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Research ArticleCARDIOVASCULAR

Urotensin-II-Converting Enzyme Activity of Furin and Trypsin in Human Cells in Vitro

Fraser D. Russell, Philip Kearns, Istvan Toth and Peter Molenaar
Journal of Pharmacology and Experimental Therapeutics July 2004, 310 (1) 209-214; DOI: https://doi.org/10.1124/jpet.104.065425
Fraser D. Russell
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Philip Kearns
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Istvan Toth
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Peter Molenaar
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Abstract

Human urotensin-II (hU-II) is processed from its prohormone (ProhU-II) at putative cleavage sites for furin and serine proteases such as trypsin. Although proteolysis is required for biological activity, the endogenous “urotensin-converting enzyme” (UCE) has not been investigated. The aim of this study was to investigate UCE activity in cultured human cells and in blood, comparing activity with that of furin and trypsin. In a cell-free system, hU-II was detected by high-performance liquid chromatography-mass spectrometry after coincubating 10 μM carboxyl terminal fragment (CTF)-ProhU-II with recombinant furin (2 U/ml, 3 h, 37°C) at pH 7.0 and pH 8.5, but not at pH 5.0, or when the incubating medium was depleted of Ca2+ ions and supplemented with 2 mM EDTA at pH 7.0. hU-II was readily detected in the superperfusate of permeabilized epicardial mesothelial cells incubated with CTF-ProhU-II (3 h, 37°C), but it was only weakly detected in the superperfusate of intact cells. Conversion of CTF-ProhU-II to hU-II was attenuated in permeabilized cells using conditions found to inhibit furin activity. In a cell-free system, trypsin (0.05 mg/ml) cleaved CTF-ProhU-II to hU-II, and this was inhibited with 35 μM aprotinin. hU-II was detected in blood samples incubated with CTF-ProhU-II (3 h, 37°C), and this was also inhibited with aprotinin. The findings revealed an intracellular UCE in human epicardial mesothelial cells with furin-like activity. Aprotinin-sensitive UCE activity was detected in blood, suggesting that an endogenous serine protease such as trypsin may also contribute to proteolysis of hU-II prohormone, if the prohormone is secreted into the circulation.

Footnotes

  • This study was supported by an National Health and Medical Research Council of Australia New Investigator grant (to F.D.R.).

  • DOI: 10.1124/jpet.104.065425.

  • ABBREVIATIONS: hU-II, human urotensin-II; pro-hU-II, urotensin-II prohormone; CTF-ProhU-II, 25-amino acid residue carboxyl terminal fragment of urotensin-II prohormone; DMEM, Dulbecco's modified Eagle's medium; HPLC, high-performance liquid chromatography; UCE, urotensin-converting enzyme; BNP, brain natriuretic peptide.

    • Received January 11, 2004.
    • Accepted March 8, 2004.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 310 (1)
Journal of Pharmacology and Experimental Therapeutics
Vol. 310, Issue 1
1 Jul 2004
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Research ArticleCARDIOVASCULAR

Urotensin-II-Converting Enzyme Activity of Furin and Trypsin in Human Cells in Vitro

Fraser D. Russell, Philip Kearns, Istvan Toth and Peter Molenaar
Journal of Pharmacology and Experimental Therapeutics July 1, 2004, 310 (1) 209-214; DOI: https://doi.org/10.1124/jpet.104.065425

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Research ArticleCARDIOVASCULAR

Urotensin-II-Converting Enzyme Activity of Furin and Trypsin in Human Cells in Vitro

Fraser D. Russell, Philip Kearns, Istvan Toth and Peter Molenaar
Journal of Pharmacology and Experimental Therapeutics July 1, 2004, 310 (1) 209-214; DOI: https://doi.org/10.1124/jpet.104.065425
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