Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.
Asian J Androl. 2012 Nov;14(6):884-9. doi: 10.1038/aja.2012.71. Epub 2012 Sep 24.
Cold-inducible RNA-binding protein (CIRP) is an RNA-binding protein that is expressed in normal testes and downregulated after heat stress caused by cryptorchidism, varicocele or environmental temperatures. The purpose of this study was to investigate the functions of CIRP in the testes. We employed RNAi technique to knock down the expression of CIRP in the testes, and performed haematoxylin and eosin staining to evaluate morphological changes following knockdown. Germ cell apoptosis was examined by terminal deoxynucleotidal transferase-mediated dUTP nick end labelling (TUNEL) assay, and mitogen-activated protein kinase (MAPK) signalling pathways were investigated by Western blotting to determine the possible mechanism of apoptosis. We found that using siRNA is a feasible and reliable method for knocking down gene expression in the testes. Compared to controls, the mean seminiferous tubule diameter (MSTD) and the thickness of the germ cell layers decreased following siRNA treatment, whereas the percentage of apoptotic seminiferous tubules increased. The p44/p42, p38 and SAPK/JNK MAPK pathways were activated after downregulation of CIRP. In conclusion, we discovered that downregulation of CIRP resulted in increased germ cell apoptosis, possibly via the activation of the p44/p42, p38 and SAPK/JNK MAPK pathways.
冷诱导 RNA 结合蛋白(CIRP)是一种在正常睾丸中表达的 RNA 结合蛋白,在隐睾、精索静脉曲张或环境温度引起的热应激后下调。本研究旨在探讨 CIRP 在睾丸中的功能。我们采用 RNAi 技术敲低睾丸中 CIRP 的表达,并进行苏木精和伊红染色,以评估敲低后的形态学变化。通过末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记(TUNEL)检测评估生精细胞凋亡,通过 Western blot 检测丝裂原激活蛋白激酶(MAPK)信号通路,以确定凋亡的可能机制。我们发现,使用 siRNA 是一种可行且可靠的方法,可以敲低睾丸中的基因表达。与对照组相比,siRNA 处理后平均生精小管直径(MSTD)和生精细胞层厚度减小,而凋亡生精小管的比例增加。CIRP 下调后 p44/p42、p38 和 SAPK/JNK MAPK 途径被激活。总之,我们发现下调 CIRP 导致生精细胞凋亡增加,可能通过激活 p44/p42、p38 和 SAPK/JNK MAPK 途径。