Goerdeler Felix, Seeberger Peter H, Moscovitz Oren
Department of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.
Institute of Chemistry and Biochemistry, Freie Universität Berlin, Berlin, Germany.
Front Microbiol. 2021 Jul 16;12:712538. doi: 10.3389/fmicb.2021.712538. eCollection 2021.
parasites cause malaria disease, one of the leading global health burdens for humanity, infecting hundreds of millions of people each year. Different glycans on the parasite and the host cell surface play significant roles in both malaria pathogenesis and host defense mechanisms. So far, only small, truncated and -glycans have been identified in species. In contrast, complex glycosylphosphatidylinositol (GPI) glycolipids are highly abundant on the parasite's cell membrane and are essential for its survival. Moreover, the parasites express lectins that bind and exploit the host cell surface glycans for different aspects of the parasite life cycle, such as adherence, invasion, and evasion of the host immune system. In parallel, the host cell glycocalyx and lectin expression serve as the first line of defense against parasites and directly dictate susceptibility to Plasmodium infection. This review provides an overview of the glycobiology involved in -host interactions and its contribution to malaria pathogenesis. Recent findings are presented and evaluated in the context of potential therapeutic exploitation.
寄生虫引发疟疾,这是全球人类主要的健康负担之一,每年感染数亿人。寄生虫和宿主细胞表面的不同聚糖在疟疾发病机制和宿主防御机制中都发挥着重要作用。到目前为止,在该物种中仅鉴定出小的、截短的聚糖。相比之下,复杂的糖基磷脂酰肌醇(GPI)糖脂在寄生虫细胞膜上高度丰富,对其生存至关重要。此外,寄生虫表达凝集素,这些凝集素结合并利用宿主细胞表面聚糖来完成寄生虫生命周期的不同环节,如黏附、入侵和逃避宿主免疫系统。同时,宿主细胞糖萼和凝集素表达作为抵御该寄生虫的第一道防线,直接决定对疟原虫感染的易感性。本综述概述了疟原虫与宿主相互作用中涉及的糖生物学及其对疟疾发病机制的贡献。在潜在治疗应用的背景下展示并评估了最新研究结果。