Proost P, De Wolf-Peeters C, Conings R, Opdenakker G, Billiau A, Van Damme J
Rega Institute for Medical Research, University of Leuven, Belgium.
J Immunol. 1993 Feb 1;150(3):1000-10.
Stimulated human osteosarcoma cells (MG-63) were used as a source of granulocyte chemotactic protein (GCP). In addition to the previously isolated GCP-1/IL-8, natural forms of GRO alpha, GRO gamma, and IP-10 were purified and identified by amino acid sequence analysis. Further, a novel GCP, GCP-2, was isolated in its natural form (6 kDa) and was found to be structurally related to the other members of the IL-8 family. GRO alpha, IP-10, and GCP-2 showed heterogeneity, in that several forms of each protein were recovered. These differed in truncation at the amino terminus. Reverse phase HPLC allowed us to separate four such different forms of GCP-2. These tumor-derived factors were compared in granulocyte activation and chemotaxis assays. IL-8 induced neutrophil gelatinase B release at 2 nM, but GRO alpha and GCP-2 showed a 5- to 10-fold lower specific activity. When the migration of granulocytes through polycarbonate micropore membranes was measured, GCP-2 and GRO alpha had a maximal chemotactic index comparable to that of IL-8. The minimal effective dose for GCP-2 and GRO alpha was 3 to 10 nM, whereas the specific activity of IL-8 was at least 10-fold higher. IP-10 was not active in this assay at doses up to 100 nM. Finally, in vivo chemotaxis was measured by using granulocyte recruitment in the rabbit skin model. After intradermal injection of 200 ng/site, GCP-2 provoked a significant granulocyte infiltration, albeit to a lesser extent than did IL-8 and GRO alpha. GCP-2 did not attract monocytes in vivo nor did it induce the cells in vitro to migrate or to produce enzyme. In conclusion, this study reveals a new member of the IL-8 family and shows that these related inflammatory mediators possess different potencies and efficacies towards granulocytes.
刺激后的人骨肉瘤细胞(MG-63)被用作粒细胞趋化蛋白(GCP)的来源。除了先前分离出的GCP-1/IL-8,GROα、GROγ和IP-10的天然形式也通过氨基酸序列分析得以纯化和鉴定。此外,一种新型GCP,即GCP-2,以其天然形式(6 kDa)被分离出来,并被发现与IL-8家族的其他成员在结构上相关。GROα、IP-10和GCP-2表现出异质性,每种蛋白质都回收得到了几种形式。这些形式在氨基末端的截短情况有所不同。反相高效液相色谱使我们能够分离出四种这样不同形式的GCP-2。在粒细胞活化和趋化试验中对这些肿瘤衍生因子进行了比较。IL-8在2 nM时诱导中性粒细胞明胶酶B释放,但GROα和GCP-2的比活性低5至10倍。当测量粒细胞通过聚碳酸酯微孔膜的迁移时,GCP-2和GROα的最大趋化指数与IL-8相当。GCP-2和GROα的最小有效剂量为3至10 nM,而IL-8的比活性至少高10倍。在该试验中,剂量高达100 nM时IP-10无活性。最后,通过兔皮肤模型中的粒细胞募集来测量体内趋化作用。在皮内注射200 ng/部位后,GCP-2引起了显著的粒细胞浸润,尽管程度比IL-8和GROα小。GCP-2在体内不吸引单核细胞,在体外也不诱导细胞迁移或产生酶。总之,本研究揭示了IL-8家族的一个新成员,并表明这些相关的炎症介质对粒细胞具有不同的效力和功效。