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Marked upregulation of cholesterol 25-hydroxylase expression by lipopolysaccharide
Department of Laboratory Medicine, Karolinska Institutet, Karolinska University Hospital, Huddinge, Sweden .
Department of Clinical Sciences, Malmö University Hospital, Lund University, Sweden .
Department of Clinical Sciences, Malmö University Hospital, Lund University, Sweden .
Department of Medicine, Division of Infectious Diseases and Immunology, University of Massachusetts Medical School, Worcester, MA .
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2009 (Engelska)Ingår i: Journal of Lipid Research, ISSN 0022-2275, E-ISSN 1539-7262, Vol. 50, nr 11, s. 2258-2264Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

During screening of genes upregulated by lipopolysaccharide (LPS; endotoxin) treatment of bone marrow-derived mouse macrophages, it was unexpectedly found that cholesterol 25-hydroxylase (Ch25h) was strongly upregulated. Treatment of macrophages with 10 ng/ml of LPS for 2 h resulted in a 35-fold increase in the expression of Ch25h. In contrast, LPS treatment did not increase the expression of Cyp27a1 or Cyp7b1. The increased Ch25h expression was found to be independent of Myeloid differentiation protein 88 signaling but dependent on Toll-like receptor 4 signaling. LPS treatment of macrophages caused a 6- to 7-fold increase in cellular 25-hydroxycholesterol concentration. When macrophages were treated with increasing concentrations of 25-hydroxycholesterol, a dose-dependent release of CCL5 into the culture medium was observed. Intravenous injection of LPS in eight healthy volunteers resulted in an increase in plasma 25-hydroxycholesterol concentration. The possibility is discussed that 25-hydroxycholesterol may have a role in the inflammatory response, in addition to its more established role in the regulation of cholesterol homeostasis.

Ort, förlag, år, upplaga, sidor
2009. Vol. 50, nr 11, s. 2258-2264
Nyckelord [en]
25-hydroxycholesterol, oxysterols, endotoxin, inflammation, sepsis, macrophages
Identifikatorer
URN: urn:nbn:se:umu:diva-37217DOI: 10.1194/jlr.M900107-JLR200PubMedID: 19502589OAI: oai:DiVA.org:umu-37217DiVA, id: diva2:358403
Tillgänglig från: 2010-10-21 Skapad: 2010-10-21 Senast uppdaterad: 2018-06-08Bibliografiskt granskad

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