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睾丸特异性表达基因2在隐睾症模型中的表达模式及其在生精细胞凋亡中的作用。

Expression pattern of testis-specific expressed gene 2 in cryptorchidism model and its role in apoptosis of spermatogenic cells.

作者信息

Hu Tao, Wang Zhiyu, Zeng Fuqing, Chen Xiaochun, Gu Zhaohui, Zheng Liduan, Tong Qiangsong

机构信息

Department of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2010 Apr;30(2):193-7. doi: 10.1007/s11596-010-0212-3. Epub 2010 Apr 21.

Abstract

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.

摘要

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。

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