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人单核细胞衍生的巨噬细胞会被曼氏血吸虫的童虫裂解,并且在用γ干扰素激活后无法杀死该寄生虫。

Human monocyte-derived macrophages are lysed by schistosomula of Schistosoma mansoni and fail to kill the parasite after activation with interferon gamma.

作者信息

Remold H G, Mednis A, Hein A, Caulfield J P

机构信息

Department of Medicine and Pathology, Harvard Medical School, Boston, Massachusetts.

出版信息

Am J Pathol. 1988 Apr;131(1):146-55.

Abstract

In this study was examined the interaction between schistosomula of Schistosoma mansoni and human monocyte-derived macrophages activated with interferon gamma (IFN-gamma). Peripheral blood monocytes were matured for 6 days and activated by further culture with IFN-gamma (600 U/ml). These IFN-gamma-treated monocyte-derived macrophages are cytotoxic for the tumor cell line K562, which is not killed by nonactivated monocyte-derived macrophages. Activated monocyte-derived macrophages were incubated with schistosomula at ratios of 10(3):1 and 10(4):1 in the presence of serum pooled from patients with schistosomiasis. This antiserum promoted an increased adherence of cells to the parasite. However, the activated monocyte-derived macrophages failed to kill the schistosomula under all conditions tested. On the contrary, the monocyte-derived macrophages were killed by schistosomula in a time-dependent and antibody-dependent manner, which was most evident at a lower effector/target ratio, 200:1. Electron microscopy showed that monocyte-derived macrophages were lysed on the surface of schistosomula. Further, both monocyte-derived macrophages and contaminating blood platelets fused with the parasite surface membrane, so that the cell plasma membrane and the outer tegumental membrane formed a hybrid membrane. The results indicate that matured human monocyte-derived macrophages activated by IFN-gamma are unable to kill schistosomula. Instead, the effector cells fuse with the parasites and are lysed by them.

摘要

本研究检测了曼氏血吸虫童虫与经γ干扰素(IFN-γ)激活的人单核细胞衍生巨噬细胞之间的相互作用。外周血单核细胞成熟6天,再用IFN-γ(600 U/ml)进一步培养使其激活。这些经IFN-γ处理的单核细胞衍生巨噬细胞对肿瘤细胞系K562具有细胞毒性,而未激活的单核细胞衍生巨噬细胞不能杀死该肿瘤细胞系。在存在血吸虫病患者混合血清的情况下,将激活的单核细胞衍生巨噬细胞与童虫按10(3):1和10(4):1的比例孵育。这种抗血清促进了细胞与寄生虫的黏附增加。然而,在所有测试条件下,激活的单核细胞衍生巨噬细胞均未能杀死童虫。相反,单核细胞衍生巨噬细胞以时间依赖性和抗体依赖性方式被童虫杀死,在较低的效应细胞/靶细胞比例200:1时最为明显。电子显微镜显示单核细胞衍生巨噬细胞在童虫表面被裂解。此外,单核细胞衍生巨噬细胞和污染的血小板均与寄生虫表面膜融合,从而使细胞质膜和外皮层膜形成了混合膜。结果表明,经IFN-γ激活的成熟人单核细胞衍生巨噬细胞无法杀死童虫。相反,效应细胞与寄生虫融合并被其裂解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f9/1880563/63ffd1edbf05/amjpathol00133-0157-a.jpg

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