j.bbalip.2018.11.006</doi><tpages>21</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1388-1981
ispartof Biochimica et biophysica acta. Molecular and cell biology of lipids, 2019-02, Vol.1864 (2), p.191-211
issn 1388-1981
1879-2618
language eng
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source MEDLINE; Elsevier ScienceDirect Journals; SWEPUB Freely available online
subjects Animals
bile acids
Bile Acids and Salts - biosynthesis
biosynthesis
Brain
Brain - metabolism
Cerebrotendinous xanthomatosis
Cholestanetriol 26-Monooxygenase - genetics
Cholestanetriol 26-Monooxygenase - physiology
Cholestenes - metabolism
Cholestenoic acid
Cholesterol - metabolism
Chromatography, Liquid
CYP27A1
cytochrome P-450
Cytochrome P-450 Enzyme System - metabolism
enzyme activity
enzymes
genes
humans
Hydroxylation
knockout mutants
ligands
Lipid Metabolism - physiology
liquid chromatography
liver
Liver X Receptors - metabolism
Male
Mass spectrometry
metabolites
Mice
Mice, Inbred C57BL
Mice, Knockout
motor neurons
mutation
Oxysterol
oxysterols
Oxysterols - metabolism
patients
phenotype
Pregnane X Receptor - metabolism
pregnanes
stereochemistry
Sterols - metabolism
Tandem Mass Spectrometry
Xanthomatosis, Cerebrotendinous
title Additional pathways of sterol metabolism: Evidence from analysis of Cyp27a1−/− mouse brain and plasma
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