Chi Z-H, Feng W-Y, Gao H-L, Zheng W, Huang L, Wang Z-Y
Department of Histology and Embryology, China Medical University, Shenyang, PR China.
Histol Histopathol. 2009 Jan;24(1):25-30. doi: 10.14670/HH-24.25.
The aim of the present study was to investigate the relation of the spatial distribution between ZNT7 and chelatable zinc ions in the mouse testis. Immunohistochemical results demonstrated a wide distribution of ZNT7 in both seminiferous tubules and interstitial tissues of the testis. The spermatocytes and spermatids in the seminiferous tubules showed strong ZNT7 immunoreactivity whereas zinc autometallographic (AMG) staining was absent. Spermatozoa showed a high level of free zinc, but were void of ZNT7 immunoreactivity. No ZNT7 immunoreactivity and AMG grains were found in spermatogonia. Both ZNT7 and chelatable zinc were detected in Sertoli and Leydig cells. Furthermore, double immunofluorescence study demonstrated that the ZNT7 staining overlapped with that of TGN38 (a trans-Golgi marker), suggesting that ZNT7 was localized in the Golgi apparatus in the ZNT7-positive cells. In conclusion, ZNT7 and chelatable zinc were distributed in different cell populations except for Sertoli and Leydig cells in the mouse testis. ZNT7 may be involved in zinc transportation into the Golgi apparatus for protein packaging in the mouse testis.
本研究的目的是探究小鼠睾丸中锌转运体7(ZNT7)与可螯合锌离子的空间分布关系。免疫组化结果显示,ZNT7在睾丸的生精小管和间质组织中均广泛分布。生精小管中的精母细胞和精子细胞显示出较强的ZNT7免疫反应性,而锌自身金相(AMG)染色阴性。精子显示出高水平的游离锌,但缺乏ZNT7免疫反应性。精原细胞中未发现ZNT7免疫反应性和AMG颗粒。支持细胞和间质细胞中均检测到ZNT7和可螯合锌。此外,双重免疫荧光研究表明,ZNT7染色与TGN38(一种反式高尔基体标记物)的染色重叠,表明ZNT7定位于ZNT7阳性细胞的高尔基体中。总之,在小鼠睾丸中,除支持细胞和间质细胞外,ZNT7和可螯合锌分布于不同的细胞群体中。ZNT7可能参与小鼠睾丸中锌向高尔基体的转运,以进行蛋白质包装。