Wei You Chuan, Pan Ting Shuang, Chang Ming Xian, Huang Bei, Xu Zhen, Luo Ting Rong, Nie P
Guangxi Key Laboratory of Subtropical Bioresource Conservation and Utilization, Guangxi University, 100 Daxue Road, Nanning, Guangxi Autonomous Region 530004, China.
Vet Immunol Immunopathol. 2011 Jun 15;141(3-4):173-82. doi: 10.1016/j.vetimm.2011.02.016. Epub 2011 Mar 2.
The two Toll-like receptors, TLR1 and TLR2 were cloned from orange-spotted grouper, Epinephelus coioides, an important teleost fish in mariculture of Asia. The cDNA sequences of TLR1 and TLR2 are 3195 and 3439 bp long, with an open reading frame (ORF) of 2406 and 2466 bp, encoding 801 and 821 amino acids, respectively. The TLR family motifs, i.e. leucine-rich repeat (LRR) domains and Toll/interleukin (IL)-1 receptor (TIR) domains are conserved in the TLR1 and TLR2, with nine and ten leucine-rich repeat (LRR) domains, and with one TIR domain, respectively. The TLR1 and TLR2 had a constitutive expression in examined organs/tissues of naïve orange-spotted grouper, and an increased expression of TLR1 and TLR2 at mRNA level was observed in immune organs such as in spleen of LPS and Poly(I:C) stimulated fish. An increased expression of TLR1 and TLR2 was also recorded in immune organs of the fish injected with the bacterial pathogen, Vibrio alginolyticus. Similarly, a significant rise in the expression of MyD88, an adaptor molecule which forms signalling complex with intracellular TIR domain, thus leading to the production of pro-inflammatory cytokines, such as IL-1β, was also observed in the LPS- and Poly(I:C)-stimulated, and V. alginolyticus-infected fish, indicating the possible role of TLR1 and TLR2 in the MyD88 signalling pathway. However, the mechanism involved in the increased expression of TLR1 and TLR2 following LPS and Poly(I:C) stimulation is at present unknown in fish, and further research should be carried out to identify ligands of fish TLR1 and TLR2 in order to understand the function of these receptors.
两种Toll样受体,即TLR1和TLR2,是从斜带石斑鱼(Epinephelus coioides)中克隆出来的,斜带石斑鱼是亚洲海水养殖中一种重要的硬骨鱼。TLR1和TLR2的cDNA序列分别长3195和3439 bp,开放阅读框(ORF)分别为2406和2466 bp,分别编码801和821个氨基酸。TLR家族基序,即富含亮氨酸重复序列(LRR)结构域和Toll/白细胞介素(IL)-1受体(TIR)结构域,在TLR1和TLR2中是保守的,分别有九个和十个富含亮氨酸重复序列(LRR)结构域,以及一个TIR结构域。TLR1和TLR2在未感染的斜带石斑鱼的检测器官/组织中组成性表达,在LPS和聚肌胞苷酸(Poly(I:C))刺激的鱼的脾脏等免疫器官中,观察到TLR1和TLR2在mRNA水平上表达增加。在用溶藻弧菌(Vibrio alginolyticus)这种细菌病原体注射的鱼的免疫器官中,也记录到TLR1和TLR2表达增加。同样,在LPS和聚肌胞苷酸(Poly(I:C))刺激以及溶藻弧菌感染的鱼中,也观察到髓样分化因子88(MyD88)表达显著升高,MyD88是一种衔接分子,与细胞内TIR结构域形成信号复合物,从而导致促炎细胞因子如IL-1β的产生,这表明TLR1和TLR2在MyD88信号通路中可能发挥作用。然而,目前鱼类中LPS和聚肌胞苷酸(Poly(I:C))刺激后TLR1和TLR2表达增加所涉及的机制尚不清楚,应该进行进一步研究以鉴定鱼类TLR1和TLR2的配体,以便了解这些受体的功能。