Literature DB >> 20510674

Thromboxane A(2) increases endothelial permeability through upregulation of interleukin-8.

Su-Ryun Kim1, Soo-Kyung Bae, Hyun-Joo Park, Mi-Kyoung Kim, Koanhoi Kim, Shi-Young Park, Hye-Ock Jang, Il Yun, Yung-Jin Kim, Mi-Ae Yoo, Moon-Kyoung Bae.   

Abstract

Thromboxane A(2) (TXA(2)), a major prostanoid formed from prostaglandin H(2) by thromboxane synthase, is involved in the pathogenesis of a variety of vascular diseases. In this study, we report that TXA(2) mimetic U46619 significantly increases the endothelial permeability both in vitro and in vivo. U46619 enhanced the expression and secretion of interleukin-8 (IL-8), a major inducer of vascular permeability, in endothelial cells. Promoter analysis showed that the U46619-induced expression of IL-8 was mainly regulated by nuclear factor-kappaB (NF-kappaB). U46619 induced the activation of NF-kappaB through IkappaB kinase (IKK) activation, IkappaB phosphorylation and NF-kappaB nuclear translocation. Furthermore, the inhibition of IL-8 or blockade of the IL-8 receptor attenuated the U46619-induced endothelial cell permeability by modulating the cell-cell junctions. Overall, these results suggest that U46619 promotes vascular permeability through the production of IL-8 via NF-kappaB activation in endothelial cells. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20510674     DOI: 10.1016/j.bbrc.2010.05.106

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


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