Studies on sterol 27-hydroxylase (CYP27A1)
Author: Bahr, Sara von
Date: 2004-02-20
Location: Rum M63, Karolinska Universitetssjukhuset, Huddinge
Time: 10.00
Department: Institutionen för laboratoriemedicin / Department of Laboratory Medicine
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Thesis (959.2Kb)
Abstract
Human sterol 27-hydroxylase (CYP27A1) has been studied in the present thesis with focus on substrate specificity and possible role of the enzyme for prevention of accumulation of cholesterol and cholestanol in tissues. Attempts have been made to evaluate a metabolic pathway to bile acids in human primary hepatocytes that starts with a 27-hydroxylation of cholesterol catalyzed by CYP27A1. The first Swedish case of sterol 27-hydroxylase deficiency (Cerebrotendinous xanthomatosis, CTX) is described and the mutation in the CYP27A1 gene is defined.
Substrate specificity. Polar substrates were found to be 27-hydroxylated more efficiently than unpolar substrates by recombinant CYP27A1 or by cells overexpressing CYP27A1. A precursor to cholesterol, 7-dehydrocholesterol, was found to be a less efficient substrate for CYP27A1. Cholestanol, a 5a-saturated analogue to cholesterol, was found to be 27-hydroxylated by CYP27A1 at about the same rate as cholesterol. Cholestenone, a precursor to cholestanol, was found to be a highly efficient substrate for CYP27A1. The findings may be part of the explanation for the accumulation of cholestanol in patients with a sterol 27-hydroxylase deficiency (CTX). Cholestanol was also found to leave cultured cells at a slower rate than cholesterol, giving a partial explanation for its selective accumulation in CTX.
Possible role in cholesterol accumulation. Cholesterolosis is a condition with accumulation of cholesterol esters in the mucosa of the gallbladder. CYP27A1 mRNA, CYP27A1 protein and CYP27A1 enzyme activity were found to be present in both normal gall bladder mucosa and in cholesterolosis in similar amounts. The esterifying enzyme ACAT was found to be upregulated in cholesterolosis, probably secondarily to the high cholesterol levels. The conclusion of the study is that CYP27A1 does not seem to be a pathogenic factor in cholesterolosis. Levels of esterified 27OH-cholesterol, the product of CYP27A1, were markedly increased in cholesterolosis, probably as a secondary effect of the increased esterification. Human tendons were found to contain CYP27A1 and the ratio between 27OH-cholesterol and cholesterol was found the be increased, suggesting that a similar mechanism is operating in tendons as in cholesterolosis. The findings are of interest in relation to the preferential accumulation of cholesterol and cholestanol in tendons of patients with CTX.
Role of 27-hydroxylation of cholesterol as the first step in bile acid formation in human hepatocytes. Labelled 27OH-cholesterol was found to be converted into cholic acid and chenodeoxycholic acid considerably less efficiently than the corresponding conversion of labelled 7aOH-cholesterol. The latter oxysterol is formed in the rate-limiting sterp in the classical pathway from cholesterol into bile acids. The preferential product of the pathway starting with 27OH-cholesterol was found to be chenodeoxycholic acid. Due to the variable degree of conversion in different experiments, no firm conclusions could be drawn with respect to the relative role of the pathway starting with a 27-hydroxylation.
First Swedish case with sterol 27-hydroxylase deficiency A cholestatic infant boy who died from organ failure was found to have a nonsence mutation in exon 7 (G1234T, or E408stop) in the CYP27A1 gene, a mutation not previously described. Both parents, who were first cousins, were found to be heterozygous for the mutation. Together with an infection with cytomegalovirus, the lack of CYP27A1 may have contributed to the death of this patient.
The results of the studies emphasize the importance of CYP27A1 and are consistent with the suggested role of the enzyme in preventing accumulation of cholesterol in various tissues.
Substrate specificity. Polar substrates were found to be 27-hydroxylated more efficiently than unpolar substrates by recombinant CYP27A1 or by cells overexpressing CYP27A1. A precursor to cholesterol, 7-dehydrocholesterol, was found to be a less efficient substrate for CYP27A1. Cholestanol, a 5a-saturated analogue to cholesterol, was found to be 27-hydroxylated by CYP27A1 at about the same rate as cholesterol. Cholestenone, a precursor to cholestanol, was found to be a highly efficient substrate for CYP27A1. The findings may be part of the explanation for the accumulation of cholestanol in patients with a sterol 27-hydroxylase deficiency (CTX). Cholestanol was also found to leave cultured cells at a slower rate than cholesterol, giving a partial explanation for its selective accumulation in CTX.
Possible role in cholesterol accumulation. Cholesterolosis is a condition with accumulation of cholesterol esters in the mucosa of the gallbladder. CYP27A1 mRNA, CYP27A1 protein and CYP27A1 enzyme activity were found to be present in both normal gall bladder mucosa and in cholesterolosis in similar amounts. The esterifying enzyme ACAT was found to be upregulated in cholesterolosis, probably secondarily to the high cholesterol levels. The conclusion of the study is that CYP27A1 does not seem to be a pathogenic factor in cholesterolosis. Levels of esterified 27OH-cholesterol, the product of CYP27A1, were markedly increased in cholesterolosis, probably as a secondary effect of the increased esterification. Human tendons were found to contain CYP27A1 and the ratio between 27OH-cholesterol and cholesterol was found the be increased, suggesting that a similar mechanism is operating in tendons as in cholesterolosis. The findings are of interest in relation to the preferential accumulation of cholesterol and cholestanol in tendons of patients with CTX.
Role of 27-hydroxylation of cholesterol as the first step in bile acid formation in human hepatocytes. Labelled 27OH-cholesterol was found to be converted into cholic acid and chenodeoxycholic acid considerably less efficiently than the corresponding conversion of labelled 7aOH-cholesterol. The latter oxysterol is formed in the rate-limiting sterp in the classical pathway from cholesterol into bile acids. The preferential product of the pathway starting with 27OH-cholesterol was found to be chenodeoxycholic acid. Due to the variable degree of conversion in different experiments, no firm conclusions could be drawn with respect to the relative role of the pathway starting with a 27-hydroxylation.
First Swedish case with sterol 27-hydroxylase deficiency A cholestatic infant boy who died from organ failure was found to have a nonsence mutation in exon 7 (G1234T, or E408stop) in the CYP27A1 gene, a mutation not previously described. Both parents, who were first cousins, were found to be heterozygous for the mutation. Together with an infection with cytomegalovirus, the lack of CYP27A1 may have contributed to the death of this patient.
The results of the studies emphasize the importance of CYP27A1 and are consistent with the suggested role of the enzyme in preventing accumulation of cholesterol in various tissues.
List of papers:
I. Norlin M, von Bahr S, Bjorkhem I, Wikvall K (2003). On the substrate specificity of human CYP27A1: implications for bile acid and cholestanol formation. J Lipid Res. 44(8): 1515-22. Epub 2003 Jun 01
Pubmed
II. Bjorkhem I, Starck L, Andersson U, Lutjohann D, von Bahr S, Pikuleva I, Babiker A, Diczfalusy U (2001). Oxysterols in the circulation of patients with the Smith-Lemli-Opitz syndrome: abnormal levels of 24S- and 27-hydroxycholesterol. J Lipid Res. 42(3): 366-71.
Pubmed
III. von Bahr S, Movin T, Papadogiannakis N, Pikuleva I, Ronnow P, Diczfalusy U, Bjorkhem I (2002). Mechanism of accumulation of cholesterol and cholestanol in tendons and the role of sterol 27-hydroxylase (CYP27A1). Arterioscler Thromb Vasc Biol. 22(7): 1129-35.
Pubmed
IV. Stromsten A, von Bahr S, Bringman S, Saeki M, Sahlin S, Bjorkhem I, Einarsson C (2004). Studies on the mechanism of accumulation of cholesterol in the gallbladder mucosa. Evidence that sterol 27-hydroxylase is not a pathogenetic factor. J Hepatol. 40(1): 8-13.
Pubmed
V. von Bahr S, Bjorkhem I, van´t Hooft F, Alevelius G, Nemeth A, Sjovall J, Fischler B (2004). Mutation in the sterol 27-hydroxylase gene associated with fatal cholestasis in infancy. [Manuscript]
VI. von Bahr S, Ellis E, Andersson U, Dicfalusy U, Kylander C, Einarsson C, Bjorkhem I (2004). Studies on the acidic pathway for formation of bile acids in human primary hepatocytes. [Manuscript]
I. Norlin M, von Bahr S, Bjorkhem I, Wikvall K (2003). On the substrate specificity of human CYP27A1: implications for bile acid and cholestanol formation. J Lipid Res. 44(8): 1515-22. Epub 2003 Jun 01
Pubmed
II. Bjorkhem I, Starck L, Andersson U, Lutjohann D, von Bahr S, Pikuleva I, Babiker A, Diczfalusy U (2001). Oxysterols in the circulation of patients with the Smith-Lemli-Opitz syndrome: abnormal levels of 24S- and 27-hydroxycholesterol. J Lipid Res. 42(3): 366-71.
Pubmed
III. von Bahr S, Movin T, Papadogiannakis N, Pikuleva I, Ronnow P, Diczfalusy U, Bjorkhem I (2002). Mechanism of accumulation of cholesterol and cholestanol in tendons and the role of sterol 27-hydroxylase (CYP27A1). Arterioscler Thromb Vasc Biol. 22(7): 1129-35.
Pubmed
IV. Stromsten A, von Bahr S, Bringman S, Saeki M, Sahlin S, Bjorkhem I, Einarsson C (2004). Studies on the mechanism of accumulation of cholesterol in the gallbladder mucosa. Evidence that sterol 27-hydroxylase is not a pathogenetic factor. J Hepatol. 40(1): 8-13.
Pubmed
V. von Bahr S, Bjorkhem I, van´t Hooft F, Alevelius G, Nemeth A, Sjovall J, Fischler B (2004). Mutation in the sterol 27-hydroxylase gene associated with fatal cholestasis in infancy. [Manuscript]
VI. von Bahr S, Ellis E, Andersson U, Dicfalusy U, Kylander C, Einarsson C, Bjorkhem I (2004). Studies on the acidic pathway for formation of bile acids in human primary hepatocytes. [Manuscript]
Issue date: 2004-01-30
Rights:
Publication year: 2004
ISBN: 91-7349-824-6
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