Department of Developmental, Molecular & Chemical Biology, Tufts Universitygrid.429997.8, Boston, Massachusetts, USA.
Program in Pharmacology and Experimental Therapeutics, Graduate School of Biomedical Sciences, Tufts Universitygrid.429997.8, Boston, Massachusetts, USA.
Infect Immun. 2021 Sep 16;89(10):e0017821. doi: 10.1128/IAI.00178-21. Epub 2021 Jul 6.
The Chagas disease parasite Trypanosoma cruzi must extravasate to home in on susceptible cells residing in most tissues. It remains unknown how T. cruzi undertakes this crucial step of its life cycle. We hypothesized that the pathogen exploits the endothelial cell programming leukocytes use to extravasate to sites of inflammation. Transendothelial migration (TEM) starts after inflammatory cytokines induce E-selectin expression and P-selectin translocation on endothelial cells (ECs), enabling recognition by leukocyte ligands that engender rolling cell adhesion. Here, we show that T. cruzi upregulates E- and P-selectins in cardiac ECs to which it binds in a ligand-receptor fashion, whether under static or shear flow conditions. Glycoproteins isolated from T. cruzi (TcEx) specifically recognize P-selectin in a ligand-receptor interaction. As with leukocytes, binding of P-selectin to T. cruzi or TcEx requires sialic acid and tyrosine sulfate, which are pivotal for downstream migration across ECs and extracellular matrix proteins. Additionally, soluble selectins, which bind T. cruzi, block transendothelial migration dose dependently, implying that the pathogen bears selectin-binding ligand(s) that start transmigration. Furthermore, function-blocking antibodies against E- and P-selectins, which act on endothelial cells and not T. cruzi, are exquisite in preventing TEM. Thus, our results show that selectins can function as mediators of T. cruzi transendothelial transmigration, suggesting a pathogenic mechanism that allows homing in of the parasite on targeted tissues. As selectin inhibitors are sought-after therapeutic targets for autoimmune diseases and cancer metastasis, they may similarly represent a novel strategy for Chagas disease therapy.
克氏锥虫必须逸出到合适的细胞中,才能找到居住在大多数组织中的易感细胞。目前尚不清楚克氏锥虫如何完成其生命周期的这一关键步骤。我们假设病原体利用内皮细胞编程,使白细胞逸出到炎症部位。白细胞跨内皮迁移(TEM)始于炎症细胞因子诱导内皮细胞(EC)上 E-选择素和 P-选择素的表达和转位,使白细胞配体能够识别,从而引发滚动细胞黏附。在这里,我们表明,克氏锥虫在心脏 EC 中上调 E-和 P-选择素,以配体-受体的方式与其结合,无论是在静态还是剪切流条件下。从克氏锥虫中分离的糖蛋白(TcEx)特异性识别配体-受体相互作用中的 P-选择素。与白细胞一样,P-选择素与克氏锥虫或 TcEx 的结合需要唾液酸和酪氨酸硫酸盐,这对于跨内皮细胞和细胞外基质蛋白的下游迁移是至关重要的。此外,与克氏锥虫结合的可溶性选择素可依赖浓度阻断 TEM,这意味着病原体具有开始迁移的选择素结合配体。此外,针对内皮细胞而非克氏锥虫的 E-和 P-选择素的功能阻断抗体在阻止 TEM 方面非常出色。因此,我们的结果表明选择素可以作为克氏锥虫跨内皮迁移的介质,这表明了一种允许寄生虫定位于靶向组织的致病机制。由于选择素抑制剂是自身免疫性疾病和癌症转移的理想治疗靶点,它们可能同样代表了一种治疗恰加斯病的新策略。