Nitric Oxide Synthesis in Murine Peritoneal Macrophages by Antithrombin III.
- Author:
Jae Yong KWAK
1
;
Sang Youel PARK
;
Hae Su LEE
;
Myung Hee SOHN
;
Chang Yeol YIM
Author Information
1. Department of Internal Medicine, Chonbuk National University Medical School.
- Publication Type:Original Article
- Keywords:
Antithrombin III;
Nitric oxide;
Macrophage;
Heparin
- MeSH:
Animals;
Antibodies;
Antithrombin III*;
Arginine;
Cytokines;
Hemostasis;
Heparin;
Immunoglobulin G;
Indicators and Reagents;
Interferon-gamma;
Interleukin-1;
Macrophage Activation;
Macrophages;
Macrophages, Peritoneal*;
Mice;
Nitric Oxide Synthase Type II;
Nitric Oxide*;
omega-N-Methylarginine;
Polymyxin B;
Tumor Necrosis Factor-alpha
- From:Korean Journal of Hematology
1997;32(2):234-247
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: During the development of inflammatory responses, various cytokines including interferon-gamma (IFN-gamma), tumor necrosis factor-alpha (TNF), interleukin-1 (IL-1) which activate macrophages to synthesize nitric oxide (NO) and hemostatic cascades are secreted. However, effects of various factors involved in hemostasis on NO synthesis have been little known. In this report, we studied the effects of antithrombin III (AT-III) on NO synthesis by thioglycollate-elicited peritoneal macrophages of BALB/c mouse. METHODS: Macrophages were obtained from BALB/c mice injected with 3% thioglycollate and cultured with or without various reagents. Nitrite concentration was measured using a modification of Griess reaction. Immunoblot analysis for inducible nitric oxide synthase (iNOS), AT-III receptor binding study and assay of TNF secretion were performed. RESULTS: AT-III alone did not induce nitrite synthesis by macrophages. However, AT-III induced nitrite synthesis in the presence of IFN-gamma in a dose dependant manner. iNOS was also expressed in macrophages by the treatment with IFN-gamma/AT-III. Addition of 0.5mM NG-monomethyl-L-arginine markedly inhibited IFN-gamma/AT-III-induced nirtite synthesis. Treatment with 5microgram/mL polymyxin B, which inactivates LPS, did not inhibit IFN-gamma/AT- III-induced nitrite synthesis, excluding inadvertent endotoxin contamination. Addition of rabbit anti-human AT-III polyclonal IgG antibodies, but not control rabbit IgG, inhibited IFN-gamma/ AT-III-induced nitrite production. Treatment of macrophages with heparin did not augment, but inhibited both IFN-gamma/AT-III- and IFN-gamma/LPS-induced nitrite synthesis. CONCLUSION: Our results indicated that AT-III acted as a modulator of macrophage activation for L-arginine dependent NO synthesis and that AT-III might be an important molecule in the regulation of immune responses by macrophage activation to induce NO synthesis as well as in the regulation of hemostasis. Heparin was not a cofactor in the AT-III-induced NO synthesis.
