Pathways and products for the metabolism of vitamin D3 by cytochrome P450scc

被引:106
|
作者
Tuckey, Robert C. [1 ]
Li, Wei [2 ]
Zjawiony, Jordan K. [3 ,4 ]
Zmijewski, Michal A. [5 ,6 ]
Nguyen, Minh N. [1 ]
Sweatman, Trevor [7 ,8 ]
Miller, Duane [2 ]
Slominski, Andrzej [5 ,6 ]
机构
[1] Univ Western Australia, Sch Biomol Biomed & Chem Sci, M310, Crawley, WA 6009, Australia
[2] Univ Tennessee, Ctr Hlth Sci, Coll Pharm, Dept Pharmaceut Sci, Memphis, TN 38163 USA
[3] Univ Mississippi, Sch Pharm, Dept Pharmacognosy, Pharmaceut Sci Res Inst, University, MS 38677 USA
[4] Univ Mississippi, Sch Pharm, Natl Ctr Nat Prod Res, Pharmaceut Sci Res Inst, University, MS 38677 USA
[5] Univ Tennessee, Ctr Hlth Sci, Dept Pathol & Lab Med, Memphis, TN 38163 USA
[6] Univ Tennessee, Ctr Hlth Sci, Ctr Canc Res, Memphis, TN 38163 USA
[7] Univ Tennessee, Ctr Hlth Sci, Dept Pharmacol, Memphis, TN 38163 USA
[8] Univ Tennessee, Ctr Hlth Sci, Ctr Canc Res, Memphis, TN 38163 USA
关键词
CYP11A1; cytochrome p450scc; hydroxyvitamin D3; NMR; vitamin D3;
D O I
10.1111/j.1742-4658.2008.06406.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytochrome P450scc (CYP11A1) can hydroxylate vitamin D3 to produce 20-hydroxyvitamin D3 and other poorly characterized hydroxylated products. The present study aimed to identify all the products of vitamin D3 metabolism by P450scc, as well as the pathways leading to their formation. Besides 20-hydroxyvitamin D3, other major metabolites of vitamin D3 were a dihydroxyvitamin D3 and a trihydroxyvitamin D3 product. The dihydroxyvitamin D3 was clearly identified as 20,23-dihydroxyvitamin D3 by NMR, in contrast to previous reports that postulated hydroxyl groups in positions 20 and 22. NMR of the trihydroxy product identified it as 17 alpha,20,23-trihydroxyvitamin D3. This product could be directly produced by P450scc acting on 20,23-dihydroxyvitamin D3, confirming that hydroxyl groups are present at positions 20 and 23. Three minor products of D3 metabolism by P450scc were identified by MS and by examining their subsequent metabolism by P450scc. These products were 23-hydroxyvitamin D3, 17 alpha-hydroxyvitamin D3 and 17 alpha,20-dihydroxyvitamin D3 and arise from the three P450scc-catalysed hydroxylations occurring in a different order. We conclude that the major pathway of vitamin D3 metabolism by P450scc is: vitamin D3 -> 20-hydroxyvitamin D3 -> 20,23-dihydroxyvitamin D3 -> 17 alpha,20,23-trihydroxyvitamin D3. The major products dissociate from the P450scc active site and accumulate at a concentration well above the P450scc concentration. Our new identification of the major dihydroxyvitamin D3 product as 20,23-dihydroxyvitamin D3, rather than 20,22-dihydroxyvitamin D3, explains why there is no cleavage of the vitamin D3 side chain, unlike the metabolism of cholesterol by P450scc.
引用
收藏
页码:2585 / 2596
页数:12
相关论文
共 50 条
  • [1] The cytochrome P450scc system opens an alternate pathway of vitamin D3 metabolism
    Slominski, A
    Semak, I
    Zjawiony, J
    Wortsman, J
    Li, W
    Szczesniewski, A
    Tuckey, RC
    FEBS JOURNAL, 2005, 272 (16) : 4080 - 4090
  • [2] Kinetics of vitamin D3 metabolism by cytochrome P450scc (CYP11A1) in phospholipid vesicles and cyclodextrin
    Tuckey, Robert C.
    Nguyen, Minh N.
    Slominski, Andrzej
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2008, 40 (11): : 2619 - 2626
  • [3] 20-hydroxyvitamin D3, a product of vitamin D3 hydroxylation by cytochrome P450scc, stimulates keratinocyte differentiation
    Zbytek, Blazej
    Janjetovic, Zorica
    Tuckey, Robert C.
    Zmijewski, Michal A.
    Sweatman, Trevor W.
    Jones, Emily
    Nguyen, Minh N.
    Slominski, Andrzej T.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2008, 128 (09) : 2271 - 2280
  • [4] Metabolism of 1α-hydroxyvitamin D3 by cytochrome P450scc to biologically active 1α,20-dihydroxyvitamin D3
    Tuckey, Robert C.
    Janjetovic, Zorica
    Li, Wei
    Nguyen, Minh N.
    Zmijewski, Michal A.
    Zjawiony, Jordan
    Slominski, Andrzej
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2008, 112 (4-5): : 213 - 219
  • [5] Products of Vitamin D3 or 7-Dehydrocholesterol Metabolism by Cytochrome P450scc Show Anti-Leukemia Effects, Having Low or Absent Calcemic Activity
    Slominski, Andrzej T.
    Janjetovic, Zorica
    Fuller, Brian E.
    Zmijewski, Michal A.
    Tuckey, Robert C.
    Nguyen, Minh N.
    Sweatman, Trevor
    Li, Wei
    Zjawiony, Jordan
    Miller, Duane
    Chen, Tai C.
    Lozanski, Gerard
    Holick, Michael F.
    PLOS ONE, 2010, 5 (03):
  • [6] A pathway for the metabolism of vitamin D3:: Unique hydroxylated metabolites formed during catalysis with cytochrome P450scc (CYP11A1)
    Guryev, O
    Carvalho, RA
    Usanov, S
    Gilep, A
    Estabrook, RW
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (25) : 14754 - 14759
  • [7] Oriented nanostructures of cytochrome P450scc
    Guryev, OL
    Chernogolov, AA
    Usanov, SA
    FASEB JOURNAL, 1997, 11 (09): : A814 - A814
  • [8] In vivo evidence for a novel pathway of vitamin D3 metabolism initiated by P450scc and modified by CYP27B1
    Slominski, Andrzej T.
    Kim, Tae-Kang
    Shehabi, Haleem Z.
    Semak, Igor
    Tang, Edith K. Y.
    Nguyen, Minh N.
    Benson, Heather A. E.
    Korik, Elena
    Janjetovic, Zorica
    Chen, Jianjun
    Yates, Charles R.
    Postlethwaite, Arnold
    Li, Wei
    Tuckey, Robert C.
    FASEB JOURNAL, 2012, 26 (09): : 3901 - 3915
  • [9] REFINEMENT AND STRUCTURAL EVALUATION OF MODEL CYTOCHROME P450SCC 3D STRUCTURE
    VIJAYAKUMAR, S
    SALERNO, JC
    BIOPHYSICAL JOURNAL, 1993, 64 (02) : A48 - A48
  • [10] Cholesterol amperometric biosensor based on cytochrome P450scc
    Shumyantseva, V
    Deluca, G
    Bulko, T
    Carrara, S
    Nicolini, C
    Usanov, SA
    Archakov, A
    BIOSENSORS & BIOELECTRONICS, 2004, 19 (09): : 971 - 976