Wei Jing, Yu Lintian, Sun Lina, Zhang Xiaoping, Li Minghui, Qi Wenchuang, Zhou Linyan, Wang Deshou
Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), School of Life Science, Southwest University, Chongqing 400715, China.
Vet Immunol Immunopathol. 2013 Sep 1;155(1-2):48-56. doi: 10.1016/j.vetimm.2013.06.004. Epub 2013 Jun 7.
Foxp3 is a crucial transcription factor for the development and function of CD4(+)CD25(+) regulatory T cells (Tr) which play a key role in preventing autoimmune diseases and maintaining maternal-fetal tolerance in mammals. However, the knowledge of Foxp3 and its regulation in teleosts is limited. In the present study, the Foxp3 cDNA was cloned from Nile tilapia and characterized. The full length cDNA of Nile tilapia (nt)Foxp3 contained a 5'UTR of 104 bp, a 3'UTR of 239 bp and an open reading frame of 1134 bp. The putative ntFoxp3 contained a C2H2 zinc finger domain, a winged-helix/fork head domain and a leucine zipper-like domain with a consensus of V-x(6)-L-x(6)-L-x(6)-L, which are typical motifs of a Foxp3. The highest mRNA expression of ntFoxp3 was observed in the spleen, with moderate expression in the head kidney, intestine, kidney, liver and brain. Stimulation of peripheral blood mononuclear cells with PHA and LPS led to a significant increase of ntFoxp3 mRNA expression at 6 and 24h, respectively. In contrast, stimulation with PMA had no effect during the sampling period. After injecting 1×10(7) cells of live Aeromonas hydrophila into adult female Nile tilapias, the mRNA expression of ntFoxp3 significantly increased in the gill and intestine at 6h, while unchanged in the spleen. In all the tissues examined, a clearly up-regulation of ntFoxp3 expression was detected at 24h after the second challenge. These results suggest that ntFoxp3 might be involved into lymphocyte activation and immune responses as reported in mammals. Meanwhile, the correlation between the expression profile of ntFoxp3 and serum estrogen (17-beta-estradiol, E2) concentration was investigated by real-time PCR and enzyme immunoassay. The results showed that E2 could regulate the expression of ntFoxp3 in the intestine and kidney but not in the spleen. This work will help future investigations into Tr cells and extend our understanding of interactions between sex hormones and immune related molecules in teleosts.
Foxp3是CD4(+)CD25(+)调节性T细胞(Tr)发育和功能的关键转录因子,在预防自身免疫性疾病和维持哺乳动物母胎耐受中起关键作用。然而,硬骨鱼中Foxp3及其调控的相关知识有限。在本研究中,尼罗罗非鱼的Foxp3 cDNA被克隆并进行了特征分析。尼罗罗非鱼(nt)Foxp3的全长cDNA包含104 bp的5'UTR、239 bp的3'UTR和1134 bp的开放阅读框。推测的ntFoxp3包含一个C2H2锌指结构域、一个翼状螺旋/叉头结构域和一个具有V-x(6)-L-x(6)-L-x(6)-L一致序列的亮氨酸拉链样结构域,这些是Foxp3的典型基序。ntFoxp3的mRNA在脾脏中表达最高,在头肾、肠道、肾脏、肝脏和大脑中表达中等。用PHA和LPS刺激外周血单核细胞分别导致ntFoxp3 mRNA表达在6小时和24小时显著增加。相反,在采样期间用PMA刺激没有效果。将1×10(7)个嗜水气单胞菌活细胞注射到成年雌性尼罗罗非鱼体内后,ntFoxp3的mRNA在鳃和肠道中于6小时显著增加,而在脾脏中不变。在第二次攻击后24小时,在所有检测的组织中均检测到ntFoxp3表达明显上调。这些结果表明,ntFoxp3可能如在哺乳动物中报道的那样参与淋巴细胞活化和免疫反应。同时,通过实时PCR和酶免疫测定研究了ntFoxp3表达谱与血清雌激素(17-β-雌二醇,E2)浓度之间的相关性。结果表明,E2可调节ntFoxp3在肠道和肾脏中的表达,但不能调节在脾脏中的表达。这项工作将有助于未来对Tr细胞的研究,并扩展我们对硬骨鱼中性激素与免疫相关分子之间相互作用的理解。