Xie Xiao-Dong, Tang Min, Yi Shou-Li, He Ying, Chen Si-Yu, Zhao Yi, Chen Qi, Cao Mi-Xia, Yu Mei-Ling, Wei Ying-Yi, Yu Wei-Hua, Hu Ting-Jun
College of Animal Science and Technology, Guangxi University, Nanning 530005, China.
Department of Clinical Laboratory, Xinqiao Hospital, Army Medical University, Chongqing 400037, China.
Phytomedicine. 2024 Feb;124:155294. doi: 10.1016/j.phymed.2023.155294. Epub 2023 Dec 17.
Innate immune memory of macrophages is closely linked to histone modifications. While various studies have demonstrated that the polysaccharide of Asparagus cochinchinensis (Lour.) Merr (ACMP), extracted through alcohol-alkali extraction, enhances macrophages' non-specific immune function; no literature currently addresses whether ACMP's regulatory effect is related to innate immune memory and histone modification.
This study aims to investigate if ACMP induces innate immune memory emergence in macrophages via pattern recognition receptor (PRR).
After co-incubating different doses of ACMP with RAW264.7 cells and BMDM cells, we observed changes in signaling pathways related to PRR and assessed the presence of innate immune memory phenomenon in the cells.
We observed the morphological characteristics of the ACMP using a scanning electron microscope, infrared spectrum, and HPLC pre-column derivatization method. We used q-PCR, Western blot, RNA-seq, and CUT&Tag-seq methods to examine ACMP's regulation of macrophage immune response and innate immune memory and explored its specific mechanism.
ACMP, primarily composed of Man, GlcN, Rha, Fuc, GalA, Xyl, Glc, Gal, Ara, and, exhibited a molar ratio of each monosaccharide (1.41: 0.35: 0.49: 0.18: 1.00: 97.12: 0.36: 3.58: 1.14). ACMP regulated immunological function in macrophages through the TLR4-MAPK-JNK/p38/ERK pathway. ACMP induced elevated levels of chromosomal H3K4me1, enhancing TNF-α, IL-1β, and other genes' responsiveness, allowing macrophages to develop innate immune memory to ACMP stimulation.
This study first time demonstrates that ACMP regulates immunological function through the TLR4-MAPK-JNK/ERK/p38 signaling pathway, distinct from prior reports. ACMP induces innate immune memory in macrophages in response to its immune stimulation by promoting increased H3K4me1 on chromosomes. This mechanism may be crucial in how plant polysaccharides regulate macrophages and the body's immune function.
巨噬细胞的固有免疫记忆与组蛋白修饰密切相关。虽然各种研究表明,通过醇碱提取法提取的天门冬多糖(ACMP)可增强巨噬细胞的非特异性免疫功能;但目前尚无文献探讨ACMP的调节作用是否与固有免疫记忆和组蛋白修饰有关。
本研究旨在探讨ACMP是否通过模式识别受体(PRR)诱导巨噬细胞产生固有免疫记忆。
将不同剂量的ACMP与RAW264.7细胞和骨髓来源的巨噬细胞(BMDM)共同孵育后,观察与PRR相关的信号通路变化,并评估细胞中固有免疫记忆现象的存在情况。
我们使用扫描电子显微镜、红外光谱和HPLC柱前衍生化方法观察ACMP的形态特征。我们使用q-PCR、蛋白质免疫印迹法、RNA测序和CUT&Tag测序方法来检测ACMP对巨噬细胞免疫反应和固有免疫记忆的调节作用,并探索其具体机制。
ACMP主要由甘露糖(Man)、氨基葡萄糖(GlcN)、鼠李糖(Rha)、岩藻糖(Fuc)、半乳糖醛酸(GalA)、木糖(Xyl)、葡萄糖(Glc)、半乳糖(Gal)、阿拉伯糖(Ara)组成,各单糖的摩尔比为(1.41: 0.35: 0.49: 0.18: 1.00: 97.12: 0.36: 3.58: 1.14)。ACMP通过TLR4-MAPK-JNK/p38/ERK途径调节巨噬细胞的免疫功能。ACMP诱导染色体H3K4me1水平升高,增强肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)等基因的反应性,使巨噬细胞对ACMP刺激产生固有免疫记忆。
本研究首次证明ACMP通过TLR4-MAPK-JNK/ERK/p38信号通路调节免疫功能,这与先前的报道不同。ACMP通过促进染色体上H3K4me1增加,诱导巨噬细胞对其免疫刺激产生固有免疫记忆。该机制可能对植物多糖调节巨噬细胞和机体免疫功能具有重要意义。