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On the regulatory importance of 27-hydroxycholesterol in mouse liver
Vise andre og tillknytning
2017 (engelsk)Inngår i: Journal of Steroid Biochemistry and Molecular Biology, ISSN 0960-0760, E-ISSN 1879-1220, Vol. 169, s. 10-21Artikkel, forskningsoversikt (Fagfellevurdert) Published
Abstract [en]

27-Hydroxycholesterol (27OH) is a strong suppressor of cholesterol synthesis and a weak activator of LXR in vitro. The regulatory importance of 27OH in vivo is controversial. Here we utilized male mice with increased levels of 27OH either due to increased production (CYP27A1 transgenic mice) or reduced metabolism (Cyp7b1-/- mice). We also used mice lacking 27OH due to a knockout of Cyp27a1. The latter mice were treated with cholic acid to compensate for reduced bile acid synthesis. The effects of the different levels of 27OH on Srebp- and other LXR-regulated genes in the liver were investigated. In the liver of CYP27tg mice we found a modest increase of the mRNA levels corresponding to the LXR target genes Cyp7b1 and Abca1. A number of other LXR-regulated genes were not affected. The effect on Abca1 mRNA was not seen in the liver of Cyp7b1-/- mice. There were little or no effects on cholesterol synthesis. In the liver of the Cyp27-/- mice treated with 0.025% cholic acid there was no significant effect of the knockout on the LXR target genes. In a previous work triple-knockout mice deficient in the biosynthesis of 24S-hydroxycholesterol, 25-hydroxycholesterol and 27OH were shown to have impaired response to dietary cholesterol, suggesting side-chain oxidized oxysterols to be mediators in cholesterol-induced effects on LXR target genes at a transcriptional level (Chen W. et al., Cell Metab. 5 (2007) 73-79). The hydroxylated oxysterol responsible for the effect was not defined. We show here that treatment of wildtype mice with dietary cholesterol under the same conditions as in the above study induced the LXR target genes Lpl, Abcg8 and Srebp1c in wild type mice but failed to activate the same genes in mice lacking 27-hydroxycholesterol due to a knockout of Cyp27. We failed to demonstrate the above effects at the protein level (Abcg8) or at the activity level (Lpl). The results suggest that 27OH is not an important regulator of Srebp- or LXR regulated genes under basal conditions in mouse liver. On the other hand 27OH appears to mediate cholesterol-induced effects on some LXR target genes at a transcriptional level under some in vivo conditions. 

sted, utgiver, år, opplag, sider
Elsevier, 2017. Vol. 169, s. 10-21
Emneord [en]
Cholesterol metabolism, Gene expression, Nuclear receptor, OXysterols, Cytochrome P-450, Cyp27-/- mice, Lipoprotein lipase, Abcg8, Srebp1c, Lxr
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Identifikatorer
URN: urn:nbn:se:umu:diva-136070DOI: 10.1016/j.jsbmb.2016.02.001ISI: 000401391300003PubMedID: 26851362Scopus ID: 2-s2.0-84959419016OAI: oai:DiVA.org:umu-136070DiVA, id: diva2:1110656
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Special Issue: SI

Tilgjengelig fra: 2017-06-16 Laget: 2017-06-16 Sist oppdatert: 2023-03-24bibliografisk kontrollert

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Joibari, Masoumeh MotamediMakoveichuk, ElenaOlivercrona, Gunilla

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