Brittingham A, Chen G, McGwire B S, Chang K P, Mosser D M
Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
Infect Immun. 1999 Sep;67(9):4477-84. doi: 10.1128/IAI.67.9.4477-4484.1999.
The most abundant protein on the surface of the promastigote form of the protozoan parasites Leishmania spp. is a 63-kDa molecule, designated gp63 or leishmanolysin. Because gp63 has been shown to possess fibronectin-like properties, we examined the interaction of gp63 with the cellular receptors for fibronectin. We measured the direct binding of Leishmania to human macrophages or to transfected mammalian cells expressing human fibronectin receptors. Leishmania expressing gp63 exhibited modest but reproducible adhesion to human macrophages and to transfected CHO cells expressing alpha4/beta1 fibronectin receptors. In both cases, this interaction depended on gp63 but occurred independently of the SRYD sequence of gp63, because parasites expressing gp63 with a mutated SRYD sequence bound to macrophages and alpha4/beta1 receptor-expressing cells as well as did wild-type parasites. The contribution of gp63 to parasite adhesion was more pronounced when the assays were performed in the presence of complement, suggesting that the receptors for complement and fibronectin may cooperate to mediate the efficient adhesion of parasites to macrophages. The interaction of gp63 with fibronectin receptors may also play an important role in parasite internalization by macrophages. Erythrocytes to which gp63 was cross-linked were efficiently phagocytized by macrophages, whereas control erythrocytes opsonized with complement alone bound to macrophages but remained peripherally attached to the outside of the cell. Similarly, parasites expressing wild-type gp63 were rapidly and efficiently phagocytized by resting macrophages, whereas parasites lacking gp63 were internalized more slowly. This rapid internalization of gp63-expressing parasites was dependent on the beta1 integrins, because pretreatment of macrophages with monoclonal antibodies to the beta1 integrins decreased the internalization of gp63-expressing parasites. These observations indicate that complement receptors are the primary mediators of parasite adhesion; however, maximal parasite adhesion and internalization may require the participation of the beta1 integrins, which recognize fibronectin-like molecules such as gp63 on the surface of the parasite.
原生动物寄生虫利什曼原虫前鞭毛体形式表面最丰富的蛋白质是一种63 kDa的分子,称为gp63或利什曼溶素。由于已证明gp63具有纤连蛋白样特性,我们研究了gp63与纤连蛋白细胞受体的相互作用。我们测量了利什曼原虫与人巨噬细胞或表达人纤连蛋白受体的转染哺乳动物细胞的直接结合。表达gp63的利什曼原虫对人巨噬细胞和表达α4/β1纤连蛋白受体的转染CHO细胞表现出适度但可重复的粘附。在这两种情况下,这种相互作用依赖于gp63,但独立于gp63的SRYD序列发生,因为表达具有突变SRYD序列的gp63的寄生虫与巨噬细胞和表达α4/β1受体的细胞结合的情况与野生型寄生虫一样。当在补体存在下进行测定时,gp63对寄生虫粘附的贡献更为明显,这表明补体和纤连蛋白的受体可能协同介导寄生虫与巨噬细胞的有效粘附。gp63与纤连蛋白受体的相互作用在巨噬细胞将寄生虫内化过程中也可能起重要作用。与gp63交联的红细胞被巨噬细胞有效吞噬,而仅用补体调理的对照红细胞与巨噬细胞结合但仍外周附着于细胞外。同样,表达野生型gp63的寄生虫被静息巨噬细胞快速有效地吞噬,而缺乏gp63的寄生虫内化较慢。表达gp63的寄生虫的这种快速内化依赖于β1整合素,因为用针对β1整合素的单克隆抗体预处理巨噬细胞会降低表达gp63的寄生虫的内化。这些观察结果表明补体受体是寄生虫粘附的主要介质;然而,最大程度的寄生虫粘附和内化可能需要β1整合素的参与,β1整合素可识别寄生虫表面的纤连蛋白样分子如gp63。