Ono T, Okada S
Mutat Res. 1976 Aug;36(2):213-222. doi: 10.1016/0027-5107(76)90008-7.
The radiosensitivity of DNA molecules in testicular cells from adult male mice in situ was 0.22 single-strand breks per 10(12) daltons of DNA per rad. This was significantly lower than the 0.6-0.7 for liver and thymus DNA, and was most likely attributable to a hypoxic condition of testicular cells in situ. Although a majority of the single-strand scissions was quickly rejoined, a significant extent of breaks remained without further rejoining. The presence of remaining breaks was demonstrated not only after 3-6 h of post-irradiation time, but also after irradiation at low dose rates. The remaining breaks might be a slow and/or non-reparable DNA damage.
成年雄性小鼠原位睾丸细胞中DNA分子的放射敏感性为每拉德每10¹²道尔顿DNA产生0.22个单链断裂。这显著低于肝脏和胸腺DNA的0.6 - 0.7,很可能归因于原位睾丸细胞的缺氧状态。虽然大多数单链断裂能迅速重新连接,但仍有相当一部分断裂未进一步重新连接。不仅在照射后3 - 6小时,而且在低剂量率照射后,都证实了剩余断裂的存在。剩余断裂可能是一种缓慢和/或不可修复的DNA损伤。