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一种果聚糖型大蒜多糖可上调巨噬细胞和免疫抑制小鼠的免疫应答。

A fructan-type garlic polysaccharide upregulates immune responses in macrophage cells and in immunosuppressive mice.

机构信息

Department of Food Science and Engineering, Jinan University, Guangzhou 510632, China; Department of Mechanical Engineering, University of Canterbury, Private Bag 4800, 8140 Christchurch, New Zealand.

Department of Food Science and Engineering, Jinan University, Guangzhou 510632, China.

出版信息

Carbohydr Polym. 2024 Nov 15;344:122530. doi: 10.1016/j.carbpol.2024.122530. Epub 2024 Jul 25.

Abstract

The anti-inflammatory effects of plant polysaccharides are well known. However, the stimulatory effects of polysaccharides under immunosuppressive conditions and their link with the polysaccharide structure is underexplored. In this work, the immune modulatory effects of a garlic polysaccharide (GP) are investigated via in vitro and vivo methods. It is observed that GP enhance the immune response of macrophages (RAW264.7) as indicated by the elevated levels of nitric oxide, TNF-α and IL-6. The observation that GP are able to stimulate the immune response in vitro was then explored with the use of an immunosuppressed mouse model. Surprisingly, GP exhibited dose-dependent up-regulatory impacts on the cyclophosphamide (CTX) suppressed levels of cytokines such as IFN-γ and IL-6 and immunoglobulins (e.g. IgA and IgG). The GP intervention reversed histopathological damage to the small intestine and spleen and increased fecal short-chain fatty acid levels. Moreover, GP modulates the gut microbiota dysbiosis by increasing the abundance of immunogenic bacteria such as g__norank_f__Erysipelotrichaceae, while inhibiting the over-abundance of g_Bacteroides. Functional predictions indicated that gut biomarkers of GP possessed the functions of glycoside hydrolase family 32 (GH32) and β-fructofuranosidase. It is concluded that GP is a promising immunostimulant for immune-compromised individuals.

摘要

植物多糖的抗炎作用是众所周知的。然而,多糖在免疫抑制条件下的刺激作用及其与多糖结构的关系还没有得到充分的研究。在这项工作中,通过体外和体内方法研究了大蒜多糖 (GP) 的免疫调节作用。研究结果表明,GP 增强了巨噬细胞 (RAW264.7) 的免疫反应,表现为一氧化氮、TNF-α 和 IL-6 水平升高。然后,使用免疫抑制小鼠模型探索了 GP 在体外刺激免疫反应的能力。令人惊讶的是,GP 对环磷酰胺 (CTX) 抑制的细胞因子(如 IFN-γ 和 IL-6)和免疫球蛋白(如 IgA 和 IgG)水平表现出剂量依赖性的上调作用。GP 干预逆转了小肠和脾脏的组织病理学损伤,并增加了粪便短链脂肪酸水平。此外,GP 通过增加免疫原性细菌(如 g__norank_f__Erysipelotrichaceae)的丰度,同时抑制 g_Bacteroides 的过度丰度,调节肠道微生物群失调。功能预测表明,GP 的肠道生物标志物具有糖苷水解酶家族 32 (GH32) 和 β-呋喃果糖苷酶的功能。研究结果表明,GP 是一种有前途的免疫刺激剂,可用于免疫功能低下的个体。

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