Department of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Department of Pediatric Urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Andrology. 2020 Sep;8(5):1398-1408. doi: 10.1111/andr.12788. Epub 2020 Apr 13.
Cryptorchidism is known to impair spermatogenesis. The blood-testis barrier (BTB) becomes defined in seminiferous tubules around puberty and provides a suitable environment for germ cells. Little is known about the BTB in undescended testes (UDT).
To determine the role of BTB during puberty in UDT using a non-surgical cryptorchid rat model.
Unilateral cryptorchid male rats were intraperitoneally injected with non-steroidal antiandrogen during intrauterine development; the testes were harvested at 4, 5, and 6 weeks after birth. Testicular histology, expression levels of the BTB proteins (claudin-11, occludin, zonula occludens-1), and apoptotic cells were evaluated by immunohistochemistry, Western blotting, and TUNEL assay. The functionality of the BTB was investigated by electron microscopy using the lanthanum tracer method.
The testicular histology of undescended testes 6 weeks after birth showed maturation arrest at the spermatocyte level. The BTB protein distributions were altered in the UDT, with a noticeable difference in claudin-11(CLDN11) localization from 4 to 5 weeks after birth between control and UDT samples. BTB protein levels were similar. More apoptotic germ cells were detected in the adluminal compartment of tubules in the UDT than in the control testes. Electron microscopy showed that the lanthanum tracer was limited to the BTB of control testes, whereas it penetrated the BTB of UDT.
Here, loss of normal BTB function and impaired spermatogenesis were observed in UDT during puberty. CLDN11 is a pivotal tight junction protein belonging to the BTB. Tight junctions are considered as essential for normal spermatogenesis, and abnormal CLDN11 organization may cause UDT-associated male infertility.
CLDN11 disorganization within the BTB may cause spermatogenic impairment, possibly by limiting the BTB function.
隐睾会损害精子发生。血睾屏障(BTB)在青春期左右在精曲小管中形成,为生殖细胞提供适宜的环境。对于未降睾丸(UDT)中的 BTB 知之甚少。
使用非手术性隐睾大鼠模型确定青春期 UDT 中 BTB 的作用。
在子宫内发育期间,单侧隐睾雄性大鼠腹膜内注射非甾体类抗雄激素;在出生后 4、5 和 6 周收获睾丸。通过免疫组织化学、Western blot 和 TUNEL 检测评估睾丸组织学、BTB 蛋白(claudin-11、occludin、zonula occludens-1)的表达水平和凋亡细胞。使用镧示踪剂法通过电子显微镜研究 BTB 的功能。
出生后 6 周未降睾丸的睾丸组织学显示在精母细胞水平上成熟停滞。UDT 中的 BTB 蛋白分布发生改变,出生后 4 至 5 周时 CLDN11 的定位在对照组和 UDT 样本之间有明显差异。BTB 蛋白水平相似。在 UDT 的管腔腔中检测到更多的凋亡生殖细胞,而在对照睾丸中则较少。电子显微镜显示,镧示踪剂仅局限于对照睾丸的 BTB,而在 UDT 中则穿透了 BTB。
在这里,青春期 UDT 中观察到正常 BTB 功能丧失和精子发生受损。CLDN11 是属于 BTB 的重要紧密连接蛋白。紧密连接被认为对正常精子发生至关重要,异常的 CLDN11 组织可能导致 UDT 相关的男性不育。
BTB 内 CLDN11 的组织紊乱可能导致精子发生受损,可能是通过限制 BTB 功能。