Douglas Stephens Surgical Research Group, Murdoch Children's Research Institute, Melbourne, Australia; Department of Paediatrics, University of Melbourne, Australia.
Douglas Stephens Surgical Research Group, Murdoch Children's Research Institute, Melbourne, Australia.
J Pediatr Surg. 2019 Aug;54(8):1654-1659. doi: 10.1016/j.jpedsurg.2018.12.011. Epub 2019 Jan 3.
Neonatal testicular germ cells/gonocytes, transform into stem cells for spermatogenesis during 'minipuberty', driving change in timing of surgery. This study examined gonocyte transformation in cryptorchid testes in children ≤18 months of age with unilateral, bilateral undescended testes (UDT), complete or partial androgen insensitivity syndrome (CAIS, PAIS) [3,4].
Testicular biopsies were taken from patients with unilateral or bilateral UDT, PAIS or CAIS, aged 10 days-18 months. These testicular sections underwent immunohistochemistry with antibodies (Oct4, Ki67, C-Kit, Sox9) followed by confocal imaging, cell counting and statistical analysis.
Both Sertoli cells/tubule and germ cells (GC)/tubule decreased with age, and % empty tubules (no GC) increased with age but with no significant differences between patient groups. Oct4 germ cells/tubule decreased with age. There are some GCs and Sertoli cells proliferating during the first year and most proliferating Oct4 germ cells (Oct4/Ki67) were located off tubular basement membrane.
Our study showed that Oct4 expression gradually decreased after minipuberty and transformation into spermatogonia. Germ cells and Sertoli cells undergo mitosis during the first 12 months although not abundantly. We propose that Oct4 gonocyte transformation into spermatogonia via proliferation and migration to the basement membrane may be delayed in UDT.
新生儿睾丸生殖细胞/精原细胞在“小青春期”转化为精子发生的干细胞,推动了手术时机的改变。本研究检查了≤18 个月龄单侧、双侧未降睾丸(UDT)、完全或部分雄激素不敏感综合征(CAIS、PAIS)[3,4]患儿隐睾睾丸中精原细胞的转化。
从单侧或双侧 UDT、PAIS 或 CAIS 患儿 10 天至 18 个月龄时取睾丸活检。这些睾丸切片用 Oct4、Ki67、C-Kit、Sox9 抗体进行免疫组织化学染色,然后进行共聚焦成像、细胞计数和统计分析。
随着年龄的增长,Sertoli 细胞/小管和生殖细胞(GC)/小管都减少,而%空小管(无 GC)随着年龄的增长而增加,但在患者组之间没有显著差异。Oct4 生殖细胞/小管随着年龄的增长而减少。在第一年有一些 GC 和 Sertoli 细胞增殖,大多数增殖的 Oct4 生殖细胞(Oct4/Ki67)位于管基底膜之外。
我们的研究表明,Oct4 表达在小青春期后逐渐下降,并转化为精原细胞。生殖细胞和 Sertoli 细胞在最初的 12 个月内经历有丝分裂,尽管不丰富。我们提出,Oct4 精原细胞通过增殖和向基底膜迁移转化为精原细胞可能在 UDT 中延迟。