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巨噬细胞对被氧化剂修饰的红细胞的识别。

Macrophage recognition of the erythrocytes modified by oxidizing agents.

作者信息

Beppu M, Ochiai H, Kikugawa K

出版信息

Biochim Biophys Acta. 1987 Sep 14;930(2):244-53. doi: 10.1016/0167-4889(87)90037-1.

DOI:10.1016/0167-4889(87)90037-1
PMID:3620517
Abstract

Mouse erythrocytes modified by oxidizing agents (ADP/Fe3+, tert-butyl hydroperoxide and phenylhydrazine) were examined for recognition by autologous macrophages (cell adhesion and phagocytosis). Treatment of erythrocytes with ADP/Fe3+ resulted in lipid oxidation but no significant alterations in physical properties, and the treated cells were adherent to macrophages. When the lipid oxidation of erythrocytes was prevented by alpha-tocopherol, erythrocytes were not susceptible to macrophage adhesion, indicating that free radical reactions involving lipid oxidation are responsible for the formation or exposure of the membrane sites for the macrophage adhesion. Treatment of erythrocytes with tert-butyl hydroperoxide caused lipid oxidation and alterations in physical properties. Deformability and osmotic fragility of the treated cells were markedly low. Not only cell adhesion but subsequent phagocytosis of the treated cells by macrophages were observed. A similar effect was observed on treatment of erythrocytes with phenylhydrazine. The pronounced alterations in physical properties of the erythrocytes treated with tert-butyl hydroperoxide and phenylhydrazine may be responsible for the macrophage phagocytosis.

摘要

研究了经氧化剂(ADP/Fe3+、叔丁基过氧化氢和苯肼)修饰的小鼠红细胞被自体巨噬细胞识别的情况(细胞黏附和吞噬作用)。用ADP/Fe3+处理红细胞会导致脂质氧化,但物理性质无显著改变,且处理后的细胞可黏附于巨噬细胞。当用α-生育酚阻止红细胞的脂质氧化时,红细胞不易被巨噬细胞黏附,这表明涉及脂质氧化的自由基反应是巨噬细胞黏附的膜位点形成或暴露的原因。用叔丁基过氧化氢处理红细胞会导致脂质氧化和物理性质改变。处理后的细胞的变形性和渗透脆性明显降低。不仅观察到细胞黏附,还观察到巨噬细胞对处理后的细胞的后续吞噬作用。用苯肼处理红细胞也观察到类似效果。用叔丁基过氧化氢和苯肼处理的红细胞物理性质的显著改变可能是巨噬细胞吞噬作用的原因。

相似文献

1
Macrophage recognition of the erythrocytes modified by oxidizing agents.巨噬细胞对被氧化剂修饰的红细胞的识别。
Biochim Biophys Acta. 1987 Sep 14;930(2):244-53. doi: 10.1016/0167-4889(87)90037-1.
2
Lipid peroxidation and haemoglobin degradation in red blood cells exposed to t-butyl hydroperoxide. The relative roles of haem- and glutathione-dependent decomposition of t-butyl hydroperoxide and membrane lipid hydroperoxides in lipid peroxidation and haemolysis.暴露于叔丁基过氧化氢的红细胞中的脂质过氧化和血红蛋白降解。叔丁基过氧化氢和膜脂质氢过氧化物的血红素依赖性和谷胱甘肽依赖性分解在脂质过氧化和溶血中的相对作用。
Biochem J. 1983 Jun 15;212(3):759-72. doi: 10.1042/bj2120759.
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t-Butyl hydroperoxide-induced changes in the physicochemical properties of human erythrocytes.叔丁基过氧化氢诱导的人红细胞理化性质变化。
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Arch Biochem Biophys. 1994 Jul;312(1):189-97. doi: 10.1006/abbi.1994.1298.
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Radical-mediated damage to parasites and erythrocytes in Plasmodium vinckei infected mice after injection of t-butyl hydroperoxide.注射叔丁基过氧化氢后,对感染文氏疟原虫小鼠体内寄生虫和红细胞的自由基介导损伤。
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Macrophage recognition of periodate-treated erythrocytes: involvement of disulfide formation of the erythrocyte membrane proteins.巨噬细胞对高碘酸盐处理红细胞的识别:红细胞膜蛋白二硫键形成的参与。
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Free radical involvement in the oxidative phenomena induced by tert-butyl hydroperoxide in erythrocytes.自由基参与叔丁基过氧化氢诱导的红细胞氧化现象。
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Recognition of poly-N-acetyllactosaminyl saccharide chains on iron-oxidized erythrocytes by human monocytic leukemia cell line THP-1 differentiated into macrophages.人单核细胞白血病细胞系THP-1分化为巨噬细胞后对铁氧化红细胞上的多聚N-乙酰乳糖胺糖链的识别。
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Tumour promoter tert-butyl-hydroperoxide induces peroxynitrite formation in human erythrocytes.肿瘤促进剂叔丁基过氧化氢可诱导人红细胞中过氧亚硝酸盐的形成。
Anticancer Res. 1996 Sep-Oct;16(5A):2969-79.
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Prehemolytic effects of hydrogen peroxide and t-butylhydroperoxide on selected red cell properties.过氧化氢和叔丁基过氧化氢对选定红细胞特性的溶血前效应。
Biochim Biophys Acta. 1991 Jul 22;1066(2):193-200. doi: 10.1016/0005-2736(91)90186-c.

引用本文的文献

1
Recognition of oxidatively damaged erythrocytes by a macrophage receptor with specificity for oxidized low density lipoprotein.巨噬细胞通过对氧化型低密度脂蛋白具有特异性的受体识别氧化损伤的红细胞。
Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):3265-9. doi: 10.1073/pnas.91.8.3265.