Laboratory of Signal Transduction, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Cancer Res. 2010 Feb 1;70(3):957-67. doi: 10.1158/0008-5472.CAN-09-1562. Epub 2010 Jan 19.
Acute endothelial cell apoptosis and microvascular compromise couple gastrointestinal tract irradiation to reproductive death of intestinal crypt stem cell clonogens (SCCs) following high-dose radiation. Genetic or pharmacologic inhibition of endothelial apoptosis prevents intestinal damage, but as the radiation dose is escalated, SCCs become directly susceptible to an alternate cell death mechanism, mediated via ceramide synthase (CS)-stimulated de novo synthesis of the proapoptotic sphingolipid ceramide, and p53-independent apoptosis of crypt SCCs. We previously reported that ataxia-telangiectasia mutated deficiency resets the primary radiation lethal pathway, allowing CS-mediated apoptosis at the low-dose range of radiation. The mechanism for this event, termed target reordering, remains unknown. Here, we show that inactivation of DNA damage repair pathways signals CS-mediated apoptosis in crypt SCCs, presumably via persistent unrepaired DNA double-strand breaks (DSBs). Genetic loss of function of sensors and transducers of DNA DSB repair confers the CS-mediated lethal pathway in intestines of sv129/B6Mre11(ATLD1/ATLD1) and C57BL/6(Prkdc/SCID) (severe combined immunodeficient) mice exposed to low-dose radiation. In contrast, CS-mediated SCC lethality was mitigated in irradiated gain-of-function Rad50(s/s) mice, and epistasis studies order Rad50 upstream of Mre11. These studies suggest unrepaired DNA DSBs as causative in target reordering in intestinal SCCs. As such, we provide an in vivo model of DNA damage repair that is standardized, can be exploited to understand allele-specific regulation in intact tissue, and is pharmacologically tractable.
急性内皮细胞凋亡和微血管损伤将胃肠道辐射与肠隐窝干细胞克隆形成细胞(SCC)的生殖死亡联系起来,这是由于高剂量辐射所致。内皮细胞凋亡的遗传或药物抑制可防止肠道损伤,但随着辐射剂量的增加,SCC 直接易受另一种细胞死亡机制的影响,该机制通过神经酰胺合酶(CS)刺激从头合成促凋亡鞘脂神经酰胺和 p53 非依赖性隐窝 SCC 凋亡来介导。我们之前报道过,共济失调毛细血管扩张突变缺陷重置了主要的辐射致死途径,允许 CS 介导的凋亡发生在低剂量辐射范围内。这种称为靶标重新排序的事件的机制尚不清楚。在这里,我们表明,DNA 损伤修复途径的失活会导致隐窝 SCC 中的 CS 介导的细胞凋亡,可能是通过持续未修复的 DNA 双链断裂(DSB)。DNA 双链断裂修复传感器和转导器的遗传功能丧失赋予了 sv129/B6Mre11(ATLD1/ATLD1)和 C57BL/6(Prkdc/SCID)(严重联合免疫缺陷)小鼠暴露于低剂量辐射时 CS 介导的致命途径。相比之下,CS 介导的 SCC 致死性在辐射功能获得性 Rad50(s/s)小鼠中得到缓解,并且上位性研究将 Rad50 置于 Mre11 上游。这些研究表明未修复的 DNA DSB 是肠道 SCC 中靶标重新排序的原因。因此,我们提供了一种体内 DNA 损伤修复模型,该模型具有标准化、可用于理解完整组织中等位基因特异性调控的特点,并且具有药物可操作性。