Acute tissue-type plasminogen activator release in human microvascular endothelial cells: The roles of Gαq, PLC-β, IP3 and 5,6-epoxyeicosatrienoic acid

James A. S. Muldowney III; Corrie A. Painter; Elaine Sanders-Bush; Nancy J. Brown; Douglas E. Vaughan

doi:10.1160/TH05-02-0092

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2007; 97(02): 263-271
DOI: 10.1160/TH05-02-0092

Endothelium and Vascular Development

Schattauer GmbH

Acute tissue-type plasminogen activator release in human microvascular endothelial cells: The roles of Gα_q, PLC-β, IP₃ and 5,6-epoxyeicosatrienoic acid

James A. S. Muldowney III

¹Department of Medicine, Division of Cardiovascular Medicine and Department of Medicine

,

Corrie A. Painter

¹Department of Medicine, Division of Cardiovascular Medicine and Department of Medicine

,

Elaine Sanders-Bush

³Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee, USA

,

Nancy J. Brown

²Division of Clinical Pharmacology

,

Douglas E. Vaughan

¹Department of Medicine, Division of Cardiovascular Medicine and Department of Medicine

³Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee, USA

› Author Affiliations

Abstract

Summary

The acute physiologic release of tissue-type plasminogen activator (t-PA) from the endothelium is critical for vascular homeostasis. This process is prostacyclin- and nitric oxide (NO)-independent in humans. It has been suggested that calcium signaling and endothelial-derived hyperpolarizing factors (EDHF) may play a role in t-PA release. G-protein-coupled receptor-dependent calcium signaling is typically Gα_q -dependent. EDHFs have been functionally defined and in various tissues are believed to be various regioisomers of the epoxyeicosatrienoic acids (EETs). We tested the hypothesis in vitrothat thrombin-stimulated t-PA release from human microvascular endothelial cells (HMECs) is both Gα_q - and EDHF-dependent. Conditioned media was harvested following thrombin stimulation, and t-PA antigen was measured by ELISA. Thrombin-induced t-PA release was limited by a membrane-permeable Gα_q inhibitory peptide, the PLC-β antagonist U73122, and the IP3 receptor antagonist 2-aminoethoxyphenylborane, while the Gα_q agonist Pasteurellatoxin modestly induced t-PA release. The cytochrome P450 (CYP450) inhibitor, miconazole, and the arachidonic acid epoxygenase inhibitor MS-PPOH inhibited thrombin-stimulated t-PA release, while 5,6-EET-methyl ester stimulated t-PA release. The 5,6- and 14,15-EET antagonist, 14,15-epoxyeicosa-5(Z)- enoic acid, inhibited t-PA release at the 100 µM concentration. However, thrombin-stimulated t-PA release was unaffected by the prostacyclin and NO inhibitors ASA and L-NAME, as well as the potassium channel inhibitors TEA, apamin and charybdotoxin. These studies suggest that thrombin-stimulated t-PA release is Gα_q-, PLC-β -, IP₃ -, and 5,6-EET-dependent while being prostacyclin-, NO- and K + channel-independent in HMECs.

Keywords

Tissue-type plasminogen activator - signal transduction - pharmacology - thrombin - protease-activated receptor - epoxyeicosatrienoic acids (EET’s)

Full Text

References

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