MiR-155靶向talin-1基因调控柱状黄杆菌胞外多糖诱导的EPC细胞凋亡

MiR-155 regulates apoptosis induced by FC-EPS incubation via targeting the talin-1 gene in EPC

  • 摘要: 为研究 miR-155 在柱状黄杆菌胞外多糖 (FC-EPS) 诱导的细胞凋亡中的作用机制,本实验采用RNA干扰 (RNAi) 技术,通过过表达 miR-155 和敲降踝蛋白基因 (talin-1),皆能抑制 FC-EPS 诱导的细胞凋亡,并鉴定出 talin-1 为 miR-155 的靶蛋白。在 FC-EPS 诱导细胞凋亡的过程中,踝蛋白水平显著升高,在凋亡发生阶段检测到凋亡执行蛋白 Caspase-3 的活化,同时检测到2条踝蛋白剪切异构体,大小分别约为200 ku 和 250 ku;将构建的鲤 Talin-1 真核表达质粒转染鲤上皮瘤细胞 (EPC),过表达的 Talin-1 延迟且延长了细胞凋亡的进程,并检测到上述2条踝蛋白异构体。然而,当以 FC-EPS 转染 EPC 细胞时,Talin-1 先下降再恢复到正常水平,细胞不发生凋亡。因此,在 FC-EPS 诱导细胞凋亡的过程中,细胞通过上调 miR-155 来调控靶基因 talin-1 mRNA 和蛋白转录的变化,以及产生 Talin-1 蛋白异构体来抑制细胞发生凋亡。本研究为有效防治柱状黄杆菌疾病提供新思路。

     

    Abstract: Incubation of Flavobacterium columnare exopolysaccharide (FC-EPS) significantly increases the expression of miR-155 in epithelioma papulosum cyprinid (EPC) cell line, leading to cell apoptosis. In order to study the mechanism of miR-155 in FC-EPS induced apoptosis, RNAi technology was used in this research. It was found that both overexpression of miR-155 and talin-1 knockout could inhibit apoptosis induced by FC-EPS incubation. Then, talin-1 was identified as the target protein of miR-155 by EMSA assay. During the process of apoptosis induced by FC-EPS incubation, the Talin-1 protein was significantly increased, and the activation of apoptosis executioner caspase-3 protein was detected. At the same time, two talin-1 isomers (about 200 ku and 250 ku, respectively) were obtained. Subsequently, the talin-1 gene inserted in plasmid pcDNA3.1 was constructed and transfected into EPC cells, the overexpressed Talin-1 protein delayed and prolonged the process of apoptosis, and two Talin-1 isomers mentioned above were detected. However, apoptosis did not occur when EPC cells were transfected with FC-EPS; on this occasion, the Talin-1 protein in EPC went down at first, then returned to normal level. Hence, in the context of apoptosis induced by FC-EPS incubation, EPC cells reduces apoptosis by regulating the level of mRNA and protein transcription of talin-1 through up-regulation of miR-155 and producing Talin-1 isomers. This paper provides a new idea for effective prevention and treatment of F. columnare diseases.

     

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