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糖链和糖结合蛋白协调的自身免疫和感染中的免疫调节网络。

Immune regulatory networks coordinated by glycans and glycan-binding proteins in autoimmunity and infection.

机构信息

i3S - Institute for Research and Innovation in Health, University of Porto, 4200-135, Porto, Portugal.

ICBAS-School of Medicine and Biomedical Sciences, University of Porto, 4050-313, Porto, Portugal.

出版信息

Cell Mol Immunol. 2023 Oct;20(10):1101-1113. doi: 10.1038/s41423-023-01074-1. Epub 2023 Aug 15.

Abstract

The immune system is coordinated by an intricate network of stimulatory and inhibitory circuits that regulate host responses against endogenous and exogenous insults. Disruption of these safeguard and homeostatic mechanisms can lead to unpredictable inflammatory and autoimmune responses, whereas deficiency of immune stimulatory pathways may orchestrate immunosuppressive programs that contribute to perpetuate chronic infections, but also influence cancer development and progression. Glycans have emerged as essential components of homeostatic circuits, acting as fine-tuners of immunological responses and potential molecular targets for manipulation of immune tolerance and activation in a wide range of pathologic settings. Cell surface glycans, present in cells, tissues and the extracellular matrix, have been proposed to serve as "self-associated molecular patterns" that store structurally relevant biological data. The responsibility of deciphering this information relies on different families of glycan-binding proteins (including galectins, siglecs and C-type lectins) which, upon recognition of specific carbohydrate structures, can recalibrate the magnitude, nature and fate of immune responses. This process is tightly regulated by the diversity of glycan structures and the establishment of multivalent interactions on cell surface receptors and the extracellular matrix. Here we review the spatiotemporal regulation of selected glycan-modifying processes including mannosylation, complex N-glycan branching, core 2 O-glycan elongation, LacNAc extension, as well as terminal sialylation and fucosylation. Moreover, we illustrate examples that highlight the contribution of these processes to the control of immune responses and their integration with canonical tolerogenic pathways. Finally, we discuss the power of glycans and glycan-binding proteins as a source of immunomodulatory signals that could be leveraged for the treatment of autoimmune inflammation and chronic infection.

摘要

免疫系统由一个复杂的刺激和抑制回路网络协调,该网络调节宿主对内外源刺激的反应。这些保护和内稳机制的破坏可导致不可预测的炎症和自身免疫反应,而免疫刺激途径的缺乏可能协调免疫抑制程序,这些程序有助于慢性感染的持续,但也影响癌症的发展和进展。糖被已成为内稳回路的重要组成部分,作为调节免疫反应的精细调节剂,并且是在广泛的病理环境中操纵免疫耐受和激活的潜在分子靶标。存在于细胞、组织和细胞外基质中的细胞表面糖链被提出作为“自身相关分子模式”,它们存储结构上相关的生物学数据。解读这些信息的责任依赖于不同的糖结合蛋白家族(包括半乳糖凝集素、Siglec 和 C 型凝集素),这些蛋白在识别特定的碳水化合物结构后,可以重新校准免疫反应的幅度、性质和命运。这个过程受到糖结构的多样性和细胞表面受体和细胞外基质上多价相互作用的建立的严格调控。在这里,我们综述了选定的糖修饰过程的时空调控,包括甘露糖基化、复杂 N-糖链分支、核心 2 O-糖链延伸、LacNAc 延伸以及末端唾液酸化和岩藻糖化。此外,我们举例说明了这些过程对免疫反应控制的贡献以及它们与经典耐受途径的整合。最后,我们讨论了糖和糖结合蛋白作为免疫调节信号源的潜力,这些信号源可用于治疗自身免疫炎症和慢性感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cab/10541879/82a5a354f0d2/41423_2023_1074_Fig1_HTML.jpg

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