Henriksén K, Hakovirta H, Parvinen M
Department of Anatomy, University of Turku, Finland.
Int J Androl. 1995 Oct;18(5):256-62.
Two techniques have been combined for quantification of apoptotic germ cells in defined stages of the cycle of the seminiferous epithelium: the improved transillumination method and nonradioactive in-situ end-labelling of DNA (ISEL). Segments of rat seminiferous tubules were squashed between a microscope slide and coverslip, and the stage identified under a phase-contrast microscope. After fixation, apoptotic cells were detected by ISEL and scored per 1 mm tubule. In the normal testis apoptotic cells were found in all stages, the highest frequency occurring in stages XII-XIV (19 cells/mm). In short-term (24 and 48 h) experimentally cryptorchid testes, a significant increase in number of apoptotic germ cells was evident in all stages, except for VI and VIII. Apoptosis of germ cells was confirmed by electrophoresis of radioactively labelled DNA from stages VII-VIII and XIII-I. It is proposed that apoptosis is a means of eliminating the most sensitive germ cells after short-term experimental cryptorchidism.
改良透照法和DNA的非放射性原位末端标记法(ISEL)。将大鼠生精小管段夹在显微镜载玻片和盖玻片之间压片,并在相差显微镜下确定阶段。固定后,通过ISEL检测凋亡细胞,并按每1毫米小管进行计数。在正常睾丸中,各阶段均发现凋亡细胞,最高频率出现在第XII - XIV阶段(19个细胞/毫米)。在短期(24小时和48小时)实验性隐睾睾丸中,除了第VI和VIII阶段外,所有阶段凋亡生殖细胞数量均显著增加。通过对第VII - VIII阶段和第XIII - I阶段放射性标记DNA进行电泳,证实了生殖细胞的凋亡。有人提出,凋亡是短期实验性隐睾后消除最敏感生殖细胞的一种方式。