Beezhold D H, Lause D B
Department of Anatomy, Medical College of Georgia, Augusta 30912.
Immunol Invest. 1987 Aug;16(5):437-49. doi: 10.3109/08820138709087097.
Purified plasma fibronectin (Fn) enhanced the secretory activity of rat peritoneal exudate macrophages as measured by 35S-methionine incorporation into protein released into culture supernatants. Enhancement of protein secretion was dose-dependent and increased with time in culture. Addition of various concentrations of supernatant from cultures of macrophages with Fn resulted in a significant increase in thymocyte proliferation elicited by phytohaemagglutinin. The stimulatory activity of the supernatant was Fn dose-dependent and increased with increasing concentrations of macrophages. This thymocyte stimulatory effect was not due to the presence of Fn in the culture supernatant or to the minimal contamination with endotoxin detected in the Fn preparations. These data suggest that the inflammatory macrophage interaction with Fn results in the release of interleukin-1. They also are consistent with the reported ability of Fn to stimulate lymphocyte transformation.
纯化的血浆纤连蛋白(Fn)增强了大鼠腹腔渗出液巨噬细胞的分泌活性,这是通过将³⁵S-甲硫氨酸掺入释放到培养上清液中的蛋白质来测定的。蛋白质分泌的增强呈剂量依赖性,并随培养时间增加。添加来自用Fn培养的巨噬细胞培养物的各种浓度的上清液,导致植物血凝素引起的胸腺细胞增殖显著增加。上清液的刺激活性呈Fn剂量依赖性,并随着巨噬细胞浓度的增加而增加。这种胸腺细胞刺激作用不是由于培养上清液中存在Fn或Fn制剂中检测到的内毒素的微量污染。这些数据表明,炎症巨噬细胞与Fn的相互作用导致白细胞介素-1的释放。它们也与报道的Fn刺激淋巴细胞转化的能力一致。