An in vitro system for experimentally induced cryptorchidism

被引:2
|
作者
Okugi, Kensuke [1 ]
Kuwahara, Natsuki [1 ]
Yanome, Natsumi [1 ]
Yamada, Kaito [1 ]
Ito, Takuma [1 ]
Takano, Atsushi [2 ]
Ohira, Shin [3 ]
Nagai, Atsushi [3 ]
Tone, Shigenobu [1 ]
机构
[1] Tokyo Denki Univ, Grad Sch Sci & Engn, Lab Mol Dev Biol, Hatoyama, Saitama 3500394, Japan
[2] RIKEN, Cluster Pioneering Res, Human Biomimet Syst RIKEN Hakubi Res Team, Wako, Saitama 3510198, Japan
[3] Kawasaki Med Sch, Dept Urol, 577 Matsushima, Kurashiki, Okayama 7010192, Japan
关键词
Spermatogenesis; Cryptorchidism; In vitro culture; Apoptosis; Acr-GFP mouse; GERM-CELL APOPTOSIS; SPERMATOGENIC CELLS; MOUSE; SPERM; DIFFERENTIATION; DEATH; HEAT; TIME;
D O I
10.1007/s00418-022-02078-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 degrees C, in accordance with in vivo surgery-mediated cryptorchidism, while spermatogenesis proceeded at 34 degrees 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 degrees 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 degrees C) suppresses DNA synthesis in spermatogenesis.
引用
收藏
页码:297 / 307
页数:11
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