Institute of Comparative Medicine, Division of Cell Sciences, University of Glasgow Veterinary School, Glasgow, UK.
Endocrinology. 2010 May;151(5):2343-8. doi: 10.1210/en.2009-1333. Epub 2010 Mar 12.
Androgens act to stimulate spermatogenesis through androgen receptors (ARs) on the Sertoli cells and peritubular myoid cells. Specific ablation of the AR in either cell type will cause a severe disruption of spermatogenesis. To determine whether androgens can stimulate spermatogenesis through direct action on the peritubular myoid cells alone or whether action on the Sertoli cells is essential, we crossed hypogonadal (hpg) mice that lack gonadotrophins and intratesticular androgen with mice lacking ARs either ubiquitously (ARKO) or specifically on the Sertoli cells (SCARKO). These hpg.ARKO and hpg.SCARKO mice were treated with testosterone (T) or dihydrotestosterone (DHT) for 7 d and testicular morphology and cell numbers assessed. Androgen treatment did not affect Sertoli cell numbers in any animal group. Both T and DHT increased numbers of spermatogonia and spermatocytes in hpg mice, but DHT has no effect on germ cell numbers in hpg.SCARKO and hpg.ARKO mice. T increased germ cell numbers in hpg.SCARKO and hpg.ARKO mice, but this was associated with stimulation of FSH release. Results show that androgen stimulation of spermatogenesis requires direct androgen action on the Sertoli cells.
雄激素通过支持细胞和小管周肌样细胞上的雄激素受体 (AR) 作用来刺激精子发生。这两种细胞类型中 AR 的特异性缺失都会导致精子发生严重破坏。为了确定雄激素是否可以通过对小管周肌样细胞的直接作用单独刺激精子发生,或者对支持细胞的作用是否是必需的,我们将缺乏促性腺激素和睾丸内雄激素的低促性腺激素血症 (hpg) 小鼠与泛 AR 缺失 (ARKO) 或特异性支持细胞 AR 缺失 (SCARKO) 的小鼠进行杂交。这些 hpg.ARKO 和 hpg.SCARKO 小鼠用睾酮 (T) 或二氢睾酮 (DHT) 处理 7 天,并评估睾丸形态和细胞数量。雄激素处理不会影响任何动物组的支持细胞数量。T 和 DHT 均增加了 hpg 小鼠精原细胞和精母细胞的数量,但 DHT 对 hpg.SCARKO 和 hpg.ARKO 小鼠的生殖细胞数量没有影响。T 增加了 hpg.SCARKO 和 hpg.ARKO 小鼠的生殖细胞数量,但这与 FSH 释放的刺激有关。结果表明,雄激素刺激精子发生需要雄激素对支持细胞的直接作用。