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隐睾症可挽救幼年精原细胞耗竭(jsd)小鼠的精原细胞分化。

Cryptorchidism rescues spermatogonial differentiation in juvenile spermatogonial depletion (jsd) mice.

作者信息

Shetty Gunapala, Weng Connie C Y

机构信息

Department of Experimental Radiation Oncology, The University of Texas M D Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Endocrinology. 2004 Jan;145(1):126-33. doi: 10.1210/en.2003-0928. Epub 2003 Sep 18.

Abstract

Male mice homozygous for jsd mutation undergo an initial wave of spermatogenesis, but spermatogonial differentiation ceases a few weeks after birth; at that point the tubules show only type A spermatogonia and Sertoli cells. To test whether testicular descent into the scrotum contributes to the block in spermatogonial differentiation, jsd mutant (jsd/jsd) mice were bilaterally cryptorchidized at the age of 4 wk. Surprisingly, 8 wk later, germ cell differentiation was maintained in 98% of the tubules, a rate that fell to 13.5% in mice without surgery. The testis weight and the degree of spermatogenesis in cryptorchidized normal (jsd/+) and jsd mutant mice were almost identical. Furthermore, germ cell differentiation was also restored in almost all the tubules in 20-wk- and 70-wk-old jsd mutant testis unilaterally cryptorchidized 8 wk earlier, whereas the contralateral scrotal testis in these mice showed differentiation in only 6% of tubules. In irradiated LBNF1 rats, which have a block in spermatogonial differentiation similar to that in jsd mutant mice, unilateral cryptorchidism produced a small but significant increase in the percentage of differentiated tubules. In both of these models, the intratesticular levels of testosterone in the cryptorchidized testes were still above the physiological range, and the serum testosterone and LH levels were unchanged after bilateral or unilateral cryptorchidization. Cryptorchidism also did not alter serum FSH levels after bilateral and unilateral cryptorchidism in jsd mutant mice and irradiated rats, respectively. We conclude that cryptorchidism reverses the phenotype in jsd mutant mice. The findings show for the first time that spermatogenesis in rodents, and spermatogonial differentiation in particular, is sensitive to reduced scrotal temperature. Furthermore, we conclude that in jsd mutant mice spermatogonial differentiation is inhibited by testosterone only at the normal scrotal temperature.

摘要

jsd突变纯合子雄性小鼠会经历一波初始精子发生过程,但精原细胞分化在出生后几周就会停止;此时,曲细精管中仅显示A型精原细胞和支持细胞。为了测试睾丸降至阴囊是否会导致精原细胞分化受阻,对4周龄的jsd突变(jsd/jsd)小鼠进行双侧隐睾手术。令人惊讶的是,8周后,98%的曲细精管中生殖细胞分化得以维持,而未做手术的小鼠这一比例降至13.5%。隐睾的正常(jsd/+)和jsd突变小鼠的睾丸重量和精子发生程度几乎相同。此外,在8周前进行单侧隐睾手术的20周龄和70周龄jsd突变睾丸中,几乎所有曲细精管中的生殖细胞分化也得以恢复,而这些小鼠对侧阴囊内的睾丸仅6%的曲细精管显示有分化。在与jsd突变小鼠精原细胞分化受阻情况相似的经辐射的LBNF1大鼠中,单侧隐睾使分化曲细精管的百分比有小幅但显著的增加。在这两种模型中,隐睾睾丸内的睾酮水平仍高于生理范围,双侧或单侧隐睾后血清睾酮和促黄体生成素水平未发生变化。在jsd突变小鼠和经辐射的大鼠中,双侧和单侧隐睾后隐睾症也未改变血清促卵泡生成素水平。我们得出结论,隐睾症可逆转jsd突变小鼠的表型。这些发现首次表明,啮齿动物的精子发生,尤其是精原细胞分化,对阴囊温度降低敏感。此外,我们得出结论,在jsd突变小鼠中,仅在正常阴囊温度下,睾酮才会抑制精原细胞分化。

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