Hu Tao, Wang Zhiyu, Zeng Fuqing, Chen Xiaochun, Gu Zhaohui, Zheng Liduan, Tong Qiangsong
Department of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
J Huazhong Univ Sci Technolog Med Sci. 2010 Apr;30(2):193-7. doi: 10.1007/s11596-010-0212-3. Epub 2010 Apr 21.
In our previous study, we identified a novel testis-specific expressed gene 2 (TSEG-2) from mouse testis. To further investigate its functions, 35 male Balb/c mice (8 weeks old) were divided into cryptorchidism group (n=20), sham group (n=10), and control group (n=5). In cryptorchidism group, the right testes were anchored to the inner lateral abdominal wall. In situ hybridization (ISH) was applied to measure the localization of TSEG-2 in mouse testis. Real-time quantitative PCR was performed to detect the expression of TSEG-2 gene. Meanwhile, under the mediation of polyethylenimine (PEI), the recombinant vector pEGFP-TSEG-2 (n=5) or empty vector (mock, n=5) was transfected into the testis of male mice. The transfection efficiencies were measured under a fluorescence microscope. The apoptosis of spermatogenic cells was detected by terminal deoxynuleotidyl-mediated nick end labeling (TUNEL). The results showed that TSEG-2 was expressed in convoluted seminiferous tubules, more precisely, in spermatogonia and spermatocytes. As compared with sham and control groups, the TSEG-2 transcription was significantly enhanced (P<0.05) and was correlated with apoptosis of spermatogenic cells in cryptorchid testes (P<0.05). PEI was efficient in mediating transfection of TSEG-2 into seminiferous tubules of testis. One week post-transfection, intratesticular injection of TSEG-2 resulted in increased apoptosis of spermatogenic cells in vivo (P<0.05). These results indicate that TSEG-2 may participate in the apoptosis of spermatogenic cells and the pathogenesis of cryptorchidism.
在我们之前的研究中,我们从小鼠睾丸中鉴定出一个新的睾丸特异性表达基因2(TSEG-2)。为了进一步研究其功能,将35只8周龄的雄性Balb/c小鼠分为隐睾组(n = 20)、假手术组(n = 10)和对照组(n = 5)。在隐睾组中,将右侧睾丸固定于腹内侧壁。应用原位杂交(ISH)检测TSEG-2在小鼠睾丸中的定位。进行实时定量PCR检测TSEG-2基因的表达。同时,在聚乙烯亚胺(PEI)介导下,将重组载体pEGFP-TSEG-2(n = 5)或空载体(对照,n = 5)转染到雄性小鼠睾丸中。在荧光显微镜下测量转染效率。采用末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)检测生精细胞凋亡。结果显示,TSEG-2在曲细精管中表达,更确切地说是在精原细胞和精母细胞中表达。与假手术组和对照组相比,隐睾睾丸中TSEG-2转录显著增强(P < 0.05),且与生精细胞凋亡相关(P < 0.05)。PEI能有效地介导TSEG-2转染到睾丸曲细精管中。转染后1周,睾丸内注射TSEG-2导致体内生精细胞凋亡增加(P < 0.05)。这些结果表明,TSEG-2可能参与生精细胞凋亡及隐睾症的发病机制。