TY - JOUR
T1 - A primitive Toll-like receptor signaling pathway in mollusk Zhikong scallop Chlamys farreri
AU - Wang, Mengqiang
AU - Yang, Jialong
AU - Zhou, Zhi
AU - Ziu, Limei
AU - Wang, Lingling
AU - Zhang, Huan
AU - Gao, Yang
AU - Wang, Xingqiang
AU - Zhang, Li
AU - Zhao, Jianmin
AU - Song, Linsheng
PY - 2011/4
Y1 - 2011/4
N2 - 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.
AB - 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.
KW - Chlamys farreri
KW - Innate immunity
KW - TLR signaling pathway\
UR - https://www.scopus.com/pages/publications/79952009250
U2 - 10.1016/j.dci.2010.12.005
DO - 10.1016/j.dci.2010.12.005
M3 - 文章
C2 - 21167199
AN - SCOPUS:79952009250
SN - 0145-305X
VL - 35
SP - 511
EP - 520
JO - Developmental and Comparative Immunology
JF - Developmental and Comparative Immunology
IS - 4
ER -