Chiou W J, Bonin P D, Singh J P
Department of Cardiovascular Pharmacology, Lilly Research Laboratories, Indianapolis, IN 46285.
J Immunol. 1990 Oct 1;145(7):2155-60.
Our studies show that in connective tissue cells, induction of PGE2 synthesis in response to IL-1 requires costimulation with platelet-derived growth factor (PDGF) or fibroblast growth factor (FGF). In cells incubated in medium containing fresh serum, IL-1 induced a dose-dependent synthesis of PGE2. However, when the cells were incubated in medium containing low serum or platelet poor plasma (lacking PDGF), IL-1 alone failed to induce PGE2 synthesis. PGE2 synthesis was restored when platelet poor plasma was supplemented with PDGF. Addition of PDGF or FGF together with IL-1 resulted in a 14- and 66-fold stimulation of PGE2 synthesis, respectively. Stimulation was dependent on the concentration of both IL-1 and the growth factor. PGE2 synthesis was also dependent on the synthesis of new proteins. In cells simultaneously treated with IL-1 and PDGF, PGE2 synthesis was initiated after a lag of 2 to 3 h, proceeded first with a rapid rate for 6 h, and then with a slower rate through 24 h. PGE2 synthesis during the latter, slower phase was greatly enhanced by pretreatment with PDGF, but not by pretreatment with IL-1. PDGF pretreatment also resulted in maintenance of 10- to 12-fold higher cell surface IL-1-binding during this phase. These data provide evidence for potentially novel interactions between PDGF and IL-1 activities, one of which is the modulation of IL-1 receptors by PDGF. Furthermore, these studies suggest that by virtue of their effect on IL-1 activities, PDGF and FGF may play additional roles in connective tissues, including an indirect role in inflammatory processes.
我们的研究表明,在结缔组织细胞中,白细胞介素-1(IL-1)诱导前列腺素E2(PGE2)合成需要与血小板衍生生长因子(PDGF)或成纤维细胞生长因子(FGF)共同刺激。在含有新鲜血清的培养基中孵育的细胞中,IL-1诱导了PGE2的剂量依赖性合成。然而,当细胞在含有低血清或血小板贫乏血浆(缺乏PDGF)的培养基中孵育时,单独的IL-1未能诱导PGE2合成。当血小板贫乏血浆补充PDGF时,PGE2合成得以恢复。PDGF或FGF与IL-1一起添加分别导致PGE2合成增加14倍和66倍。刺激取决于IL-1和生长因子的浓度。PGE2合成也依赖于新蛋白质的合成。在用IL-1和PDGF同时处理的细胞中,PGE2合成在延迟2至3小时后开始,首先以快速速率进行6小时,然后以较慢速率持续24小时。在后一较慢阶段的PGE2合成通过PDGF预处理得到极大增强,但IL-1预处理则不然。PDGF预处理在此阶段还导致细胞表面IL-1结合维持在高10至12倍的水平。这些数据为PDGF和IL-1活性之间潜在的新型相互作用提供了证据,其中之一是PDGF对IL-1受体的调节。此外,这些研究表明,由于PDGF和FGF对IL-1活性的影响,它们可能在结缔组织中发挥额外作用,包括在炎症过程中的间接作用。