Duan Dianning, Shen Huawei, Pan Yanmin, Feng Rui, Zhang Lin, Lu Lingguang, Liu Jiankui, Qiu Longxin, Chen Hongbo
College of Life Science, Longyan University, Longyan 364012, Fujian, China.
Key Laboratory of Preventive Veterinary Medicine and Biotechnology (Longyan University), Longyan 364012, Fujian, China.
Sheng Wu Gong Cheng Xue Bao. 2022 Aug 25;38(8):2891-2901. doi: 10.13345/j.cjb.220239.
In order to investigate the apoptosis triggered by porcine circovirus type 2 (PCV2) in lymphocytes and the underlying mechanism, the levels of apoptosis and the expression levels of miRNA were examined by flow cytometry, Western blotting and real-time PCR (qPCR). The mimics or inhibitors of miR-125a-5p, an apoptosis-related miRNA, were transfected into PK-15 cells, and the apoptosis rate was examined upon overexpression or inhibition of mir-125a-5p. The target gene of mir-125a-5p was predicted by bioinformatics method, and the regulation of mir-125a-5p on the target gene was analyzed by luciferase reporter assay. The expressions of Bcl-2, Bax, cytochrome C and caspase-3 were detected by Western blotting. The results showed that exosomes secreted by PK-15 cells infected with PCV2 significantly increased the lymphocyte apoptosis rate, which was dose-dependent in certain concentration range. The expression of miR-125a-5p was dramatically increased. The apoptosis rate was increased significantly in the cells transfected with miR-125a-5p. It was predicted that there were binding sites of miR-125a-5p at 3'UTR by TargetScan. The luciferase activity of wild-type pmir-Bcl-2 3'UTR was inhibited significantly by miR-125a-5p mimics, but that of mutant pmir-Bcl-2 3'UTR was not changed. By Western blotting, Bcl-2 was reduced significantly, while Bax, cytochrome C and caspase-3 increased significantly, and the ratio of Bcl-2/Bax was significantly decreased. These results showed that PCV2 up-regulated the expression of miR-125a-5p through exosomes, then inhibited the expression of Bcl-2 at both mRNA and protein level, activated mitochondrial apoptosis pathway and induced apoptosis in lymphocytes.
为了研究猪圆环病毒2型(PCV2)在淋巴细胞中引发的凋亡及其潜在机制,通过流式细胞术、蛋白质免疫印迹法和实时荧光定量聚合酶链反应(qPCR)检测了凋亡水平和微小RNA(miRNA)的表达水平。将凋亡相关miRNA miR-125a-5p的模拟物或抑制剂转染到PK-15细胞中,在miR-125a-5p过表达或抑制后检测凋亡率。通过生物信息学方法预测miR-125a-5p的靶基因,并通过荧光素酶报告基因检测分析miR-125a-5p对靶基因的调控。通过蛋白质免疫印迹法检测Bcl-2、Bax、细胞色素C和半胱天冬酶-3的表达。结果表明,感染PCV2的PK-15细胞分泌的外泌体显著提高了淋巴细胞凋亡率,在一定浓度范围内呈剂量依赖性。miR-125a-5p的表达显著增加。转染miR-125a-5p的细胞凋亡率显著升高。通过TargetScan预测在3'非翻译区(UTR)存在miR-125a-5p的结合位点。miR-125a-5p模拟物显著抑制野生型pmir-Bcl-2 3'UTR的荧光素酶活性,但突变型pmir-Bcl-2 3'UTR的荧光素酶活性未改变。通过蛋白质免疫印迹法,Bcl-2显著降低,而Bax、细胞色素C和半胱天冬酶-3显著增加,且Bcl-2/Bax比值显著降低。这些结果表明,PCV2通过外泌体上调miR-125a-5p的表达,进而在mRNA和蛋白质水平抑制Bcl-2的表达,激活线粒体凋亡途径并诱导淋巴细胞凋亡。