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红色诺卡氏菌细胞壁骨架对小鼠腹腔巨噬细胞功能特性的体内激活作用

In vivo activation of functional properties in mouse peritoneal macrophages by Nocardia rubra cell wall skeleton.

作者信息

Mine Y, Watanabe Y, Tawara S, Nonoyama S, Yokota Y, Kikuchi H

出版信息

Arzneimittelforschung. 1986 Nov;36(11):1651-5.

PMID:3028437
Abstract

Exudative cells in the peritoneal cavity of mice, particularly polymorphonuclear leukocytes significantly increased 1 day after intraperitoneal injection of Nocardia rubra cell wall skeleton (N-CWS). Macrophages and lymphocytes significantly increased 4 to 7 days after injection. N-CWS also enhanced peritoneal macrophage functions such as phagocytosis of latex particles, production of superoxide anion, production and secretion of lysosomal enzymes such as beta-glucuronidase, lysozyme and acid phosphatase, phagocytosis and intracellular killing of bacteria, and in vitro chemotaxis. The phagocytic function of the reticuloendothelial system was also enhanced. These results indicate that macrophages were activated in vivo by N-CWS.

摘要

给小鼠腹腔注射红色诺卡氏菌细胞壁骨架(N-CWS)1天后,小鼠腹腔内的渗出细胞,尤其是多形核白细胞显著增加。注射后4至7天,巨噬细胞和淋巴细胞显著增加。N-CWS还增强了腹腔巨噬细胞的功能,如吞噬乳胶颗粒、产生超氧阴离子、产生和分泌溶酶体酶(如β-葡萄糖醛酸酶、溶菌酶和酸性磷酸酶)、吞噬和细胞内杀灭细菌以及体外趋化性。网状内皮系统的吞噬功能也得到增强。这些结果表明,N-CWS在体内激活了巨噬细胞。

相似文献

1
In vivo activation of functional properties in mouse peritoneal macrophages by Nocardia rubra cell wall skeleton.红色诺卡氏菌细胞壁骨架对小鼠腹腔巨噬细胞功能特性的体内激活作用
Arzneimittelforschung. 1986 Nov;36(11):1651-5.
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Effect of Nocardia rubra cell wall skeleton on murine interferon production in vitro.
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Effector mechanism in concomitant immunity potentiated by intratumoral injection of Nocardia rubra cell wall skeleton.瘤内注射红色诺卡氏菌细胞壁骨架增强伴随免疫中的效应机制。
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Killing of tumor cells in vitro by macrophages from mice given injections of squalene-treated cell wall skeleton of Nocardia rubra.给小鼠注射经角鲨烯处理的红色诺卡氏菌细胞壁骨架后,从小鼠体内获取的巨噬细胞在体外对肿瘤细胞的杀伤作用。
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Effect of Nocardia rubra cell wall skeleton on humoral and cellular factors related to immune response in mice and guinea pigs.诺卡氏菌细胞壁骨架对小鼠和豚鼠免疫反应相关体液及细胞因子的影响。
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Jpn J Cancer Res. 1985 May;76(5):400-13.

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