Pacific Northwest National Laboratory, Richland, Washington, United States of America.
PLoS One. 2010 Nov 30;5(11):e14152. doi: 10.1371/journal.pone.0014152.
High doses of ionizing radiation result in biological damage; however, the precise relationships between long-term health effects, including cancer, and low-dose exposures remain poorly understood and are currently extrapolated using high-dose exposure data. Identifying the signaling pathways and individual proteins affected at the post-translational level by radiation should shed valuable insight into the molecular mechanisms that regulate dose-dependent responses to radiation.
We have identified 7117 unique phosphopeptides (2566 phosphoproteins) from control and irradiated (2 and 50 cGy) primary human skin fibroblasts 1 h post-exposure. Semi-quantitative label-free analyses were performed to identify phosphopeptides that are apparently altered by radiation exposure. This screen identified phosphorylation sites on proteins with known roles in radiation responses including TP53BP1 as well as previously unidentified radiation-responsive proteins such as the candidate tumor suppressor SASH1. Bioinformatic analyses suggest that low and high doses of radiation affect both overlapping and unique biological processes and suggest a role for MAP kinase and protein kinase A (PKA) signaling in the radiation response as well as differential regulation of p53 networks at low and high doses of radiation.
Our results represent the most comprehensive analysis of the phosphoproteomes of human primary fibroblasts exposed to multiple doses of ionizing radiation published to date and provide a basis for the systems-level identification of biological processes, molecular pathways and individual proteins regulated in a dose dependent manner by ionizing radiation. Further study of these modified proteins and affected networks should help to define the molecular mechanisms that regulate biological responses to radiation at different radiation doses and elucidate the impact of low-dose radiation exposure on human health.
高剂量的电离辐射会导致生物损伤;然而,长期健康影响(包括癌症)与低剂量暴露之间的精确关系仍知之甚少,目前正在使用高剂量暴露数据进行推断。确定在翻译后水平上受辐射影响的信号通路和个体蛋白质,应该为调节辐射剂量依赖性反应的分子机制提供有价值的见解。
我们从对照和照射(2 和 50 cGy)的原代人皮肤成纤维细胞中鉴定出 7117 个独特的磷酸肽(2566 个磷酸蛋白),暴露后 1 小时。进行半定量无标记分析以鉴定明显受辐射暴露改变的磷酸肽。该筛选鉴定了在辐射反应中具有已知作用的蛋白质上的磷酸化位点,包括 TP53BP1 以及以前未识别的辐射反应性蛋白质,如候选肿瘤抑制因子 SASH1。生物信息学分析表明,低剂量和高剂量的辐射都会影响重叠和独特的生物过程,并表明 MAP 激酶和蛋白激酶 A(PKA)信号在辐射反应中以及在低剂量和高剂量辐射下 p53 网络的差异调节中的作用。
我们的结果代表了迄今为止对暴露于多种剂量电离辐射的人类原代成纤维细胞的磷酸蛋白质组进行的最全面分析,并为系统水平鉴定受电离辐射以剂量依赖方式调节的生物过程、分子途径和个体蛋白质提供了基础。进一步研究这些修饰蛋白和受影响的网络应该有助于定义调节不同辐射剂量下生物对辐射反应的分子机制,并阐明低剂量辐射暴露对人类健康的影响。