Niu Bowen, Wu Jiang, Mu Hailong, Li Bo, Wu Chongyang, He Xin, Bai Chunling, Li Guangpeng, Hua Jinlian
1 College of Veterinary Medicine, Shaanxi Centre of Stem Cells Engineering & Technology, Key Lab for Animal Biotechnology of Agriculture Ministry of China, Northwest A&F University , Yangling, Shaanxi, China .
2 College of Agriculture, Guangdong Ocean University , Zhanjiang, China .
Rejuvenation Res. 2016 Apr;19(2):120-30. doi: 10.1089/rej.2015.1719. Epub 2016 Feb 1.
The regulation of spermatogonial stem cell (SSC) proliferation and self-renewal is a complex process. Several studies on the microRNA regulation of mammalian spermatogenesis have been reported. Here, we predicted miRNA targeting of Sirt1, and a dual luciferase experiment confirmed that miR-204 interacted with the Sirt1 3'-untranslated region (3'-UTR). The expression of miR-204 and Sirt1 in dairy goat testicles was investigated, and the results showed that the expression pattern of Sirt1 was similar to that of miR-204 in the temporal-spatial distribution. The over-expression of Sirt1 in goat SSCs can promote SSCs' self-renewal gene expression and cell proliferation. Furthermore, miRNA sequencing results showed that Sirt1 had a higher expression level in dairy goat CD49f(+) and CD90(+) SSCs, but the expression level of miR-204 was lower. In an in vitro assay, Sirt1 was significantly down-regulated in dairy goat SSCs when transfected with miR-204 mimics, indicating that Sirt1 was a target of miR-204 in the dairy goat. On the basis of the results of RT-qPCR, fluorescence-activated cell sorting (FACS), and western blotting, we found that the over-expression of Sirt1 in goat SSCs can promote cellular proliferation and change self-renewal and pluripotent gene expression. Thus, miR-204 was involved in the regulation of dairy goat SSCs proliferation via Sirt1.
精原干细胞(SSC)增殖和自我更新的调控是一个复杂的过程。已有多项关于哺乳动物精子发生的微小RNA调控的研究报道。在此,我们预测了靶向Sirt1的微小RNA,双荧光素酶实验证实miR-204与Sirt1的3'-非翻译区(3'-UTR)相互作用。我们研究了miR-204和Sirt1在奶山羊睾丸中的表达情况,结果表明Sirt1的表达模式在时空分布上与miR-204相似。在山羊精原干细胞中过表达Sirt1可促进精原干细胞自我更新基因的表达和细胞增殖。此外,微小RNA测序结果显示,Sirt1在奶山羊CD49f(+)和CD90(+)精原干细胞中的表达水平较高,但miR-204的表达水平较低。在体外实验中,当用miR-204模拟物转染奶山羊精原干细胞时,Sirt1显著下调,表明Sirt1是奶山羊中miR-204的靶点。基于逆转录-定量聚合酶链反应(RT-qPCR)、荧光激活细胞分选(FACS)和蛋白质印迹法的结果,我们发现山羊精原干细胞中Sirt1的过表达可促进细胞增殖并改变自我更新和多能基因的表达。因此,miR-204通过Sirt1参与了奶山羊精原干细胞增殖的调控。