Synergy of interleukin 1 (IL-1) with arachidonic acid and A23187 in stimulating PGE synthesis in human fibroblasts: IL-1 stimulates fibroblast cyclooxygenase
Autor: | Gerald J. Roth, Joseph H. Korn, Shih-Yieh Ho, Elaine Downie |
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Rok vydání: | 1989 |
Předmět: |
medicine.medical_treatment
Immunology Stimulation Arachidonic Acids Pharmacology Dinoprostone Pathology and Forensic Medicine Dermal fibroblast chemistry.chemical_compound medicine Humans Immunology and Allergy Fibroblast Calcimycin Arachidonic Acid biology Cell Membrane Interleukin Drug Synergism Biological activity Fibroblasts medicine.anatomical_structure Biochemistry chemistry Prostaglandin-Endoperoxide Synthases biology.protein Arachidonic acid Cyclooxygenase Interleukin-1 Prostaglandin E |
Zdroj: | Clinical Immunology and Immunopathology. 50:196-204 |
ISSN: | 0090-1229 |
DOI: | 10.1016/0090-1229(89)90128-1 |
Popis: | The stimulation of prostaglandin E (PGE) synthesis by interleukin 1 (IL-1) has important physiologic effects in many target tissues. The mechanisms(s) whereby IL-1 stimulates PGE synthesis is not well understood. Two alternative mechanisms have been postulated: hydrolysis of membrane phospholipid with release of arachidonic acid substrate and induction of cyclooxygenase activity. We examined these mechanisms in IL-1 stimulation of human dermal fibroblast PGE synthesis. IL-1 failed to induce release of previously incorporated radiolabeled arachidonic acid from fibroblasts under conditions where there was a 30-fold or greater stimulation of PGE synthesis. The calcium ionophore, A23187, gave much less stimulation of PGE synthesis while inducing 30–100% release of incorporated [14C]arachidonic acid. There was marked synergy between IL-1 and agents which increased availability of arachidonic acid. For example, the combination of IL-1 and A23187, used at concentrations where neither agent alone stimulated PGE synthesis, increased PGE synthesis from 3.1 to 22.5 ng/ml; similar synergy was seen between IL-1 and exogenous arachidonic acid. To examine a possible effect of IL-1 on cyclooxygenase synthesis, fibroblast cyclooxygenase was measured by radioimmunoassay. Following treatment with IL-1, fibroblasts demonstrated a two- to threefold increase in content of immunoreactive cyclooxygenase. These results suggest that IL-1 increases fibroblast PGE synthesis by a mechanism(s) other than making available increased membrane arachidonic acid, and that at least part of its effect may be mediated by induction of cyclooxygenase. Furthermore, the effect of IL-1 on fibroblast PGE synthesis is markedly potentiated by agents which increase available substrate. |
Databáze: | OpenAIRE |
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