Bachmann Anna, Metwally Nahla Galal, Allweier Johannes, Cronshagen Jakob, Del Pilar Martinez Tauler Maria, Murk Agnes, Roth Lisa Katharina, Torabi Hanifeh, Wu Yifan, Gutsmann Thomas, Bruchhaus Iris
Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Biology Department, University of Hamburg, 22601 Hamburg, Germany.
Microorganisms. 2022 Nov 29;10(12):2356. doi: 10.3390/microorganisms10122356.
infected erythrocytes (IEs) present erythrocyte membrane protein 1 proteins (EMP1s) on the cell surface, via which they cytoadhere to various endothelial cell receptors (ECRs) on the walls of human blood vessels. This prevents the parasite from passing through the spleen, which would lead to its elimination. Each isolate has about 60 different EMP1s acting as ligands, and at least 24 ECRs have been identified as interaction partners. Interestingly, in every parasite genome sequenced to date, at least 75% of the encoded EMP1s have a binding domain for the scavenger receptor CD36 widely distributed on host endothelial cells and many other cell types. Here, we discuss why the interaction between IEs and CD36 is optimal to maintain a finely regulated equilibrium that allows the parasite to multiply and spread while causing minimal harm to the host in most infections.
受感染的红细胞(IEs)在细胞表面呈现红细胞膜蛋白1(EMP1s),通过这些蛋白它们细胞黏附于人体血管壁上的各种内皮细胞受体(ECRs)。这可防止寄生虫通过脾脏,否则寄生虫会被清除。每个分离株约有60种不同的EMP1s作为配体,并且至少24种ECRs已被鉴定为相互作用伙伴。有趣的是,在迄今测序的每个寄生虫基因组中,至少75%的编码EMP1s具有针对广泛分布于宿主内皮细胞和许多其他细胞类型的清道夫受体CD36的结合域。在此,我们讨论为什么IEs与CD36之间的相互作用对于维持精细调节的平衡是最佳的,这种平衡使得寄生虫在大多数感染中能够繁殖和传播,同时对宿主造成最小的伤害。