Novel insights into the immune regulatory effects of Megalobrama amblycephala intelectin on the phagocytosis and killing activity of macrophages. (September 2021)

• Record Type: Journal Article
• Authors: Zheng, Yancui; Liu, Yunlong; Li, Hongping; Wang, Xu; Zhang, Minying; Shen, Xin; Cheng, Hanliang; Xu, Jianhe; Wang, Xingqiang; Liu, Hong; Ding, Zhujin; Zhao, Xiaoheng
• Is Part Of: Molecular immunology. Volume 137(2021)
• Page Start: 145
• Page End: 154
• Publication Date: 2021-09
• Subjects: Megalobrama amblycephala -- Intelectin -- Digital Gene Expression Profiling -- Immune Regulatory Effects -- Signaling Pathways; Immunochemistry -- Periodicals; Molecular biology -- Periodicals; Immunochemistry -- Periodicals; Allergy and Immunology -- Periodicals; Molecular Biology -- Periodicals; Immunochimie -- Périodiques; Biologie moléculaire -- Périodiques; Immunochemistry; Molecular biology; Periodicals; Electronic journals; 571.96
• DOI: 10.1016/j.molimm.2021.06.008
• Languages: English
• ISSNs: 0161-5890

Abstract

Highlights: 1247 DEGs were identified by Digital Gene Expression Profiling, which should contribute to explore the regulation of MaINTL to macrophages. Plenty of DEGs were enriched in GO functional categories related to the phagocytosis and killing activity of macrophages. KEGG analysis revealed that many immune related pathways were activated. Numerous pro-inflammatory cytokines were induced upon rMaINTL treatment via signaling factors of MAPK signaling pathway. Abstract: Previous studies have found that the expression level of Megalobrama amblycephala intelectin (MaINTL) increased significantly post Aeromonas hydrophila infection, and recombinant MaINTL (rMaINTL) protein could activate macrophages and enhance the phagocytosis and killing activity of macrophages. In order to reveal the immune regulatory mechanisms of MaINTL, primary M. amblycephala macrophages were treated with endotoxin-removed rMaINTL and GST-tag proteins, then total RNA were extracted and used for comparative Digital Gene Expression Profiling (DGE). 1247 differentially expressed genes were identified by comparing rMaINTL and GST-tag treated macrophage groups, including 482 up-regulated unigenes and 765 down-regulated unigenes. In addition, eleven randomly selected differentially expressed genes were verified by qRT-PCR, and most of them shared the similar expression patterns as that of DGE results. GO enrichment revealed that the differentially expressed genes were mainly concentrated in the membrane part and cytoskeleton of cellular component, the binding and signal transducer activity of molecular function, the cellular process, regulation of biological process, signaling and localization of biological process, most of which might related with the phagocytosis and killing activity of macrophages. KEGG analysis revealed the activation and involvement of differentially expressed genes in immune related pathways, such as Tumor necrosis factor (TNF) signaling pathway, Interleukin 17 (IL-17) signaling pathway, Toll-like receptor signaling pathway, and NOD like receptor signaling pathway, etc. In these pathways, TNF-ɑ, Activator protein-1 (AP-1), Myeloid differentiation primary response protein MyD88 (MyD88), NF-kappa-B inhibitor alpha (ikBɑ) and other key signaling factors were significantly up-regulated. These results will be helpful to clarify the immune regulatory mechanisms of fish intelectin on macrophages, thus providing a theoretical basis for the prevention and control of fish bacterial diseases.