Cong Bailin, Han Guang, Huang Xiao-Hang, Liu Sheng-Hao, Liu Chen-Lin, Lin Xue-Zheng, He Pei-Qing, Gasaino Herbert
The Key Laboratory of Marine Bioactive Substance, SOA, Qingdao 266061, PR China.
Fish Shellfish Immunol. 2009 Aug;27(2):221-9. doi: 10.1016/j.fsi.2009.05.008. Epub 2009 May 28.
Calcium-activated potassium channels on plasma membrane enable potassium influx into the cell with ensuing changes in plasma membrane potential and consequent effects on cellular metabolic functions. Recently, this potassium channel was reported to regulate the cellular responses of mammalian immune cells. We have postulated the presence of such a channel in fish immune cells and its potential role in immunoregulation in fish. Employing specific primers and RNA template, we cloned a segment of a novel gene from turbot blood sample and subsequently obtained a full cDNA sequence using RACE approaches. Bioinformatic analysis revealed structural and phylogenetic characteristics of a novel small conductance calcium-activated potassium channel gene, we called TSKCa, which exhibits homologous domains to other species particularly in the transmembrane regions. Full-length TSKCa cDNA is 1698 bp with a 1632 bp open reading frame encoding a protein of 544 amino acids. TSKCa gene is expressed in majority of the tested organs and tissues of turbot. To assess the postulated immune function of TSKCa, we infected turbot with the pathogen Vibrio anguillarum. Here, semi-quantitative RT-PCR analysis demonstrated increased mRNA expression of TSKCa in head kidney, spleen and blood, indicating an important role of TSKCa in these organ tissues that mediate the immune defense response of turbot. In contrast, there was less change in expression in the turbot intestines and liver which were less implicated in the immune response in present study.
质膜上的钙激活钾通道使钾离子流入细胞,随之质膜电位发生变化,进而影响细胞代谢功能。最近,据报道这种钾通道可调节哺乳动物免疫细胞的细胞反应。我们推测鱼类免疫细胞中存在这样一种通道,并且它在鱼类免疫调节中具有潜在作用。利用特异性引物和RNA模板,我们从大菱鲆血液样本中克隆了一个新基因的片段,随后采用RACE方法获得了完整的cDNA序列。生物信息学分析揭示了一种新的小电导钙激活钾通道基因的结构和系统发育特征,我们将其命名为TSKCa,它在跨膜区域与其他物种具有同源结构域。TSKCa cDNA全长1698 bp,开放阅读框为1632 bp,编码一个544个氨基酸的蛋白质。TSKCa基因在大菱鲆大多数被检测的器官和组织中均有表达。为了评估TSKCa假定的免疫功能,我们用病原菌鳗弧菌感染大菱鲆。在此,半定量RT-PCR分析表明,TSKCa在头肾、脾脏和血液中的mRNA表达增加,表明TSKCa在这些介导大菱鲆免疫防御反应的器官组织中具有重要作用。相比之下,在本研究中较少参与免疫反应的大菱鲆肠道和肝脏中的表达变化较小。