Platelet-activating factor increases endothelial [Ca2+]iand NO production in individually perfused intact microvessels
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Open Access
- 1 June 2005
- journal article
- Published by American Physiological Society in American Journal of Physiology-Heart and Circulatory Physiology
- Vol. 288 (6) , H2869-H2877
Abstract
We have demonstrated that inhibition of NO synthase (NOS) in endothelial cells by either the NOS inhibitor Nω-monomethyl-l-arginine (l-NMMA) or the internalization of caveolin-1 scaffolding domain attenuated platelet-activating factor (PAF)-induced increases in microvessel permeability ( Am J Physiol Heart Circ Physiol 286: H195–H201, 2004) indicating the involvement of an NO-dependent signaling pathway. To investigate whether an increase in endothelial cytoplasmic Ca2+concentration ([Ca2+]i) is the initiating event and Ca2+-dependent NO production is crucial for permeability increases, PAF (10 nM)-induced changes in endothelial [Ca2+]iand NO production were measured in individually perfused rat mesenteric venular microvessels via fluorescence microscopy. When venular microvessels were exposed to PAF, endothelial [Ca2+]iincreased from 69 ± 8 nM to a peak value of 374 ± 26 nM within 3 min and then declined to a sustained level at 190 ± 12 nM after 15 min. Inhibition of NOS did not modify PAF-induced increases in endothelial [Ca2+]i. PAF-induced NO production was visualized and quantified at cellular levels in individually perfused microvessels using 4,5-diaminofluorescein diacetate and fluorescence imaging. Increased fluorescence intensity (FI), which is an indication of increased NO production, occurred in 75 ± 7% of endothelial cells in each vessel. The mean maximum FI increase was 140 ± 7% of baseline value. This increased FI was abolished by pretreatment of the vessel with l-NMMA and attenuated in the absence of extracellular Ca2+. These results provide direct evidence from intact microvessels that increased endothelial [Ca2+]iis the initial signal that activates endothelial NOS, and the subsequent increased NO production contributes to PAF-induced increases in microvessel permeability.Keywords
This publication has 37 references indexed in Scilit:
- Internalization of caveolin-1 scaffolding domain facilitated by Antennapedia homeodomain attenuates PAF-induced increase in microvessel permeabilityAmerican Journal of Physiology-Heart and Circulatory Physiology, 2004
- Table of Contents—A new look for the New YearAmerican Journal of Physiology-Cell Physiology, 2003
- Mechanisms of Heterogeneous Endothelial Cytoplasmic Calcium Increases in Venular MicrovesselsMicrocirculation, 2002
- Insulin-stimulated Activation of eNOS Is Independent of Ca2+ but Requires Phosphorylation by Akt at Ser1179Journal of Biological Chemistry, 2001
- Ca2+ signalling and PKCα activate increased endothelial permeability by disassembly of VE—cadherin junctionsThe Journal of Physiology, 2001
- Stimulation of NO Production and of eNOS Phosphorylation in the Microcirculation in VivoMicrovascular Research, 2000
- 17β-Estradiol Regulation of Human Endothelial Cell Basal Nitric Oxide Release, Independent of Cytosolic Ca 2+ MobilizationCirculation Research, 1997
- Platelet Activating Factor Modulates Microvascular Permeability through Nitric Oxide SynthesisMicrovascular Research, 1995
- Simultaneous Measurements of Ca2+and Nitric Oxide in Bradykinin-Stimulated Vascular Endothelial CellsCirculation Research, 1995
- Role of nitric oxide in modulating permeability of hamster cheek pouch in response to adenosine 5?-diphosphate and bradykininInflammation, 1992