Ogle C K, Ogle J D, Keynton L, Nagy H, Alexander J W
Department of Surgery, Shriners Burns Institute, Cincinnati Medical Center, Ohio.
J Burn Care Rehabil. 1989 Mar-Apr;10(2):146-50. doi: 10.1097/00004630-198903000-00008.
The effect of in vivo administration of the immunomodulator TP-5 on the in vitro synthesis and release of C3, PGE2, and TXB2 by guinea pig alveolar, splenic, and peritoneal macrophages was studied. Three groups of animals were studied: unburned control, burned, and burned + TP-5. There was no significant difference in the production of C3, PGE2, or TXB2, by alveolar macrophages of the three groups of animals or by splenic macrophages of the three groups. There was a significant difference in the production of TXB2 by peritoneal macrophages between the unburned control compared with the burned and burned plus TP-5 groups. Our conclusion is that peritoneal macrophages seem to be controlled by mechanisms that are different from those that control alveolar or splenic macrophages.
研究了体内给予免疫调节剂TP - 5对豚鼠肺泡巨噬细胞、脾巨噬细胞和腹腔巨噬细胞体外合成和释放C3、前列腺素E2(PGE2)和血栓素B2(TXB2)的影响。研究了三组动物:未烧伤对照、烧伤和烧伤 + TP - 5组。三组动物的肺泡巨噬细胞或三组脾巨噬细胞产生C3、PGE2或TXB2的情况无显著差异。未烧伤对照组与烧伤组及烧伤加TP - 5组相比,腹腔巨噬细胞产生TXB2的情况存在显著差异。我们的结论是,腹腔巨噬细胞似乎受与控制肺泡或脾巨噬细胞不同的机制所调控。