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接种于单克隆抗体包被的免疫复合物底物上的小鼠腹腔巨噬细胞的吞噬作用:不同IgG亚类复合物对Fc受体功能的影响。

Phagocytosis by mouse peritoneal macrophages plated on monoclonal antibody-coated immune complex-substrates: effects of complexes of different IgG subclasses on Fc receptor functions.

作者信息

Sung S S

出版信息

J Immunol. 1985 Sep;135(3):1981-6.

PMID:4020136
Abstract

Macrophages plated on immune complex-coated substrates of different mouse IgG subclasses were examined for their capacities to phagocytose sheep red blood cells (SRBC) coated with monoclonal antibodies (MAb) of various IgG subclasses. IgG2a-and IgG2b-coated substrates abrogated macrophage phagocytosis of particles coated with any of the four mouse IgG subclasses. These results were confirmed by the use of two MAb of each of the IgG2a and IgG2b subclasses, with one of the MAb specific for dinitrophenyl groups and the others for SRBC. IgG3-coated substrates reduced the macrophage uptake of IgG2a-but not IgG2b-coated particles. Rabbit IgG-coated substrates ablated the uptake of SRBC coated with all mouse IgG subclasses. Resident and thioglycollate-elicited macrophages showed similar phagocytosis reduction when plated on these immune complexes. The phagocytosis of complement-coated particles was not affected by these IgG-coated substrates. Macrophages plated on both IgG2a-and IgG2b-coated substrates showed reduced immunofluorescence staining by an anti-IgG2b Fc receptor (FcR) Ab, 2.4G2 and reduced E(IgG2a) and E(IgG2b) binding. The results show that substrates coated with various IgG subclasses can abrogate phagocytosis mediated by FcR that do not have binding specificity for the substrate-immobilized Fc ligand, and suggest that the three classes of mouse FcR co-modulate.

摘要

研究了接种在不同小鼠IgG亚类免疫复合物包被底物上的巨噬细胞对包被有各种IgG亚类单克隆抗体(MAb)的绵羊红细胞(SRBC)的吞噬能力。IgG2a和IgG2b包被的底物消除了巨噬细胞对包被有任何四种小鼠IgG亚类的颗粒的吞噬作用。使用IgG2a和IgG2b亚类的两种MAb证实了这些结果,其中一种MAb对二硝基苯基基团具有特异性,另一种对SRBC具有特异性。IgG3包被的底物减少了巨噬细胞对IgG2a包被但不是IgG2b包被颗粒的摄取。兔IgG包被的底物消除了对包被有所有小鼠IgG亚类的SRBC的摄取。当接种在这些免疫复合物上时,驻留巨噬细胞和巯基乙酸诱导的巨噬细胞显示出相似的吞噬作用降低。补体包被颗粒的吞噬作用不受这些IgG包被底物的影响。接种在IgG2a和IgG2b包被底物上的巨噬细胞通过抗IgG2b Fc受体(FcR)抗体2.4G2显示出免疫荧光染色减少,以及E(IgG2a)和E(IgG2b)结合减少。结果表明,包被有各种IgG亚类的底物可以消除由对底物固定的Fc配体没有结合特异性的FcR介导的吞噬作用,并提示三类小鼠FcR共同调节。

相似文献

1
Phagocytosis by mouse peritoneal macrophages plated on monoclonal antibody-coated immune complex-substrates: effects of complexes of different IgG subclasses on Fc receptor functions.接种于单克隆抗体包被的免疫复合物底物上的小鼠腹腔巨噬细胞的吞噬作用:不同IgG亚类复合物对Fc受体功能的影响。
J Immunol. 1985 Sep;135(3):1981-6.
2
Mouse peritoneal macrophages plated on mannan- and horseradish peroxidase-coated substrates lose the ability to phagocytose by their Fc receptors.接种在甘露聚糖和辣根过氧化物酶包被底物上的小鼠腹腔巨噬细胞失去了通过其Fc受体进行吞噬的能力。
J Immunol. 1985 Jun;134(6):3712-7.
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Fc receptors on mouse neutrophils and eosinophils: antigenic characteristics, isotype specificity and relative cell membrane density measured by flow cytometry.小鼠中性粒细胞和嗜酸性粒细胞上的Fc受体:抗原特性、同种型特异性以及通过流式细胞术测量的相对细胞膜密度
Immunology. 1985 May;55(1):125-33.
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IgG1 and IgG2b share the Fc receptor on mouse macrophages.IgG1和IgG2b在小鼠巨噬细胞上共享Fc受体。
J Immunol. 1980 Aug;125(2):631-3.
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T cell activation by anti-T3 antibodies: comparison of IgG1 and IgG2b switch variants and direct evidence for accessory function of macrophage Fc receptors.抗T3抗体激活T细胞:IgG1和IgG2b转换变体的比较以及巨噬细胞Fc受体辅助功能的直接证据。
Eur J Immunol. 1986 May;16(5):478-86. doi: 10.1002/eji.1830160503.
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Selective modulation of two human monocyte Fc receptors for IgG by immobilized immune complexes.固定化免疫复合物对人单核细胞两种IgG Fc受体的选择性调节
J Immunol. 1988 May 15;140(10):3515-21.
7
All classes of murine IgG antibody mediate macrophage phagocytosis and lysis of erythrocytes.所有类别的小鼠IgG抗体都介导巨噬细胞对红细胞的吞噬作用和裂解作用。
J Immunol. 1980 Nov;125(5):1885-8.
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Binding of human C-reactive protein to mouse macrophages is mediated by distinct receptors.人C反应蛋白与小鼠巨噬细胞的结合是由不同的受体介导的。
J Immunol. 1989 Apr 1;142(7):2384-92.
9
Exogenous C1q reconstitutes resident but not inflammatory mouse peritoneal macrophages for Fc receptor-dependent cellular cytotoxicity and phagocytosis. Relationship to endogenous C1q availability.外源性C1q可重构驻留而非炎性小鼠腹腔巨噬细胞,以实现Fc受体依赖性细胞毒性和吞噬作用。与内源性C1q可用性的关系。
J Immunol. 1989 Nov 15;143(10):3250-7.
10
A new Fc receptor on mouse macrophages binding IgG3.小鼠巨噬细胞上一种新的结合IgG3的Fc受体。
J Exp Med. 1981 Mar 1;153(3):514-9. doi: 10.1084/jem.153.3.514.

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