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槟榔多糖通过NF-κB和MAPK途径诱导M1巨噬细胞极化,且不依赖于TLR2和TLR4信号传导。

Areca nut polysaccharide induces M1 macrophage polarization through the NF-κB and MAPK pathways independent of TLR2 and TLR4 signaling.

作者信息

Luo Qiyuan, Wang Quanjiang, Wu Haowen, Chen Yun

机构信息

Sanya Institute of Breeding and Multiplication, School of Tropical Agriculture and Forestry, Hainan University, Sanya 572025, PR China.

Sanya Institute of Breeding and Multiplication, School of Tropical Agriculture and Forestry, Hainan University, Sanya 572025, PR China.

出版信息

Int J Biol Macromol. 2024 Nov;281(Pt 3):136379. doi: 10.1016/j.ijbiomac.2024.136379. Epub 2024 Oct 11.

DOI:10.1016/j.ijbiomac.2024.136379
PMID:39396589
Abstract

In this study, the structure of Areca nut polysaccharide (ANP) was characterized, and its effects on macrophage activation and the underlying molecular mechanisms were investigated. ANP was identified as a glucan with a molecular weight of 24.5 kDa, and its structure was analyzed using XRD, SEM, FT-IR, methylation, and NMR techniques. The main chain of ANP is composed of →4)-α-D-Glcp-(1 → and →4,6)-α-D-Glcp-(1→, with a branched α-D-Glcp-(1 → chain. Furthermore, the activation of macrophages by ANP was explored. Stimulation of RAW264.7 cells with ANP in vitro increased the expression of inflammatory cytokines (TNF-α and IL-6) and NO levels. Flow cytometry showed that ANP induced M1 macrophage polarization. RNA-seq and Western blot analyses revealed that ANP activated the NF-κB and MAPK pathways. Importantly, TLR2- and TLR4- specific antibodies did not affect ANP-induced M1 polarization, whereas endocytosis inhibitors reduced the production of inflammatory cytokines in ANP-treated macrophages. In conclusion, ANP engages macrophages without interacting with TLR2 and TLR4 receptors, inducing M1 polarization through the NF-κB and MAPK signaling pathways.

摘要

在本研究中,对槟榔多糖(ANP)的结构进行了表征,并研究了其对巨噬细胞激活的影响及潜在分子机制。ANP被鉴定为一种分子量为24.5 kDa的葡聚糖,并使用X射线衍射(XRD)、扫描电子显微镜(SEM)、傅里叶变换红外光谱(FT-IR)、甲基化和核磁共振(NMR)技术对其结构进行了分析。ANP的主链由→4)-α-D-葡萄糖-(1→和→4,6)-α-D-葡萄糖-(1→组成,带有一个分支的α-D-葡萄糖-(1→链。此外,还探究了ANP对巨噬细胞的激活作用。体外使用ANP刺激RAW264.7细胞可增加炎性细胞因子(TNF-α和IL-6)的表达及一氧化氮(NO)水平。流式细胞术显示ANP诱导M1巨噬细胞极化。RNA测序(RNA-seq)和蛋白质免疫印迹分析表明ANP激活了核因子κB(NF-κB)和丝裂原活化蛋白激酶(MAPK)信号通路。重要的是,TLR2和TLR4特异性抗体不影响ANP诱导的M1极化,而内吞作用抑制剂可降低ANP处理的巨噬细胞中炎性细胞因子的产生。总之,ANP与巨噬细胞结合但不与TLR2和TLR4受体相互作用,通过NF-κB和MAPK信号通路诱导M1极化。

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