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Development of a pHrodo-Based Assay for the Assessment of In Vitro and In Vivo Erythrophagocytosis during Experimental Trypanosomosis

机译:一种基于pHrodo的检测方法的发展,用于在实验锥虫病期间评估体内和体内的红细胞吞噬作用

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Extracellular trypanosomes can cause a wide range of diseases and pathological complications in a broad range of mammalian hosts. One common feature of trypanosomosis is the occurrence of anemia, caused by an imbalance between erythropoiesis and red blood cell clearance of aging erythrocytes. In murine models for T. brucei trypanosomosis, anemia is marked by a very sudden non-hemolytic loss of RBCs during the first-peak parasitemia control, followed by a short recovery phase and the subsequent gradual occurrence of an ever-increasing level of anemia. Using a newly developed quantitative pHrodo based in vitro erythrophagocytosis assay, combined with FACS-based ex vivo and in vivo results, we show that activated liver monocytic cells and neutrophils as well as activated splenic macrophages are the main cells involved in the occurrence of the early-stage acute anemia. In addition, we show that trypanosomosis itself leads to a rapid alteration of RBC membrane stability, priming the cells for accelerated phagocytosis.
机译:细胞外锥虫可在多种哺乳动物宿主中引起多种疾病和病理并发症。锥虫病的一个共同特征是贫血的发生,这是由于红细胞生成和衰老的红细胞清除红血球之间的不平衡引起的。在布鲁氏锥虫锥虫病的小鼠模型中,贫血的特征是在控制首峰寄生虫血症期间,RBC突然非溶血性丧失,随后恢复期很短,随后逐渐发生贫血程度不断增加。使用新开发的基于定量pHrodo的体外红细胞吞噬试验,结合基于FACS的离体和体内结果,我们显示活化的肝单核细胞和中性粒细胞以及活化的脾巨噬细胞是参与早期发生的主要细胞期急性贫血。此外,我们表明锥虫病本身会导致RBC膜稳定性的快速改变,引发细胞加速吞噬作用。

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