Vassalli J D, Hamilton J, Reich E
Cell. 1976 Jun;8(2):271-81. doi: 10.1016/0092-8674(76)90011-8.
Plasminogen activator production by cultured mouse peritoneal macrophages can be modulated in vitro by low concentrations of various pharmacologically active molecules. Glucocorticoid hormones and their synthetic derivatives, as well as cholera toxin, colchicine, and vinblastine markedly inhibit production of this enzyme without affecting other important macrophage functions. The effect of glucocorticoids is of particular interest, both because their relative in vivo anti-inflammatory potencies correlate exactly with their effect on plasminogen activator production in culture and because this effect occurs at near physiological concentrations. In view of the correlations established in other systems between plasminogen activator production and cell migration, we have also examined the age of the macrophages in thioglycollate-induced exudates. Confirming the results of Van Furth and Cohn (1968), we have found that the majority of these cells are young, having recently replicated and arrived in the peritoneal cavity. Using a fibrinagar overlay technique which allowed us to determine the production of plasminogen activator by individual cells. we have found that the majority of these cells produce the enzyme. The potential roles of plasminogen activator in monocyte migration and the relationship of this enzyme to the anti-inflammatory effect of gluccorticoids are correlated and emphasized.
培养的小鼠腹腔巨噬细胞产生纤溶酶原激活物的过程,在体外可受到低浓度各种药理活性分子的调节。糖皮质激素及其合成衍生物,以及霍乱毒素、秋水仙碱和长春花碱,均可显著抑制这种酶的产生,而不影响巨噬细胞的其他重要功能。糖皮质激素的作用尤其令人关注,这既是因为它们在体内的相对抗炎效力与它们对培养物中纤溶酶原激活物产生的影响完全相关,也是因为这种影响发生在接近生理浓度时。鉴于在其他系统中已确立的纤溶酶原激活物产生与细胞迁移之间的相关性,我们还研究了巯基乙酸诱导渗出液中巨噬细胞的年龄。证实了范·弗思和科恩(1968年)的结果,我们发现这些细胞中的大多数是年轻的,它们最近进行了复制并进入了腹腔。使用一种纤维蛋白琼脂覆盖技术,使我们能够确定单个细胞产生纤溶酶原激活物的情况。我们发现这些细胞中的大多数都产生这种酶。纤溶酶原激活物在单核细胞迁移中的潜在作用以及这种酶与糖皮质激素抗炎作用的关系得到了关联和强调。