Abscess formation is a classic host response to infection by many pathogenic microorganisms. Here, we studied the role of prostaglandins (PGs) and their signal transduction in abscess formation. Zymosan was injected into the pleural cavity of rats. Expression of enzymes involved in PG synthesis, their receptors, and cytokines in exudate leukocytes and abscesses were analyzed by polymerase chain reaction, Western blotting, and immunohistochemistry. Treatment with ketorolac, a cyclooxygenase (COX)-1 inhibitor, or N- [2-cyclohexyloxy-4-nitrophenyl] methanesulfonamide (NS-398), a COX-2 inhibitor, reduced the size of abscesses and the number of cells recovered from the abscess. COX-2 was detected in leukocytes of the exudate and a marginal area of abscesses. Among detected terminal PG synthases, the major one was cytosolic PGE synthase. Membrane-bound PGE synthase (mPGES)-1 was detected in cells that were similar to the COX-2-expressing cells in morphology and localization. A high level of the E-prostanoid (EP) 2 receptor and a low level of the EP 4 receptor were detected. The expression pattern of the EP 2 receptor paralleled that of COX-2 and mPGES-1. 11,15-O-Dimethyl PGE 2 (ONO-AE1-259), an EP 2 receptor agonist, and rolipram, a phosphodiesterase type-4 inhibitor, reversed the effects of COX inhibitors on abscess formation. In contrast, 16-(3-methoxymethyl) phenyl--tetranor-3,7-dithia PGE 1 (ONO-AE1-329), an EP 4 receptor agonist, did not reverse the effects of NS-398. Moreover, NS-398 reduced the mRNA levels in exudate leukocytes of some proinflammatory and fibrogenic cytokines, which was reversed by ONO-AE1-259. These results suggest that PGE 2 generated via COX-1 and COX-2 may interact with the EP 2 receptor and may up-regulate in cAMP-dependent fashion the production of cytokines that promote abscess formation.Abscess formation is a complex host response that involves fibrin deposition and recruitment of leukocytes as well as other processes that have not been completely elucidated. It has been viewed as a host defense strategy: a fibrous capsule localizes invading microorganisms and presumably protects the host from disseminated infection. However, microorganisms sequestered within a fibrin capsule are protected from normal host clearance mechanisms, thereby permitting unopposed proliferation of the microorganisms (Brook, 2002). Thus, an abscess is difficult to treat with antimicrobial therapy and usually requires surgical intervention.Prostanoids, including prostaglandin (PG) and thromboxane (TX), are lipid mediators that regulate numerous processes in the body, including modulation of immune and inflammatory responses. Prostanoids are produced when arachidonic acid is released from the plasma membrane by phospholipase A 2 and metabolized by cyclooxygenases (COXs) and specific terminal PG synthases. Prostanoid production depends on the activity of two COX isoforms, COX-1 and COX-2. COX-1 is present in most cells and its expression is constitutive. In contrast, COX-2 expression is low or undetectabl...