Artiukhov V G, Trubitsyna M S, Nakvasina M A, Solov'eva E V, Lidokhova O V
Radiats Biol Radioecol. 2011 Jul-Aug;51(4):425-43.
Changes of DNA structural condition, the level of membrane Fas-receptor expression, caspase-3 functional activity, concentrations of Ca2+, p53 and cytochrome c proteins of human lymphocytes in dynamics of apoptosis development induced by UV-light (240-390 nm) at doses 151, 1510, 3020 J/m2 and reactive oxygen species (superoxide anion-radical, hydroxyl radicals, hydrogen peroxide, singlet oxygen) have been studied. UV-light and reactive oxygen species have been established to induce fragmentation of lymphocyte DNA after 20 h incubation of the modified cells. It has been shown, that the increase in the expression level of membrane death Fas-receptors is observed during 1-5 h after exposure oflymphocytes to UV-light and ROS compared with intact cells. Also revealed is augmentation of lymphocyte caspase-3 functional activity 4 h after generation of singlet oxygen, hydroxyl radical and hydrogen peroxide addition, as well as 8 and 24 and 6 and 8 h after UV-irradiation of the cells at doses 151 and 1510 J/m2, correspondingly. Using DNA-comet method made it possible to tape that DNA damages (single-strand breaks) appear 15-20 min after lymphocyte UV-irradiation at doses 1510 and 3020 J/m and addition of hydrogen peroxide in concentration 10(-6) mol/l (C1 type comet) and reach their maximum 6 h after modification of the cells (C2 and C3 type comets). It has been observed, that 6 h after exposure oflymphocytes to hydrogen peroxide and UV-light at doses 1510 and 3020 J/m2, the p53 level of investigated cells raises. It has also been shown that the higher level of calcium in lymphocyte cytosol in conditions of UV-light exposure (1510 J/m2) and exogenous generation of reactive oxygen species is caused by Ca2+ exit from intracellular depots as a result of activating the components of the phosphoinositide mechanism for transferring information into a cell. Ideas about correlation between alterations of the calcium level and initiation of programmed cellular destruction of human lymphocytes after exposure to UV-irradiation and ROS is proposed. The authors come to the conclusion about the leading role of receptor-mediated (Fas-dependent) caspase- and p53-dependent ways of realizing apoptosis oflymphocytes induced by UV-light at doses 151 and 1510 J/m2 and active oxygen metabolites. The pattern of the possible intracellular events leading to apoptotic destruction of lymphocytes after their UV-irradiation is offered.
研究了紫外线(240 - 390nm)剂量为151、1510、3020J/m²诱导人淋巴细胞凋亡过程中DNA结构状态变化、膜Fas受体表达水平、半胱天冬酶 - 3功能活性、Ca²⁺、p53和细胞色素c蛋白浓度以及活性氧(超氧阴离子自由基、羟基自由基、过氧化氢、单线态氧)的情况。已证实,修饰细胞孵育20小时后,紫外线和活性氧会诱导淋巴细胞DNA片段化。结果表明,与未处理细胞相比,淋巴细胞暴露于紫外线和活性氧后1 - 5小时,膜死亡Fas受体表达水平升高。还发现,单线态氧、羟基自由基和过氧化氢产生后4小时,以及细胞以151和1510J/m²剂量紫外线照射后8小时、24小时以及6小时和8小时,淋巴细胞半胱天冬酶 - 3功能活性增强。使用DNA彗星实验方法发现,淋巴细胞以1510和3020J/m剂量紫外线照射以及加入浓度为10⁻⁶mol/l的过氧化氢后15 - 20分钟会出现DNA损伤(单链断裂)(C1型彗星),细胞修饰后6小时达到最大值(C2和C3型彗星)。观察到,淋巴细胞暴露于1510和3020J/m²的过氧化氢和紫外线后6小时,所研究细胞的p53水平升高。还表明,在紫外线照射(1510J/m²)和外源性活性氧产生条件下,淋巴细胞胞质溶胶中较高的钙水平是由于磷酸肌醇信息传递机制成分激活导致Ca²⁺从细胞内储存库释放所致。提出了关于钙水平变化与紫外线照射和活性氧暴露后人淋巴细胞程序性细胞破坏启动之间相关性的观点。作者得出结论,在151和1510J/m²剂量紫外线和活性氧代谢产物诱导淋巴细胞凋亡过程中,受体介导(Fas依赖)的半胱天冬酶和p53依赖途径起主导作用。给出了淋巴细胞紫外线照射后可能导致其凋亡破坏的细胞内事件模式。