25R,26-Hydroxycholesterol revisited: synthesis, metabolism, and biologic roles.

Abstract

The CYP27 gene is expressed in arterial endothelium, macrophages, and other tissues. The gene product generates sterol intermediates that function as ligands for nuclear receptors prior to their transport to the liver for metabolism, mostly to bile acids. Most attention has been given to 27-hydroxycholesterol as a ligand for LXR activated receptors and to chenodeoxycholic acid as a ligand for farnesoid X activated receptors (FXRs). Expression of the pathway in macrophages is essential for normal reverse cholesterol transport. Thus, ABC transporter activity is upregulated, which enhances cholesterol efflux. Absence of these mechanisms probably accounts for the accelerated atherosclerosis that occurs in cerebrotendinous xanthomatosis. Accumulation of 27-hydroxycholesterol in human atheroma is puzzling and may reflect low levels of oxysterol 7alpha-hydroxylase activity in human macrophages. The same enzyme determines the proportion of mono-, di-, and tri-hydroxy bile acids synthesized in the liver. Oxysterol 7alpha-hydroxylase deficiency is a molecular basis for cholestatic liver disease. Chenodeoxycholic acid, the major normal end product, downregulates expression of cholesterol 7alpha-hydroxylase via the FXR/short heterodimer protein nuclear receptor and thus limits total bile acid production. The challenge is to quantify in a physiologic setting the magnitude of the pathway in different tissues and to further evaluate the biologic roles of all the intermediates that may function as ligands for orphan nuclear receptors or via other regulatory mechanisms.

• Authors: Norman B Javitt
• Journal: Journal of lipid research (J Lipid Res) Vol. 43 Issue 5 Pg. 665-70 (May 2002) ISSN: 0022-2275 [Print] United States
• PMID: 11971935 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S., Review)

Chemical References

• Bile Acids and Salts
• Hydroxycholesterols
• 25-hydroxycholesterol
• Steroid Hydroxylases
• CYP27A1 protein, human
• Cholestanetriol 26-Monooxygenase

Topics

• Animals
• Bile Acids and Salts (biosynthesis)
• Cholestanetriol 26-Monooxygenase
• Fetus
• Humans
• Hydroxycholesterols (metabolism)
• Steroid Hydroxylases (genetics, metabolism)