Zhou X, Kudo A, Kawakami H, Hirano H
Department of Anatomy, Kyorin University School of Medicine, Tokyo, Japan.
Anat Rec. 1996 Jul;245(3):509-18. doi: 10.1002/(SICI)1097-0185(199607)245:3<509::AID-AR7>3.0.CO;2-M.
Determination of the cellular distribution of the androgen receptor (AR) in testicular cells is necessary for understanding the mode of AR action in the testis. We here investigated immunohistochemically the localization of AR by use of anti-human AR polyclonal antibody NH27, with special reference to the AR in germ cells in the developing mouse testis.
ICR mouse testes taken from day 14 post coitum (p.c.) to day 56 post partum (p.p) were used for AR immunohistochemistry by the routine immunoperoxidase method at the light microscopic level and the pre-embedding method at the electron microscopic level.
On day 14 p.c., AR immunoreactivity was present in nuclei of prospermatogonia but not in those of Sertoli cells or interstitial cells. On day 14 p.p., the AR was detected in the nuclei of spermatogonia, Sertoli cells, and myoid cells. AR immunoreactivity in nuclei of Leydig cells appeared on day 21 p.p. In the mature mouse testis, the AR was present in the nuclei of spermatogonia, Sertoli cells, myoid cells, and Leydig cells.
AR was present both in germ cells and in somatic cells during fetal and postnatal development of the mouse testis. In the fetal testis, AR was localized exclusively in prospermatogonia and spermatogonia, suggesting that androgen may act directly on germ cells during prespermatogenesis and the early stage of spermatogenesis. Based on the fact that AR is expressed in Sertoli cells, myoid cells, and Leydig cells around the onset of spermatogenesis, the regulation of AR expression in the germ cells seems to be different from that in the somatic cells. Furthermore, our present data suggest the ultrastructural localization in nuclei of mouse testicular cells is similar to that of some other steroid receptors, both in germ cells and somatic cells.
确定雄激素受体(AR)在睾丸细胞中的细胞分布对于理解AR在睾丸中的作用模式至关重要。我们在此利用抗人AR多克隆抗体NH27,通过免疫组织化学方法研究AR的定位,特别关注发育中小鼠睾丸生殖细胞中的AR。
采用常规免疫过氧化物酶法在光镜水平以及包埋前法在电镜水平,对受孕后第14天(p.c.)至出生后第56天(p.p.)的ICR小鼠睾丸进行AR免疫组织化学检测。
在受孕后第14天,AR免疫反应性存在于精原细胞的细胞核中,而在支持细胞或间质细胞的细胞核中未检测到。在出生后第14天,在精原细胞、支持细胞和肌样细胞的细胞核中检测到AR。在出生后第21天,在Leydig细胞的细胞核中出现AR免疫反应性。在成熟小鼠睾丸中,AR存在于精原细胞、支持细胞、肌样细胞和Leydig细胞的细胞核中。
在小鼠睾丸的胎儿期和出生后发育过程中,AR既存在于生殖细胞中,也存在于体细胞中。在胎儿睾丸中,AR仅定位于精原细胞和精原细胞,这表明雄激素可能在精子发生前期和精子发生早期直接作用于生殖细胞。基于AR在精子发生开始时在支持细胞、肌样细胞和Leydig细胞中表达这一事实,生殖细胞中AR表达的调节似乎与体细胞中的不同。此外,我们目前的数据表明,小鼠睾丸细胞核中的超微结构定位在生殖细胞和体细胞中与其他一些类固醇受体相似。