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白术多糖激活脾细胞信号通路研究

Signaling pathway underlying splenocytes activation by polysaccharides from Atractylodis macrocephalae Koidz.

机构信息

Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou 310058, PR China.

出版信息

Mol Immunol. 2019 Jul;111:19-26. doi: 10.1016/j.molimm.2019.03.004. Epub 2019 Apr 3.

Abstract

Previous study demonstrated that total polysaccharides isolated from Atractylodis macrocephalae Koidz. (RAMPtp) were effective to eliminate intramammary infection in cows. The present study was designed to investigate the immunomodulatory activity of RAMPtp in mouse splenocytes. Splenocyte proliferation, natural killer (NK) cytotoxicity, productions of NO and cytokines, transcription factor activity as well as the signal pathways and receptor were examined. The results showed that RAMPtp significantly promoted splenocyte proliferation and made the cells enter S and G2/M phases, increased ratios of T/B cells, boosted NK cytotoxicity, enhanced transcriptional activities of nuclear factor of activated T cells (NFAT), nuclear factor κB (NF-κB) and activator protein 1 (AP-1), and stimulated secretions of NO, immunoglobulin G (IgG) and multiple cytokine families (IL-1α, IL-1β, IL-2, IL-3, IL-4, IL-6, IL-10, IL-12p40, IL-12p70, IL-13, IFN-γ, TNF-α, G-CSF, GM-CSF, KC, MIP-1α, MIP-1β, RANTES and Eotaxin). In addition, all the specific inhibitors against the mitogen-activated protein kinases (MAPKs) and NF-κB significantly suppressed the IL-6 production induced by RAMPtp. Moreover, splenocytes from Toll-like receptor 4 (TLR4) deficient mouse responded equally to RAMPtp stimulation as the wild-type. Therefore, RAMPtp might induce splenocytes activation at least in part via the TLR4-independent MAPKs and NF-κB signaling pathways. The present results would be useful to further understand the immunomodulatory mechanisms of RAMPtp in elimination of intramammary infection in cows.

摘要

先前的研究表明,从白术(Atractylodis macrocephalae Koidz.)中分离得到的总多糖(RAMPtp)可有效消除奶牛的乳腺炎感染。本研究旨在探讨 RAMPtp 对小鼠脾细胞的免疫调节活性。检测了脾细胞增殖、自然杀伤(NK)细胞毒性、NO 和细胞因子的产生、转录因子活性以及信号通路和受体。结果表明,RAMPtp 显著促进脾细胞增殖,使细胞进入 S 和 G2/M 期,增加 T/B 细胞比例,增强 NK 细胞毒性,增强核因子活化 T 细胞(NFAT)、核因子κB(NF-κB)和激活蛋白 1(AP-1)的转录活性,并刺激 NO、免疫球蛋白 G(IgG)和多种细胞因子家族(IL-1α、IL-1β、IL-2、IL-3、IL-4、IL-6、IL-10、IL-12p40、IL-12p70、IL-13、IFN-γ、TNF-α、G-CSF、GM-CSF、KC、MIP-1α、MIP-1β、RANTES 和 Eotaxin)的分泌。此外,所有针对丝裂原活化蛋白激酶(MAPKs)和 NF-κB 的特异性抑制剂均显著抑制了 RAMPtp 诱导的 IL-6 产生。此外,TLR4 缺陷型小鼠的脾细胞对 RAMPtp 刺激的反应与野生型相同。因此,RAMPtp 可能至少部分通过 TLR4 非依赖性 MAPKs 和 NF-κB 信号通路诱导脾细胞活化。本研究结果将有助于进一步了解 RAMPtp 在消除奶牛乳腺炎感染中的免疫调节机制。

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