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抗I区同种异体抗体可阻断巨噬细胞与白色葡萄球菌的结合。

Macrophage binding of Staphylococcus albus is blocked by anti I-region alloantibody.

作者信息

Stewart J, Glass E J, Weir D M

出版信息

Nature. 1982 Aug 26;298(5877):852-4. doi: 10.1038/298852a0.

DOI:10.1038/298852a0
PMID:6955595
Abstract

Cell surface interactions involving carbohydrate may be important in immune recognition. Previous work from this laboratory has demonstrated the presence of 'lectin-like' receptors on mouse peritoneal macrophages that bind bacteria by means of their cell wall sugars. Others have shown that Ia molecules can bind antigen at specific sites which may be involved in presenting antigen to the immune system and recent work has shown that these molecules can carry carbohydrate determinants. It has also been found that human Ia molecules can bind to carbohydrates. As cell surface carbohydrate recognition mechanisms have been implicated in other immune interactions sugar-specific receptors may have a function in self--non-self recognition. We show here that the binding of the bacterium Staphylococcus albus to mouse peritoneal macrophages was inhibited by various conventional and monoclonal antibodies to Ia antigens suggesting that an I-region gene product may be associated with the binding of unopsonized bacteria.

摘要

涉及碳水化合物的细胞表面相互作用在免疫识别中可能很重要。本实验室先前的研究表明,小鼠腹腔巨噬细胞上存在“凝集素样”受体,该受体通过细菌细胞壁糖类结合细菌。其他人已经表明,Ia分子可以在特定部位结合抗原,这些部位可能参与将抗原呈递给免疫系统,最近的研究表明这些分子可以携带碳水化合物决定簇。还发现人类Ia分子可以与碳水化合物结合。由于细胞表面碳水化合物识别机制与其他免疫相互作用有关,糖特异性受体可能在自身-非自身识别中发挥作用。我们在此表明,各种针对Ia抗原的传统抗体和单克隆抗体可抑制白色葡萄球菌与小鼠腹腔巨噬细胞的结合,这表明I区基因产物可能与未调理细菌的结合有关。

相似文献

1
Macrophage binding of Staphylococcus albus is blocked by anti I-region alloantibody.抗I区同种异体抗体可阻断巨噬细胞与白色葡萄球菌的结合。
Nature. 1982 Aug 26;298(5877):852-4. doi: 10.1038/298852a0.
2
Lactoferrin acts on I-A and I-E/C antigen+ subpopulations of mouse peritoneal macrophages in the absence of T lymphocytes and other cell types to inhibit production of granulocyte-macrophage colony stimulatory factors in vitro.乳铁蛋白在无T淋巴细胞和其他细胞类型的情况下作用于小鼠腹腔巨噬细胞的I-A和I-E/C抗原阳性亚群,以在体外抑制粒细胞-巨噬细胞集落刺激因子的产生。
J Immunol. 1984 Jul;133(1):306-14.
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The molecular basis of T helper cell function--I. Allotype- and MHC-linked determinants on antigen-specific, H-2-restricted T cell lines, hybridomas and lymphomas.
Mol Immunol. 1984 Oct;21(10):915-28. doi: 10.1016/0161-5890(84)90148-2.
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Functional diversity of Ia epitopes on macrophages.巨噬细胞上Ia抗原决定簇的功能多样性。
Eur J Immunol. 1987 Jul;17(7):915-9. doi: 10.1002/eji.1830170704.
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Lymphokine enhances the expression and synthesis of Ia antigens on cultured mouse peritoneal macrophages.淋巴因子可增强培养的小鼠腹腔巨噬细胞上Ia抗原的表达与合成。
J Exp Med. 1980 Nov 1;152(5):1248-61. doi: 10.1084/jem.152.5.1248.
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Expression of Ia antigens on macrophages is reduced after stimulation with homologous C3b.
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Membrane changes in murine macrophages after in-vivo stimulation and activation.体内刺激和激活后小鼠巨噬细胞的膜变化。
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Wheat germ agglutinin potentiates uptake of bacteria by murine peritoneal macrophages.小麦胚凝集素增强小鼠腹腔巨噬细胞对细菌的摄取。
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Characterization of two distinct primary T cell populations that secrete interleukin 2 upon recognition of class I or class II major histocompatibility antigens.两种不同的初始T细胞群体的特征,这两种群体在识别I类或II类主要组织相容性抗原后会分泌白细胞介素2 。
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Monoclonal antibodies to mouse MHC antigens. I. Serologic characterization of ten anti-H-2 and anti-Ia reagents.针对小鼠主要组织相容性复合体(MHC)抗原的单克隆抗体。I. 十种抗H-2和抗Ia试剂的血清学特征
Immunogenetics. 1984;19(2):169-73. doi: 10.1007/BF00387861.

引用本文的文献

1
Macrophage signal recognition.巨噬细胞信号识别。
Agents Actions. 1984 Aug;15(1-2):2-11. doi: 10.1007/BF01966938.
2
Membrane changes in murine macrophages after in-vivo stimulation and activation.体内刺激和激活后小鼠巨噬细胞的膜变化。
Immunology. 1983 Sep;50(1):165-73.
3
Altered immune function in alloxan-induced diabetes in mice.小鼠中四氧嘧啶诱导的糖尿病的免疫功能改变。
Clin Exp Immunol. 1986 Sep;65(3):614-21.
4
Impairment of monocyte "lectin-like" receptor activity in type 1 (insulin-dependent) diabetic patients.1型(胰岛素依赖型)糖尿病患者单核细胞“凝集素样”受体活性受损。
Diabetologia. 1987 Apr;30(4):228-31. doi: 10.1007/BF00270420.