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Nitric oxide and endothelin secretion by brain microvessel endothelial cells: Regulation by cyclic nucleotides
Author(s) -
DurieuTrautmann O.,
Fédérici C.,
Crémi C.,
FoignantChaverot N.,
Roux F.,
Claire M.,
Strosberg A. D.,
Couraud P. O.
Publication year - 1993
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041550114
Subject(s) - microvessel , endothelial stem cell , biology , secretion , endothelin 1 , microbiology and biotechnology , second messenger system , nitric oxide , endothelins , calmodulin , endothelin receptor , medicine , endocrinology , in vitro , signal transduction , biochemistry , receptor , angiogenesis , cancer research , enzyme
Endothelin (ET)‐1 was originally characterized as a potent vasoconstrictor peptide secreted by vascular endothelial cells. It possesses a wide range of biological activities within the cardiovascular system and in other organs, including the brain. Also secreted by endothelial cells, nitric oxide (NO), has recently been identified as a relaxing factor, as well as a pleiotropic mediator, second messenger, immune defence molecule, and neurotransmitter. Most of the data concerning the secretion of these two agents in vitro has been collected from studies on macrovascular endothelial cells. Given the remarkable heterogeneity of endothelia in terms of morphology and function, we have analyzed the ability of brain microvessel endothelial cells in vitro to release ET‐1 and NO, which, at the level of the blood‐brain barrier, have perivascular astrocytes as potential targets. The present study was performed with immortalized rat brain microvessel endothelial cells, which display in culture a non transformed phenotype. Our data demonstrate that: (1) these cells release NO when induced by IFNγ and TNFα, (2) they constitutively secrete ET‐1, and (3) cAMP potentiates the cytokine‐induced NO release and exerts a biphasic regulation on ET‐1 secretion: micromolar concentrations of 8‐Br‐cAMP inhibit and higher doses stimulate ET‐1 secretion. This stimulation is blocked by EGTA and the calmodulin antagonist W7, but not by protein kinase C inhibitors, suggesting the involvement of the calmodulin branch of the calcium messenger system. These results suggest that cerebral microvessel endothelial cells may participate in vivo to the regulation of glial activity in the brain through the release of NO and ET‐1. © 1993 Wiley‐Liss, Inc.