词条 | CYP4F3 |
释义 |
FunctionThe cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids, fatty acids and other lipids. CYP4F3 actually encodes two splice-variants, CYP4F3A and CYP4F3B, of the cytochrome P450 superfamily of enzymes. The gene is part of a cluster of cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F8, is approximately 18 kb away.[3] Both variants localize on the endoplasmic reticulum and metabolize leukotriene B4 and very likely 5-hydroxyeicosatetraenoic acid, 5-oxo-eicosatetraenoic acid, and 12-hydroxyeicosatetraenoic acid by an omega oxidation reaction, i.e. by adding a hydroxyl residue to their terminal (i.e. C-20) carbon.[5] This addition starts the process of inactivating and degrading all of these well-known mediators of inflammation and/or allery.[6] CYP3FA is the major enzyme accomplishing these omega oxidations in leukocytes.[6] The hydroxylation-induced inactivation of these mediators, perhaps particularly of leukotriene B4, may underlie the proposed roles of these cytochromes in dampening inflammatory responses as well as the reported associations of certain CYP4F3 single nucleotide variants (SNPs) with human Krohn's disease (SNPs are designated Rs1290617[7] and rs1290620[8] and Celiac disease (rs1290622 and rs1290625).[4][9][10][10][11][12] CYP4F3A and/or CYP43B also omega oxidize arachidonic acid to 20-Hydroxyeicosatetraenoic acid (20-HETE) as well as epoxyeicosatrienoic acids (EETs) to 20-hydroxy-EETs.[6] 20-HETE regulates blood flow, vascularization, blood pressure, and kidney tubule absorption of ions in rodents and possibly humans;[4] it has also been proposed to be involved in regulating the growth of various types of human cancers (see 20-Hydroxyeicosatetraenoic acid#cancer). EETS have a similar set of regulatory functions but often act in a manner opposite to 20-HETE (see epoxyeicosatrienoic acid#cancer); since, however, the activities of the 20-HEETs have not been well-defined, the function of EET omega oxidation is unclear.[4] References1. ^{{cite journal | vauthors = Kikuta Y, Kusunose E, Endo K, Yamamoto S, Sogawa K, Fujii-Kuriyama Y, Kusunose M | title = A novel form of cytochrome P-450 family 4 in human polymorphonuclear leukocytes. cDNA cloning and expression of leukotriene B4 omega-hydroxylase | journal = The Journal of Biological Chemistry | volume = 268 | issue = 13 | pages = 9376–80 | date = May 1993 | pmid = 8486631 | pmc = | doi = }} 2. ^{{cite journal | vauthors = Kikuta Y, Kato M, Yamashita Y, Miyauchi Y, Tanaka K, Kamada N, Kusunose M | title = Human leukotriene B4 omega-hydroxylase (CYP4F3) gene: molecular cloning and chromosomal localization | journal = DNA and Cell Biology | volume = 17 | issue = 3 | pages = 221–30 | date = March 1998 | pmid = 9539102 | pmc = | doi = 10.1089/dna.1998.17.221 }} 3. ^1 {{cite web | title = Entrez Gene: CYP4F3 cytochrome P450, family 4, subfamily F, polypeptide 3| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4051| accessdate = }} 4. ^1 2 3 {{cite journal | vauthors = Corcos L, Lucas D, Le Jossic-Corcos C, Dréano Y, Simon B, Plée-Gautier E, Amet Y, Salaün JP | title = Human cytochrome P450 4F3: structure, functions, and prospects | journal = Drug Metabolism and Drug Interactions | volume = 27 | issue = 2 | pages = 63–71 | year = 2012 | pmid = 22706230 | doi = 10.1515/dmdi-2011-0037 }} 5. ^{{cite journal | vauthors = Powell WS, Rokach J | title = Biosynthesis, biological effects, and receptors of hydroxyeicosatetraenoic acids (HETEs) and oxoeicosatetraenoic acids (oxo-ETEs) derived from arachidonic acid | journal = Biochimica et Biophysica Acta | volume = 1851 | issue = 4 | pages = 340–55 | date = April 2015 | pmid = 25449650 | doi = 10.1016/j.bbalip.2014.10.008 }} 6. ^1 2 {{cite journal | vauthors = Johnson AL, Edson KZ, Totah RA, Rettie AE | title = Cytochrome P450 ω-Hydroxylases in Inflammation and Cancer | journal = Advances in Pharmacology | volume = 74 | pages = 223–62 | year = 2015 | pmid = 26233909 | doi = 10.1016/bs.apha.2015.05.002 | pmc=4667791}} 7. ^{{cite web | url = http://www.snpedia.com/index.php/Rs1290617 | title = Rs1290617 | format = | work = SNPedia | accessdate = }} 8. ^{{cite web | url = https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=1290620 | title = Reference SNP (refSNP) Cluster Report: rs1290620 | format = | work = | accessdate = }} 9. ^{{cite journal | vauthors = Curley CR, Monsuur AJ, Wapenaar MC, Rioux JD, Wijmenga C | title = A functional candidate screen for coeliac disease genes | journal = European Journal of Human Genetics | volume = 14 | issue = 11 | pages = 1215–22 | year = 2006 | pmid = 16835590 | doi = 10.1038/sj.ejhg.5201687 }} 10. ^1 {{cite journal | vauthors = Costea I, Mack DR, Lemaitre RN, Israel D, Marcil V, Ahmad A, Amre DK | title = Interactions between the dietary polyunsaturated fatty acid ratio and genetic factors determine susceptibility to pediatric Crohn's disease | journal = Gastroenterology | volume = 146 | issue = 4 | pages = 929–31 | date = April 2014 | pmid = 24406470 | doi = 10.1053/j.gastro.2013.12.034 }} 11. ^{{cite journal | vauthors = Kikuta Y, Kusunose E, Sumimoto H, Mizukami Y, Takeshige K, Sakaki T, Yabusaki Y, Kusunose M | title = Purification and characterization of recombinant human neutrophil leukotriene B4 omega-hydroxylase (cytochrome P450 4F3) | journal = Archives of Biochemistry and Biophysics | volume = 355 | issue = 2 | pages = 201–5 | date = July 1998 | pmid = 9675028 | doi = 10.1006/abbi.1998.0724 }} 12. ^{{cite journal | vauthors = Hardwick JP | title = Cytochrome P450 omega hydroxylase (CYP4) function in fatty acid metabolism and metabolic diseases | journal = Biochemical Pharmacology | volume = 75 | issue = 12 | pages = 2263–75 | date = June 2008 | pmid = 18433732 | doi = 10.1016/j.bcp.2008.03.004 }} Further reading{{refbegin | 2}}
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