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Molecular Pharmacology

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Research ArticleArticle

Progesterone Receptor Membrane Component 1 Inhibits the Activity of Drug-Metabolizing Cytochromes P450 and Binds to Cytochrome P450 Reductase

Elzbieta Szczesna-Skorupa and Byron Kemper
Molecular Pharmacology March 2011, 79 (3) 340-350; DOI: https://doi.org/10.1124/mol.110.068478
Elzbieta Szczesna-Skorupa
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Byron Kemper
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Abstract

Progesterone receptor membrane component 1 (PGRMC1) has been shown to interact with several cytochromes P450 (P450s) and to activate enzymatic activity of P450s involved in sterol biosynthesis. We analyzed the interactions of PGRMC1 with the drug-metabolizing P450s, CYP2C2, CYP2C8, and CYP3A4, in transfected cells. Based on coimmunoprecipitation assays, PGRMC1 bound efficiently to all three P450s, and binding to the catalytic cytoplasmic domain of CYP2C2 was much more efficient than to a chimera containing only the N-terminal transmembrane domain. Down-regulation of PGRMC1 expression levels in human embryonic kidney 293 and HepG2 cell lines stably expressing PGRMC1-specific small interfering RNA had no effect on the endoplasmic reticulum localization and expression levels of P450s, whereas enzymatic activities of CYP2C2, CYP2C8, and CYP3A4 were slightly higher in PGRMC1-deficient cells. Cotransfection of cells with P450s and PGRMC1 resulted in PGRMC1 concentration-dependent inhibition of the P450 activities, and this inhibition was partially reversed by increased expression of the P450 reductase (CPR). In contrast, CYP51 activity was decreased by down-regulation of PGRMC1 and expression of PGRMC1 in the PGRMC1-deficient cells increased CYP51 activity. In cells cotransfected with CPR and PGRMC1, strong binding of CPR to PGRMC1 was observed; however, in the presence of CYP2C2, interaction of PGRMC1 with CPR was significantly reduced, suggesting that CYP2C2 competes with CPR for binding to PGRMC1. These data show that in contrast to sterol synthesizing P450, PGRMC1 is not required for the activities of several drug-metabolizing P450s, and its overexpression inhibits those P450 activities. Furthermore, PGRMC1 binds to CPR, which may influence P450 activity.

Footnotes

  • This work was supported by the National Institutes of Health National Institute of General Medical Sciences [Grant GM35897].

  • Article, publication date, and citation information can be found at http://molpharm.aspetjournals.org.

    doi:10.1124/mol.110.068478.

  • ABBREVIATIONS:

    P450s
    cytochromes P450
    CPR
    cytochrome P450 reductase
    PGRMC1
    progesterone receptor membrane component-1
    INSIG1
    insulin-induced gene 1
    GFP
    green fluorescent protein
    YFP
    yellow fluorescent protein
    ER
    endoplasmic reticulum
    siRNA
    small interfering RNA
    shRNA
    short hairpin RNA
    MSTFA
    N-methyl-N-trimethylsilyltrifluoroacetamine
    PCR
    polymerase chain reaction
    HEK
    human embryonic kidney
    DMEM
    Dulbecco's modified Eagle's medium
    GC/MS
    gas chromatography-mass spectrometry.

  • Received August 27, 2010.
  • Accepted November 16, 2010.
  • Copyright © 2011 The American Society for Pharmacology and Experimental Therapeutics
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Molecular Pharmacology: 79 (3)
Molecular Pharmacology
Vol. 79, Issue 3
1 Mar 2011
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Research ArticleArticle

Progesterone Receptor Membrane Component 1 Inhibits the Activity of Drug-Metabolizing Cytochromes P450 and Binds to Cytochrome P450 Reductase

Elzbieta Szczesna-Skorupa and Byron Kemper
Molecular Pharmacology March 1, 2011, 79 (3) 340-350; DOI: https://doi.org/10.1124/mol.110.068478

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Research ArticleArticle

Progesterone Receptor Membrane Component 1 Inhibits the Activity of Drug-Metabolizing Cytochromes P450 and Binds to Cytochrome P450 Reductase

Elzbieta Szczesna-Skorupa and Byron Kemper
Molecular Pharmacology March 1, 2011, 79 (3) 340-350; DOI: https://doi.org/10.1124/mol.110.068478
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