Okugi Kensuke, Kuwahara Natsuki, Yanome Natsumi, Yamada Kaito, Ito Takuma, Takano Atsushi, Ohira Shin, Nagai Atsushi, Toné Shigenobu
Laboratory of Molecular Developmental Biology, Graduate School of Science and Engineering, Tokyo Denki University, Hatoyama, Saitama, 350-0394, Japan.
Human Biomimetic System RIKEN Hakubi Research Team, Cluster for Pioneering Research, RIKEN, Wako, Saitama, 351-0198, Japan.
Histochem Cell Biol. 2022 Mar;157(3):297-307. doi: 10.1007/s00418-022-02078-0. Epub 2022 Feb 21.
Cryptorchidism is one of the most common abnormalities of male sexual development, and is characterized by the failure of the testis to descend into the scrotum. Despite extensive studies of cryptorchidism over the past century, the mechanisms for temperature-induced germ-cell loss are not well understood. All of the main cell types in the testis are believed to be affected by the elevated testis temperature induced by cryptorchidism. The cooler temperature in the special environment of the scrotum is required for maintaining optional conditions for normal spermatogenesis. Many studies reported that experimentally induced cryptorchidism caused germ cell apoptosis and suppressed spermatogenesis. However, other factors including hormones must also be examined for cryptorchidism. To explore the mechanism for cryptorchidism, in vitro cultures of testes have been used, but complete spermatogenesis using in vitro methods was not accomplished until 2011. In 2011, Sato et al. (Nature, 471, 504-507) reported the in vitro production of functional sperm in cultured neonatal mouse testes. Using this in vitro system, for the first time, we report that spermatogenesis was abrogated at 37 °C, in accordance with in vivo surgery-mediated cryptorchidism, while spermatogenesis proceeded at 34 °C in cultured testes. This result clearly showed that temperature is the sole determinant of cryptorchidism. Moreover, we found that spermatogenesis was arrested before early spermatocytes at 37 °C. In conclusion, using our in vitro system, we have demonstrated that (1) temperature is the determining factor for cryptorchidism, and (2) higher temperature (37 °C) suppresses DNA synthesis in spermatogenesis.
隐睾症是男性性发育最常见的异常之一,其特征是睾丸未能降入阴囊。尽管在过去一个世纪对隐睾症进行了广泛研究,但温度诱导生殖细胞丢失的机制仍未完全明确。睾丸中的所有主要细胞类型都被认为会受到隐睾症导致的睾丸温度升高的影响。阴囊特殊环境中的较低温度是维持正常精子发生的最佳条件所必需的。许多研究报告称,实验性诱导的隐睾症会导致生殖细胞凋亡并抑制精子发生。然而,对于隐睾症,还必须研究包括激素在内的其他因素。为了探索隐睾症的机制,人们使用了睾丸的体外培养,但直到2011年才通过体外方法实现完全的精子发生。2011年,佐藤等人(《自然》,471卷,504 - 507页)报告了在培养的新生小鼠睾丸中体外产生功能性精子的情况。利用这个体外系统,我们首次报告,与体内手术介导的隐睾症一致,在37°C时精子发生被废除,而在培养的睾丸中,34°C时精子发生仍在进行。这一结果清楚地表明温度是隐睾症的唯一决定因素。此外,我们发现精子发生在37°C时在早期精母细胞之前就被阻断。总之,利用我们的体外系统,我们证明了(1)温度是隐睾症的决定因素,(2)较高温度(37°C)抑制精子发生中的DNA合成。