Anoxia/reoxygenation-induced leukocyte-endothelial cell interactions

S Kokura, N Yoshida, T Yoshikawa - Free Radical Biology and Medicine, 2002 - Elsevier
S Kokura, N Yoshida, T Yoshikawa
Free Radical Biology and Medicine, 2002Elsevier
It is increasingly apparent that oxidants can play an important role in mediating specific cell
responses and expression of genes involved in degenerative pathophysiologic states, such
as inflammation. In particular, oxidant-induced activation of the multisubunit nuclear
transcription factor, NFκB, has been implicated in the transcriptional upregulation of
inflammatory genes like endothelial cell adhesion glycoproteins. A second emerging
concept is the recognition that the oxidant effects in cellular and molecular regulation may …
It is increasingly apparent that oxidants can play an important role in mediating specific cell responses and expression of genes involved in degenerative pathophysiologic states, such as inflammation. In particular, oxidant-induced activation of the multisubunit nuclear transcription factor, NFκB, has been implicated in the transcriptional upregulation of inflammatory genes like endothelial cell adhesion glycoproteins. A second emerging concept is the recognition that the oxidant effects in cellular and molecular regulation may be mediated by oxidant-induced loss of cellular oxidation-reduction (redox) balance. This review will provide an overview of our current understanding of leukocyte-endothelial cell interactions derived from in vitro studies of endothelial cell monolayers exposed to anoxia/reoxygenation, with specific emphasis on the molecular determinants mediating this inflammatory process and the contribution of reoxygenation-induced cellular redox imbalance to the activation of NFκB and the expression of endothelial surface adhesion molecules.
Elsevier