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来自[具体来源未明确]的脂多糖结构:免疫识别的化学视角

Structure of the Lipopolysaccharide from : A Chemical Perspective on Immune Recognition.

作者信息

Nieto-Fabregat Ferran, Mercogliano Marcello, Cangiano Alessandro, Vitiello Giuseppe, Andretta Emanuela, Clifton Luke A, Vanacore Adele, Buono Lorena, Campanero-Rhodes María Asunción, Solís Dolores, Di Carluccio Cristina, Pecoraro Giovanni, Molinaro Antonio, Smaldone Giovanni, Kim Jeon-Kyung, Kim Dong-Hyun, Paduano Luigi, Di Lorenzo Flaviana, Silipo Alba

机构信息

Department of Chemical Sciences and Task Force for Microbiome Studies, University of Naples Federico II, Via Cinthia 4, 80126 Naples, Italy.

CSGI, Center for Colloid and Surface Science, Sesto Fiorentino, Florence 50019, Italy.

出版信息

JACS Au. 2025 Jun 24;5(7):3311-3327. doi: 10.1021/jacsau.5c00441. eCollection 2025 Jul 28.

Abstract

Gram-negative bacterium , which is increasingly prevalent in elderly individuals, is associated with cognitive decline and gut-brain axis dysfunction. Here, we present a comprehensive structural characterization of lipopolysaccharide (LPS), a key modulator of immune recognition and the main component of its outer membrane. Using a multidisciplinary approach combining chemical, spectroscopic, spectrometric, biophysical and computational methods, we unveil a unique O-antigen characterized by a trisaccharide repeating unit containing rhamnose and glucosamine, displaying nonstoichiometric O-acetylation and a terminal methylated rhamnose capping the saccharide chain. Furthermore, we disclose a short core oligosaccharide and a Lipid A composed of penta- to tetra-acylated species. Notably, this LPS exhibits reduced activation of Toll-Like Receptor-dependent signaling compared to the highly immunostimulatory LPS and elicits a poor pro-inflammatory cytokine response. Moreover, LPS exhibits selective binding to immune lectins such as Ficolin-3 and Galectin-4, as shown by the microarray assays. This raises the possibility that lectin-mediated recognition may represent an alternative route of immune engagement, which could help explain altered immune responses observed in elderly individuals. These findings provide a molecular basis for further exploring the role of LPS in microbiota-induced immune modulation and its possible impact on age-related inflammatory and neurodegenerative conditions.

摘要

革兰氏阴性菌在老年人中越来越普遍,与认知能力下降和肠脑轴功能障碍有关。在这里,我们展示了脂多糖(LPS)的全面结构特征,脂多糖是免疫识别的关键调节因子,也是其外膜的主要成分。我们采用化学、光谱、质谱、生物物理和计算方法相结合的多学科方法,揭示了一种独特的O抗原,其特征是含有鼠李糖和葡糖胺的三糖重复单元,表现出非化学计量的O-乙酰化,并且糖链末端有一个甲基化的鼠李糖封端。此外,我们还揭示了一个短的核心寡糖和一个由五酰化到四酰化物种组成的脂质A。值得注意的是,与高度免疫刺激的LPS相比,这种LPS对Toll样受体依赖性信号传导的激活作用降低,并且引发较弱的促炎细胞因子反应。此外,如微阵列分析所示,LPS对免疫凝集素如ficolin-3和galectin-4表现出选择性结合。这增加了凝集素介导的识别可能代表免疫参与的另一种途径的可能性,这有助于解释在老年人中观察到的免疫反应改变。这些发现为进一步探索LPS在微生物群诱导的免疫调节中的作用及其对与年龄相关的炎症和神经退行性疾病的可能影响提供了分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb8/12308378/b86e9089d5fa/au5c00441_0001.jpg

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