MAp34 Regulates the Non-specific Cell Immunity of Monocytes/Macrophages and Inhibits the Lectin Pathway of Complement Activation in a Teleost Fish

被引:20
作者
Mu, Liangliang [1 ]
Yin, Xiaoxue [1 ]
Wu, Hairong [1 ]
Han, Kailiang [1 ]
Guo, Zheng [1 ]
Ye, Jianmin [1 ]
机构
[1] South China Normal Univ, Inst Modern Aquaculture Sci & Engn, Sch Life Sci, Guangdong Prov Key Lab Hlth & Safe Aquaculture, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Oreochromis niloticus; MAp34; non-specific cell immunity; competitive inhibition; lectin pathway; MANNAN-BINDING LECTIN; PATTERN-RECOGNITION MOLECULES; TILAPIA OREOCHROMIS-NILOTICUS; SERINE PROTEASES MASPS; FUNCTIONAL-CHARACTERIZATION; IN-VITRO; INNATE; IDENTIFICATION; EXPRESSION; PROTEIN;
D O I
10.3389/fimmu.2020.01706
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The lectin pathway of the complement system is one of the main components of innate immunity, which plays a pivotal role in the defense against infectious microorganisms and maintains immune homeostasis. However, its control mechanisms remain unclear in teleost fish. In this study, we described the identification and functional characterization of a mannose-binding lectin associated protein MAp34 (OnMAp34) from Nile tilapia (Oreochromis niloticus) at molecular, cellular, and protein levels. The open reading frame (ORF) ofOnMAp34is 918 bp of nucleotide sequence encoding a polypeptide of 305 amino acids. The deduced amino acid sequence has three characteristic structures, including two C1r/C1s-Uegf-BMP domains (CUB) and one epidermal growth factor domain (EGF). Expression analysis revealed that theOnMAp34was highly expressed in the liver and widely existed in other examined tissues. In addition, the mRNA and protein expression levels of OnMAp34 were remarkably altered upon infection withStreptococcus agalactiaeandAeromonas hydrophila in vivoandin vitro. Further, we found that the OnMAp34 could participate in the non-specific cellular immune defense, including the regulation of inflammation, migration, and enhancement of phagocytosis of monocytes/macrophages. Moreover, the OnMAp34 could compete with OnMASPs to combine OnMBL and inhibit the lectin pathway of complement activation. Overall, our results provide new insights into the understanding of MAp34 as a potent regulator in the lectin complement pathway and non-specific cell immunity in an early vertebrate.
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页数:14
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