Hypoxia modulates lipopolysaccharide induced TNF-α expression in murine macrophages

Abstract

The pro-inflammatory activity of Tumor necrosis factor-alpha (TNF-α) together with tissue hypoxia determine the clinical outcome in sepsis and septic shock. p38 MAPKinase is the primary intracellular signaling pathway that regulates lipopolysaccharide (LPS)-induced TNF-α biosynthesis, however, the effect of hypoxia on LPS mediated activation of p38 is not known. Here we report that SB203580, a specific p38 MAPK inhibitor, which completely abolished LPS-induced TNF-α expression by the mouse macrophage cell RAW264.7 in normoxic conditions, lost the inhibitory effect in hypoxic conditions. Hypoxia did not modulate expression of p38 MAPK, but increased that of p-MK2, a downstream target of p38 MAPK. In LPS induced endotoxemia mice model SB203580 had no inhibitory effect on the serum levels of TNF-α. Furthermore, hypoxia inducible factor-1alpha (HIF-1α) was detected in vivo after LPS administration but its expression was not affected by SB203580. Our data indicate that LPS induced p38 MAPK activation was enhanced by hypoxia and consequently increased TNF-α secretion. Furthermore, the induction of HIF-1α in mice with endotoxemia suggested a synergistic effect on p38 mediated TNF-α expression. These findings provide new insights on the pathophysiological effects of hypoxia in sepsis and septic shock.