O’Brien et al found that ET inhibited PMN phagocytosis of opsonized B. anthracis [21]. Pretreatment of PMNs with ET profoundly reduced superoxide production in response to either LPS or muramyl dipeptide. Crawford et al demonstrated that ET impaired PMN NADPH oxidase activation and selleck compound downstream N-formyl-methionine-leucine-phenylalanine (fMLP)-induced superoxide production

[37]. Taken together, these studies indicate that ET down-regulates PMN phagocytic and oxidative functions. Other studies have focused on the impact of ET on PMN chemotaxis and migration [9, 22]. In the current studies, ET did not alter the PMN chemotactic response to IL-8 in an EC-free system (Figure 2A). To address concerns that calcein is a Ca2+-binder and would interfere with any Ca2+-mediated ET AZD1480 manufacturer effect, these experiments were performed in the absence of the fluoroprobe. Even in the absence of calcein, ET had no effect on IL-8 chemotaxis of PMNs (Figure 2B). Chemotaxis was not as vigorous in the latter experiment, and this may be secondary to differences in methodology; mainly the use of a modified Boyden chambers, a shorter incubation time, as well as a different means of measuring PMN migration. Wade et al found that ET stimulated directed neutrophil migration without having any effect on unstimulated random migration [22]. They also found that although ET increased cAMP in PMNs, the absolute

level of that increase was < 1% of that caused by the Bordetella pertussis toxin. In contrast, Szarowicz et al found that ET reduces chemoattractant-stimulated PMN actin assembly, chemokinesis, chemotaxis and polarization [9]. In PMNs, ET provoked

a > 50-fold increase in cAMP and a 4-fold increase in PKA phosphorylation. The differences between our findings and these other reports may be attributed to oxyclozanide dissimilar techniques. For instance, Wade et al measured chemotaxis of PMNs preincubated for 1 h with ET in an agarose-gel based system, both of which were EC-free [22], whereas Szarowicz’s group utilized video microscopy to study adherence of PMNs preincubated for 2 h with ET to a fibronectin-coated surface [9]. To our knowledge, none of these previous reports studied PMN migration in the context of the endothelial paracellular pathway. Another potential explanation for these disparities may be due to differences in potency of various EF preparations and their abilities to generate cAMP. Of note, the EF preparation offered by List Biologics is the least potent (personal communication, Dr. Erik Hewlett, University of Virginia, Charlottesville). Far less is known about the Citarinostat direct effect of ET on ECs. Hong et al demonstrated that ET reorganizes the cytoskeleton and inhibits chemotaxis of human microvascular ECs [7]. Tessier’s group found that ET induces a gradual increase in transendothelial electrical resistance (TEER) across human umbilical vein EC monolayers cultured on collagen-coated inserts.