Thromboxane synthesis is increased by upregulation of cytosolic phospholipase A2 and cyclooxygenase-2 in peripheral polymorphonuclear leukocytes during bacterial infection in childhood

Am J Hematol. 2003 Feb;72(2):115-20. doi: 10.1002/ajh.10280.

Abstract

Prostaglandins (PGs) and thromboxane (TX) are important mediators of inflammation. Recent studies revealed that PG and TX synthesis is controlled by the regulation of PG- and TX-synthesizing enzymes. In this study, we examined the TX synthesis and the expression of TX-synthesizing enzymes in activated peripheral polymorphonuclear leukocytes (PMNs) obtained from children with bacterial infection. Blood samples were obtained from controls and patients with bacterial infection. A23187-stimulated production of TXB(2), a stable metabolite of TXA(2) in PMNs, was measured by a specific radioimmunoassay. The mRNA expression of cytosolic phospholipase A(2) (cPLA(2)), cyclooxygenase (COX)-1, COX-2, and TXA(2) synthase was determined by RT-PCR. The synthesis of TXB(2) in PMNs was significantly increased in the patients [925.0 (550.0-1100.0) pg/10(6) cells], compared with the controls [550.0 (450.0-775.0) pg/10(6) cells]. The mRNA expression for cPLA(2) and COX-2 in PMNs was also enhanced in the patients. The results indicate that TX production in PMNs is significantly increased through possible transcriptional mechanisms of cPLA(2) and COX-2 during bacterial infection in children. The upregulation of TXA(2) synthesis may contribute to the process of acute inflammatory reaction caused by bacterial infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Anti-Bacterial Agents / pharmacology
  • Bacterial Infections / immunology
  • Bacterial Infections / metabolism*
  • Calcimycin / pharmacology
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Cytosol / enzymology
  • Female
  • Humans
  • Infant
  • Inflammation / metabolism
  • Inflammation / pathology
  • Isoenzymes / genetics*
  • Male
  • Membrane Proteins
  • Neutrophils / drug effects
  • Neutrophils / enzymology
  • Neutrophils / metabolism*
  • Phospholipases A / genetics*
  • Phospholipases A2
  • Prostaglandin-Endoperoxide Synthases / genetics*
  • RNA, Messenger / analysis
  • Thromboxane A2 / genetics
  • Thromboxane B2 / biosynthesis*
  • Up-Regulation

Substances

  • Anti-Bacterial Agents
  • Isoenzymes
  • Membrane Proteins
  • RNA, Messenger
  • Calcimycin
  • Thromboxane B2
  • Thromboxane A2
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • PTGS1 protein, human
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Phospholipases A
  • Phospholipases A2