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地黄多糖作为黏膜佐剂在诱导纵隔淋巴结树突状细胞活化中的作用。

Rehmannia glutinosa polysaccharide functions as a mucosal adjuvant to induce dendritic cell activation in mediastinal lymph node.

机构信息

Department of Chemistry, Pukyong National University, Busan 48513, South Korea; Marine-Integrated Bionics Research Center, Pukyong National University, Busan 48513, South Korea.

College of Electrical and Computer Engineering, Chungbuk National University, Cheongju 28644, South Korea.

出版信息

Int J Biol Macromol. 2018 Dec;120(Pt B):1618-1623. doi: 10.1016/j.ijbiomac.2018.09.187. Epub 2018 Sep 30.

Abstract

In our previous study, we showed that Rehmannia glutinosa polysaccharide (RGP) treatment induced activation of dendritic cells (DCs) in human and mouse subjects. In this study, we evaluated the effect of RGP as a mucosal adjuvant for inducting activation of DCs in the mediastinal lymph node (mLN) in the mouse. The C57BL/6 mice were intranasally (i.n.) treated with RGP and activation of DC in the mLN was analyzed. The treatment with RGP induced a substantial increase in the number of DCs in the mLN due to the up-regulation of C-C motif chemokine receptor 7 (CCR7) in the DCs. Moreover, the expression of co-stimulatory molecules in the mLN DCs and the concentration of pro-inflammatory cytokines in the lung were up-regulated by RGP treatment. Also, RGP treatment induced interferon-gamma (IFN-γ) and tumor necrosis factor-alpha (TNF-α) production in the mLN T cells. The combination treatment of RGP and ovalbumin (OVA) induced OVA-specific TCR transgenic I (OT-I) and OT-II cell proliferation in the mLN. Finally, the combination treatment of RGP and tyrosinase-related protein 2 (TRP2) peptide, a melanoma self-antigen, protected mice from melanoma challenge. Thus, these data demonstrated that RGP can be used as a mucosal adjuvant for inducing activation of immune responses in the lung.

摘要

在我们之前的研究中,我们表明地黄多糖(RGP)处理诱导人源和鼠源树突状细胞(DC)的活化。在本研究中,我们评估了 RGP 作为黏膜佐剂在诱导小鼠纵隔淋巴结(mLN)中 DC 活化的作用。用 RGP 经鼻腔(i.n.)处理 C57BL/6 小鼠,并分析 mLN 中 DC 的活化。由于 DC 中 C 型趋化因子受体 7(CCR7)的上调,RGP 处理导致 mLN 中 DC 的数量显著增加。此外,mLN DC 中共刺激分子的表达和肺中促炎细胞因子的浓度也因 RGP 处理而上调。而且,RGP 处理诱导 mLN T 细胞产生干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)。RGP 和卵清蛋白(OVA)的联合处理诱导 mLN 中的 OVA 特异性 TCR 转基因 I(OT-I)和 OT-II 细胞增殖。最后,RGP 和黑色素瘤自身抗原酪氨酸酶相关蛋白 2(TRP2)肽的联合处理可保护小鼠免受黑色素瘤的挑战。因此,这些数据表明 RGP 可作为诱导肺部免疫反应活化的黏膜佐剂。

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