Kuroha Kazushige, Dočkal Ivana, Radović Uroš, Nakajima Kuniko, Hoshi Ikue, Matsuda Shion, Kojitani Noriko, Ohbo Kazuyuki, Tomizawa Shin-Ichi
Department of Histology and Cell Biology, Yokohama City University School of Medicine, Yokohama 236-0004, Japan.
Development. 2025 Jan 15;152(2). doi: 10.1242/dev.204239. Epub 2025 Jan 16.
Cryptorchidism is the most frequent congenital defect in newborn males characterized by the absence of the testis from the scrotum. Approximately 90% of individuals with untreated bilateral cryptorchidism exhibit azoospermia due to defective spermatogenesis in the affected testis. Although abnormal spermatogonial stem cell maintenance or differentiation is suggested to cause germ cell degeneration in the cryptorchid testis, the underlying molecular mechanisms remain unclear. Here, we profiled spermatogonial epigenetic landscapes using surgically induced cryptorchid testis in the mouse. We show that cryptorchidism leads to alterations in local, but not global, H3K27me3 and H3K9me3 in undifferentiated spermatogonia. Of these, the loss of H3K27me3 was correlated with activation of developmental and proapoptotic pathway genes that are repressed by the polycomb machinery in germ cells. Cryptorchid spermatogonia exhibit an increase of the H3K27me3 demethylases KDM6A and KMD6B. Furthermore, we reveal that an increased temperature leads to Kdm6a/b upregulation in germline stem cells cultured in vitro. Thus, our study suggests that temperature-dependent histone demethylation may induce mRNA dysregulation due to the partial loss of H3K27me3 in spermatogonia.
隐睾症是新生男婴中最常见的先天性缺陷,其特征是阴囊中没有睾丸。约90%未经治疗的双侧隐睾症患者由于患侧睾丸生精功能缺陷而表现为无精子症。尽管有研究表明,异常的精原干细胞维持或分化会导致隐睾症睾丸中的生殖细胞退化,但其潜在的分子机制仍不清楚。在此,我们利用手术诱导的小鼠隐睾症对精原细胞的表观遗传景观进行了分析。我们发现,隐睾症会导致未分化精原细胞中局部(而非整体)H3K27me3和H3K9me3的改变。其中,H3K27me3的缺失与发育和促凋亡途径基因的激活相关,这些基因在生殖细胞中受到多梳蛋白机制的抑制。隐睾症精原细胞中H3K27me3去甲基化酶KDM6A和KMD6B的表达增加。此外,我们还发现,温度升高会导致体外培养的生殖系干细胞中Kdm6a/b上调。因此,我们的研究表明,温度依赖性组蛋白去甲基化可能会由于精原细胞中H3K27me3的部分缺失而导致mRNA失调。