Division of Germ Cell Biology, National Institute for Basic Biology, National Institutes of Natural Sciences, 5-1 Higashiyama, Myodaiji, Okazaki, 444-8787, Japan.
Department of Basic Biology, School of Life Science, Graduate University for Advanced Studies (Sokendai), 5-1 Higashiyama, Myodaiji, Okazaki, 444-8787, Japan.
Commun Biol. 2022 May 26;5(1):504. doi: 10.1038/s42003-022-03449-y.
Mammalian spermatogenesis is a heat-vulnerable process that occurs at low temperatures, and elevated testicular temperatures cause male infertility. However, the current reliance on in vivo assays limits their potential to detail temperature dependence and destructive processes. Using ex vivo cultures of mouse testis explants at different controlled temperatures, we found that spermatogenesis failed at multiple steps, showing sharp temperature dependencies. At 38 °C (body core temperature), meiotic prophase I is damaged, showing increased DNA double-strand breaks (DSBs) and compromised DSB repair. Such damaged spermatocytes cause asynapsis between homologous chromosomes and are eliminated by apoptosis at the meiotic checkpoint. At 37 °C, some spermatocytes survive to the late pachytene stage, retaining high levels of unrepaired DSBs but do not complete meiosis with compromised crossover formation. These findings provide insight into the mechanisms and significance of heat vulnerability in mammalian spermatogenesis.
哺乳动物精子发生是一个在低温下发生的易受热影响的过程,而睾丸温度升高会导致男性不育。然而,目前对体内检测的依赖限制了它们详细研究温度依赖性和破坏性过程的潜力。通过在不同控制温度下对小鼠睾丸组织外植体进行体外培养,我们发现精子发生在多个步骤中失败,表现出明显的温度依赖性。在 38°C(核心体温)下,减数分裂前期 I 受损,显示出 DNA 双链断裂(DSB)增加和 DSB 修复受损。这种受损的精母细胞导致同源染色体之间的联会失败,并在减数分裂检查点通过细胞凋亡被消除。在 37°C 时,一些精母细胞存活到粗线期晚期,保持高水平的未修复 DSB,但不能完成减数分裂,交叉形成受损。这些发现为哺乳动物精子发生中受热脆弱性的机制和意义提供了深入了解。