Esposito G, Campa A, Pinto M, Simone G, Tabocchini M A, Belli M
Health and Technology Department, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Roma, Italy.
Radiat Prot Dosimetry. 2011 Feb;143(2-4):320-4. doi: 10.1093/rpd/ncq474. Epub 2010 Dec 15.
Adaptive response (AR) is a term that has been generally accepted to describe the ability of a low 'priming' radiation dose to decrease the cell response to a subsequent higher 'challenging' dose. The main proposed mechanisms to explain AR are: increased efficiency of DNA repair and induction of antioxidant enzymes. A model that considers a modulation of the efficiency of DNA repair activity and of the level of antioxidant enzymes, starting from the framework of a lethal-potentially lethal (LPL) model is proposed. The LPL model has been extended with the inclusion of the dynamic variables representing the efficiency of repair, the levels of radiation induced radicals and of antioxidant enzymes. The model used here is able to describe the protective effect of a priming dose. Moreover, in agreement with the data in the literature, the simulations show that the AR happens in given priming dose and priming dose-rate ranges only, and requires at least 4 h to develop. In order to get more insights into the role of cell-cell communication as factors affecting the AR, experimental studies were planned using sparse or confluent AG1522 cell monolayer. The results obtained after gamma irradiation suggest that cell density is a crucial factor for observing an AR.
适应性反应(AR)是一个已被普遍接受的术语,用于描述低“预激发”辐射剂量降低细胞对随后更高“挑战性”剂量反应的能力。解释AR的主要提出机制有:DNA修复效率提高和抗氧化酶的诱导。提出了一个模型,该模型从致死-潜在致死(LPL)模型的框架出发,考虑DNA修复活性效率和抗氧化酶水平的调节。LPL模型通过纳入代表修复效率、辐射诱导自由基水平和抗氧化酶水平的动态变量而得到扩展。这里使用的模型能够描述预激发剂量的保护作用。此外,与文献中的数据一致,模拟结果表明AR仅在给定的预激发剂量和预激发剂量率范围内发生,并且至少需要4小时才能显现。为了更深入了解细胞间通讯作为影响AR的因素的作用,计划使用稀疏或汇合的AG1522细胞单层进行实验研究。γ射线照射后获得的结果表明,细胞密度是观察到AR的关键因素。