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白细胞功能反应中的Fcγ受体异质性

Fcγ Receptor Heterogeneity in Leukocyte Functional Responses.

作者信息

Rosales Carlos

机构信息

Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México , Ciudad de México , Mexico.

出版信息

Front Immunol. 2017 Mar 20;8:280. doi: 10.3389/fimmu.2017.00280. eCollection 2017.

DOI:10.3389/fimmu.2017.00280
PMID:28373871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5357773/
Abstract

Antibodies participate in defense of the organism from all types of pathogens, including viruses, bacteria, fungi, and protozoa. IgG antibodies recognize their associated antigen their two Fab portions and are in turn recognized though their Fc portion by specific Fcγ receptors (FcγRs) on the membrane of immune cells. Multiple types and polymorphic variants of FcγR exist. These receptors are expressed in many cells types and are also redundant in inducing cell responses. Crosslinking of FcγR on the surface of leukocytes activates several effector functions aimed toward the destruction of pathogens and the induction of an inflammatory response. In the past few years, new evidence on how the particular IgG subclass and the glycosylation pattern of the antibody modulate the IgG-FcγR interaction has been presented. Despite these advances, our knowledge of what particular effector function is activated in a certain cell and in response to a specific type of FcγR remains very limited today. On one hand, each immune cell could be programmed to perform a particular cell function after FcγR crosslinking. On the other, each FcγR could activate a particular signaling pathway leading to a unique cell response. In this review, I describe the main types of FcγRs and our current view of how particular FcγRs activate various signaling pathways to promote unique leukocyte functions.

摘要

抗体参与机体抵御各类病原体的防御过程,这些病原体包括病毒、细菌、真菌和原生动物。IgG抗体通过其两个Fab部分识别相关抗原,并通过其Fc部分被免疫细胞膜上的特异性Fcγ受体(FcγRs)识别。FcγR存在多种类型和多态性变体。这些受体在多种细胞类型中表达,并且在诱导细胞反应方面具有冗余性。白细胞表面FcγR的交联激活了多种效应功能,旨在破坏病原体并诱导炎症反应。在过去几年中,已经有关于特定IgG亚类和抗体糖基化模式如何调节IgG-FcγR相互作用的新证据。尽管取得了这些进展,但我们目前对于在特定细胞中以及针对特定类型的FcγR激活何种特定效应功能的了解仍然非常有限。一方面,每个免疫细胞在FcγR交联后可能被编程执行特定的细胞功能。另一方面,每个FcγR可能激活特定的信号通路,导致独特的细胞反应。在这篇综述中,我描述了FcγR的主要类型以及我们目前对于特定FcγR如何激活各种信号通路以促进独特白细胞功能的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/b8be26cf1642/fimmu-08-00280-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/413758d83e12/fimmu-08-00280-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/49fb6d0c508c/fimmu-08-00280-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/95f9479f4852/fimmu-08-00280-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/cd94ddcbc5e0/fimmu-08-00280-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/ed51c83168bf/fimmu-08-00280-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/b8be26cf1642/fimmu-08-00280-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/413758d83e12/fimmu-08-00280-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/49fb6d0c508c/fimmu-08-00280-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/95f9479f4852/fimmu-08-00280-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/cd94ddcbc5e0/fimmu-08-00280-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/ed51c83168bf/fimmu-08-00280-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fc/5357773/b8be26cf1642/fimmu-08-00280-g006.jpg

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The FcγR/IgG Interaction as Target for the Treatment of Autoimmune Diseases.
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Machine Learning and Experiments Revealed Key Genes Related to PANoptosis Linked to Drug Prediction and Immune Landscape in Spinal Cord Injury.机器学习与实验揭示了与脊髓损伤中全程序性坏死相关的关键基因,这些基因与药物预测和免疫格局有关。
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