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人类单核细胞清道夫受体在曼氏血吸虫杀伤中的潜在作用。

Potential role for scavenger receptors of human monocytes in the killing of Schistosoma mansoni.

作者信息

Xu X, Remold H G, Caulfield J P

机构信息

Department of Tropical Public Health, Harvard School of Public Health, Boston, Massachusetts.

出版信息

Am J Pathol. 1993 Mar;142(3):685-9.

Abstract

Human low-density lipoproteins (LDL) bind specifically and saturably to the surface of the trematode parasite, Schistosoma mansoni, in vitro. Here we have tested whether human monocytes process the bound LDL. Monocytes obtained by leukapheresis generate H2O2, kill schistosomula, and were seen here endocytosing fluorescently labeled human LDL that was bound to the surface of the parasites. Compounds known to inhibit uptake of LDL via the scavenger receptor, namely, acetylated LDL, polyinosinic acid, dextran sulfate, fucoidan, and polyvinyl sulfate, inhibited both endocytosis of LDL and cell-mediated killing. Non-functional analogs of these inhibitors, namely, polycytidylic acid and dextran, did not inhibit either endocytosis or killing. Monocytes obtained from whole blood after venipuncture neither killed the parasite nor endocytosed LDL from the worm surface. Thus, human monocyte killing of schistosomula may involve removal of LDL from the parasite surface via scavenger receptors.

摘要

人低密度脂蛋白(LDL)在体外能特异性且饱和性地结合到曼氏血吸虫这种吸虫寄生虫的表面。在此,我们测试了人单核细胞是否会处理结合的LDL。通过白细胞分离术获得的单核细胞会产生过氧化氢,杀死血吸虫幼虫,并且在此观察到它们会内吞结合在寄生虫表面的荧光标记人LDL。已知通过清道夫受体抑制LDL摄取的化合物,即乙酰化LDL、聚肌苷酸、硫酸葡聚糖、岩藻依聚糖和聚硫酸乙烯酯,既能抑制LDL的内吞作用,也能抑制细胞介导的杀伤作用。这些抑制剂的无功能类似物,即聚胞苷酸和葡聚糖,既不抑制内吞作用也不抑制杀伤作用。静脉穿刺后从全血中获得的单核细胞既不杀死寄生虫,也不会从虫体表面内吞LDL。因此,人单核细胞对血吸虫幼虫的杀伤作用可能涉及通过清道夫受体从寄生虫表面清除LDL。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bce/1886792/e576493e4ea9/amjpathol00075-0032-a.jpg

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