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Cloning, sequencing, and cDNA-directed expression of the rat renal CYP4A2: Arachidonic acid ω-hydroxylation and 11,12-epoxidation by CYP4A2 protein

  • Mong Heng Wang
    ,
  • David E. Stec
    ,
  • Michael Balazy
    ,
  • Vladimir Mastyugin
    ,
  • Chung S. Yang
    ,
  • Richard J. Roman
  • New York Medical College
    ,
  • Medical College of Wisconsin
    ,
  • Rutgers - The State University of New Jersey, New Brunswick
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

20-Hydroxy-5,8,11,14-eicosatetraenoic acid (20-HETE), the ω- hydroxylation product of arachidonic acid, is the major metabolite produced in the kidney. It has potent biological effects on renal tubular and vascular functions and on the long-term control of arterial pressure. The synthesis of 20-HETE is catalyzed by enzymes of the CYP4A family, among which CYP4A2 is the most abundant isozyme expressed in the kidneys of rats. We have cloned and sequenced the CYP4A2 cDNA from the kidney of Lewis-Wistar rats and directed its expression using baculovirus and Sf9 insect cells. A high level of expression of CYP4A2 was evident by Northern, Western, and spectral analyses revealing a P450 content of 0.3 nmol/mg microsomal protein. To study CYP4A2-catalyzed arachidonic acid ω-hydroxylation, SP9 cells were coinfected with CYP4A2 and NADPH cytochrome P450 oxidoreductase (OR) recombinant viruses. CYP4A2/OR membranes metabolized lauric acid at a high rate (7 and 5.5 nmol/min/nmol P450 in the presence and absence of b5, respectively). However, arachidonic acid ω-hydroxylase activity was barely detectable. When purified OR was added to the membranes expressing CYP4A2 protein, a concentration-dependent production of 20-HETE was observed. Maximal synthesis of 20-HETE of 0.89 nmol/min/nmol P450 was achieved at OR:CYP4A2 ratio of 14:1. The ω-hydroxylation of arachidonic acid was dependent on the presence of b5. Furthermore, increasing OR concentrations yielded additional arachidonic acid metabolite identified by GC/MS as 11,12-EET. Microsomes prepared from isolated renal microvessels selectively expressed CYP4A2 protein and readily metabolized arachidonic acid to two major metabolites, 20-HETE and 11,12-DHET, the hydrolytic metabolite of 11,12-EET. It is suggested that CYP4A2 functions as the renal microvessel arachidonate ω- hydroxylase and that it can also catalyze the 11,12-epoxidation of arachidonic acid.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 240-250 (11 pages)

Journal (Volume, Issue Number)

Archives of Biochemistry and Biophysics (Volume 336, Issue 2)

Publication milestones

  • Published - 12/15/1996

Publication status

Published - 12/15/1996

ISSN

0003-9861

Publication IDs

  • Scopus: 0030589540
  • PubMed: 8954571

Publication metrics

Metrics

SciVal
FWCI
2.34
SciVal
Author count
7
SciVal
citations
71
SciVal
Paper percentile
92
SciVal
Top percentile
10
Scopus
citations
Fractional count
1
Fractional count
0.14
Fractional count
6
Fractional count
0.86
Fractional count
1
Fractional count
1

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Captures
14
Citation count
71

Funding Details

1Supported in part by grants from the National Institutes of Health, HL34300 and HL36279. 2 To whom correspondence should be addressed. Fax: (914) 993-4303.