The enzymes, regulation, and genetics of bile acid synthesis
- PMID: 12543708
- DOI: 10.1146/annurev.biochem.72.121801.161712
The enzymes, regulation, and genetics of bile acid synthesis
Abstract
The synthesis and excretion of bile acids comprise the major pathway of cholesterol catabolism in mammals. Synthesis provides a direct means of converting cholesterol, which is both hydrophobic and insoluble, into a water-soluble and readily excreted molecule, the bile acid. The biosynthetic steps that accomplish this transformation also confer detergent properties to the bile acid, which are exploited by the body to facilitate the secretion of cholesterol from the liver. This role in the elimination of cholesterol is counterbalanced by the ability of bile acids to solubilize dietary cholesterol and essential nutrients and to promote their delivery to the liver. The synthesis of a full complement of bile acids requires 17 enzymes. The expression of selected enzymes in the pathway is tightly regulated by nuclear hormone receptors and other transcription factors, which ensure a constant supply of bile acids in an ever changing metabolic environment. Inherited mutations that impair bile acid synthesis cause a spectrum of human disease; this ranges from liver failure in early childhood to progressive neuropathy in adults.
Similar articles
-
Nuclear receptors in cholesterol catabolism: molecular biology of the enterohepatic circulation of bile salts and its role in cholesterol homeostasis.J Lab Clin Med. 2003 Jul;142(1):7-20. doi: 10.1016/S0022-2143(03)00088-X. J Lab Clin Med. 2003. PMID: 12878981 Review.
-
Nuclear receptors. I. Nuclear receptors and bile acid homeostasis.Am J Physiol Gastrointest Liver Physiol. 2002 Jun;282(6):G926-31. doi: 10.1152/ajpgi.00044.2002. Am J Physiol Gastrointest Liver Physiol. 2002. PMID: 12016116 Review.
-
Bile acid regulation of hepatic physiology: III. Regulation of bile acid synthesis: past progress and future challenges.Am J Physiol Gastrointest Liver Physiol. 2003 Apr;284(4):G551-7. doi: 10.1152/ajpgi.00468.2002. Am J Physiol Gastrointest Liver Physiol. 2003. PMID: 12631556 Review.
-
Genetics of familial intrahepatic cholestasis syndromes.J Med Genet. 2005 Jun;42(6):449-63. doi: 10.1136/jmg.2004.026187. J Med Genet. 2005. PMID: 15937079 Free PMC article. Review.
-
Bile acid regulation of hepatic physiology: III. Bile acids and nuclear receptors.Am J Physiol Gastrointest Liver Physiol. 2003 Mar;284(3):G349-56. doi: 10.1152/ajpgi.00417.2002. Am J Physiol Gastrointest Liver Physiol. 2003. PMID: 12576301 Review.
Cited by
-
Intestinal microbiota drives cholestasis-induced specific hepatic gene expression patterns.Gut Microbes. 2021 Jan-Dec;13(1):1-20. doi: 10.1080/19490976.2021.1911534. Gut Microbes. 2021. PMID: 33847205 Free PMC article.
-
Gut microbiome metabolites as key actors in atherosclerosis co-depression disease.Front Microbiol. 2022 Nov 10;13:988643. doi: 10.3389/fmicb.2022.988643. eCollection 2022. Front Microbiol. 2022. PMID: 36439791 Free PMC article. Review.
-
Dual action of peroxisome proliferator-activated receptor alpha in perfluorodecanoic acid-induced hepatotoxicity.Arch Toxicol. 2017 Feb;91(2):897-907. doi: 10.1007/s00204-016-1779-7. Epub 2016 Jun 25. Arch Toxicol. 2017. PMID: 27344344 Free PMC article.
-
Bile acid sensitivity and in vivo virulence of clinical Clostridium difficile isolates.Anaerobe. 2016 Oct;41:32-36. doi: 10.1016/j.anaerobe.2016.05.010. Epub 2016 May 27. Anaerobe. 2016. PMID: 27241781 Free PMC article.
-
Isoxanthohumol, a hop-derived flavonoid, alters the metabolomics profile of mouse feces.Biosci Microbiota Food Health. 2020;39(3):100-108. doi: 10.12938/bmfh.2019-045. Epub 2020 Feb 21. Biosci Microbiota Food Health. 2020. PMID: 32775127 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases