Nitric oxide production from a macrophage cell line: Interaction with autologous and allogeneic lymphocytes

✍ Scribed by Ken-Ichi Isobe; Izumi Nakashima

• Publisher: John Wiley and Sons
• Year: 1993
• Tongue: English
• Weight: 593 KB
• Volume: 53
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.240530304

✦ Synopsis

The indirect stimulation of macrophages to produce nitrite was examined by using the macrophage cell line J774. J774 spontaneously produced nitrite, when cultured at high concentration. J774 cultured in low concentration ( < 1 O4 cells in 100 p,I) barely produced nitrite. J774 cultured in low concentration produced a large amount of nitrite by the co-culture of nonadherent spleen cells or nonadherent peritoneal exudate cells, which were stimulated with con A, anti-CD3, or staphylococcal enterotoxin A. 1774 (BALB/c derived: H-2d) cultured with either syngeneic (BALBlc I or allogeneic (B6; H-2b 61 OBR; H-2k) nonadherent lymphocytes, which were stimulated with conA or anti-CD3, produced nitric oxide. However, 1774 produced nitric oxide by stimulation with SEA only when co-cultured with SEA-reactkc. T lymphocytes. Peritoneal exudate cells from mice, which did not proliferate by the stimulation of conA or anti-CD3, proliferated well by the addition of L-arginine homologue, NC-monomethyl-L-arginine. The proliferation of nonadherent peritoneal exudate cells stimulated with conA or anti-CD3 was suppressed by the addition of peritoneal macrophages. This suppression was abolished by the addition of NG-monomethyl-L-arginine.