Literature DB >> 21167199

A primitive Toll-like receptor signaling pathway in mollusk Zhikong scallop Chlamys farreri.

Mengqiang Wang1, Jialong Yang, Zhi Zhou, Limei Qiu, Lingling Wang, Huan Zhang, Yang Gao, Xingqiang Wang, Li Zhang, Jianmin Zhao, Linsheng Song.   

Abstract

As a member of pattern-recognition receptors (PRRs), the Toll-like receptor (TLR) and its signaling pathway play pivotal roles in recognizing various pathogen-associated molecular patterns (PAMPs), and buildup the front-line against invading pathogens. In the present study, the sequence features and mRNA expression profiles of five key genes involved in TLR signal pathway were characterized, and their functions in the immune responses were also investigated in order to validate the TLR signaling pathway and its potential roles in the immune defense of Zhikong scallop Chlamys farreri. These five genes, including CfTLR, CfMyD88, CfTRAF6, CfIκB and CfNFκB, exhibited significant similarity with their homologues from other model organisms, and contained the typical motifs. A strong interaction between the TIR domain from CfTLR and CfMyD88 protein was revealed via ELISA assays. The mRNA transcripts of these five genes were all up-regulated after LPS stimulation, indicating that they were involved in the immune response against LPS. When CfTLR expression was inhibited by RNAi technology, the mRNA expression level of CfMyD88, CfTRAF6, CfIκB, CfNFκB and G-type lysozyme were all decreased, while those of superoxide dismutase and catalase were increased. After Listonella anguillara challenge, the apoptosis level of those CfTLR-suppressed scallops was significantly lower than that in control groups (p<0.05) at the beginning of bacteria challenge, while the cumulative mortality was significantly higher than that of control groups (p<0.05). These results collectively favored that a rather canonical MyD88-dependent TLR pathway existed in scallop and this pathway was involved in immune signaling to active the diverse downstream reaction including anti-oxidant, anti-bacteria and apoptosis.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21167199     DOI: 10.1016/j.dci.2010.12.005

Source DB:  PubMed          Journal:  Dev Comp Immunol        ISSN: 0145-305X            Impact factor:   3.636


  18 in total

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