Rijntjes Eddy, Gomes Marcos L M, Zupanič Nina, Swarts Hans J M, Keijer Jaap, Teerds Katja J
Human and Animal Physiology, Department of Animal Sciences, Wageningen UniversityWageningen, Netherlands.
Institut für Experimentelle Endokrinologie, Charité-Universitätsmedizin BerlinBerlin, Germany.
Front Physiol. 2017 May 23;8:323. doi: 10.3389/fphys.2017.00323. eCollection 2017.
Transient neonatal 6-propyl-2-thiouracil (PTU) induced hypothyroidism affects Leydig and Sertoli cell numbers in the developing testis, resulting in increased adult testis size. The hypothyroid condition was thought to be responsible, an assumption questioned by studies showing that uninterrupted fetal/postnatal hypothyroidism did not affect adult testis size. Here, we investigated effects of transient hypothyroidism on Leydig and Sertoli cell development, employing a perinatal iodide-deficient diet in combination with sodium perchlorate. This hypothyroidism inducing diet was continued until days 1, 7, 14, or 28 postpartum (pp) respectively, when the rats were switched to a euthyroid diet and followed up to adulthood. Continuous euthyroid and hypothyroid, and neonatal PTU-treated rats switched to the euthyroid diet at 28 days pp, were included for comparison. No effects on formation of the adult-type Leydig cell population or on Sertoli cell proliferation and differentiation were observed when the diet switched at/or before day 14 pp. However, when the diet was discontinued at day 28 pp, Leydig cell development was delayed similarly to what was observed in chronic hypothyroid rats. Surprisingly, Sertoli cell proliferation was 6- to 8-fold increased 2 days after the diet switch and remained elevated the next days. In adulthood, Sertoli cell number per seminiferous tubule cross-section and consequently testis weight was increased in this group. These observations implicate that increased adult testis size in transiently hypothyroid rats is not caused by the hypothyroid condition , but originates from augmented Sertoli cell proliferation as a consequence of rapid normalization of thyroid hormone concentrations.
短暂性新生儿6-丙基-2-硫氧嘧啶(PTU)诱导的甲状腺功能减退会影响发育中睾丸的睾丸间质细胞和支持细胞数量,导致成年睾丸体积增大。甲状腺功能减退状态被认为是原因所在,但一些研究对这一假设提出了质疑,这些研究表明,持续的胎儿期/出生后甲状腺功能减退并不会影响成年睾丸体积。在此,我们采用围产期缺碘饮食并结合高氯酸钠,研究短暂性甲状腺功能减退对睾丸间质细胞和支持细胞发育的影响。这种诱导甲状腺功能减退的饮食持续到产后第1、7、14或28天,之后大鼠改为正常甲状腺功能饮食并随访至成年。为作比较,纳入了持续正常甲状腺功能和甲状腺功能减退的大鼠,以及在产后28天改为正常甲状腺功能饮食的新生儿PTU处理大鼠。当在产后14天及以前改变饮食时,未观察到对成年型睾丸间质细胞群体的形成或对支持细胞增殖及分化有影响。然而,当在产后28天停止这种饮食时,睾丸间质细胞的发育延迟,与慢性甲状腺功能减退大鼠中观察到的情况相似。令人惊讶的是,饮食转换后2天,支持细胞增殖增加了6至8倍,并在接下来的几天内保持升高。成年后,该组每生精小管横截面积的支持细胞数量增加,因此睾丸重量增加。这些观察结果表明,短暂性甲状腺功能减退大鼠成年睾丸体积增大并非由甲状腺功能减退状态引起,而是源于甲状腺激素浓度快速恢复正常后支持细胞增殖增加。