4.7 Article

Polyethylenimine-coated PLGA nanoparticles containing Angelica sinensis polysaccharide promote dendritic cells activation and associated molecular mechanisms

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 207, Issue -, Pages 559-569

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2022.03.038

Keywords

Angelica sinensis polysaccharide; Cationic PLGA nanoparticles; Dendritic cells; RNA-seq; Molecular mechanisms

Funding

  1. National Natural Science Foun-dation of China [32072905, 31872509]
  2. Fundamental Research Funds for the Central Universities [KYZ201844]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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In this study, the effects of polyethylenimine-coated PLGA nanoparticles containing Angelica sinensis polysaccharide (ASP) on dendritic cells (DCs) activation and maturation were investigated. RNA-seq analysis revealed differentially expressed genes between ASP-PLGA-PEI and control group, and KEGG pathway analysis showed the involvement of various pathways in DCs activation. Furthermore, the JAK2/STAT3 signaling pathway was found to play a crucial role in the DCs activation and maturation induced by ASP-PLGA-PEI nanoparticles.
Cationic PLGA nanoparticles-based delivery systems have been extensively employed as nanocarriers for drugs and antigens in recent years. Herein, we investigated the effects of polyethylenimine-coated PLGA nanoparticles containing Angelica sinensis polysaccharide (ASP) system (ASP-PLGA-PEI) on dendritic cells (DCs) activation and maturation, and further explored the changes of transcriptome and underlying mechanism of DCs activation based on RNA-seq. Our results demonstrated that ASP-PLGA-PEI obviously promoted the activation and maturation of DCs. Meanwhile, RNA-seq analysis results exhibited 2812 differentially expressed genes (DEGs) between ASP-PLGA-PEI and control group, and the DCs activation by ASP-PLGA-PEI stimulation mainly related to phagosome, antigen processing and presentation, proteasome, lysosome, protein processing in endoplasmic reticulum and other pathways by KEGG pathways analysis. Furthermore, ASP-PLGA-PEI nanoparticles increased the levels of pJAK2 protein, and the expression of co-stimulatory molecules and cytokines induced by ASP-PLGAPEI nanoparticles were decreased with the presence of the inhibitor of JAK2/STAT3 signaling pathway. In addition, the nanoparticles were internalized by DCs mainly through the clathrin-mediated endocytosis and micropinocytosis. These results suggested that the DCs activation and maturation stimulated by ASP-PLGA-PEI were regulated via a complex interaction network, in which the JAK2/STAT3 signaling pathway played a crucial role.

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