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外周血淋巴细胞对γ射线照射反应中组蛋白H2A.X和p53磷酸化的变化。

Changes in phosphorylation of histone H2A.X and p53 in response of peripheral blood lymphocytes to gamma irradiation.

作者信息

Vilasová Zdenka, Rezácová Martina, Vávrová Jirina, Tichý Ales, Vokurková Doris, Zoelzer Friedo, Reháková Zuzana, Osterreicher Jan, Lukásová Emilie

机构信息

University of Defence, Faculty of Military Health Sciences, Department of Radiobiology, Hradec Králové, Czech Republic.

出版信息

Acta Biochim Pol. 2008;55(2):381-90.

Abstract

The main aim of this study was to compare the reaction of quiescent and proliferating, i.e. phytohemagglutinin (PHA)-stimulated, human peripheral blood mononuclear cells (PBMCs) to gamma-radiation, and analyse changes of proteins related to repair of DNA damage and apoptosis, such as gammaH2A.X, p53, p53 phosphorylation at serines-15 and -392, and p21 and their dose dependence. Freshly isolated PBMCs in peripheral blood are predominantly quiescent, in G(0) phase, and with very low amounts of proteins p53 and p21. Using confocal microscopy we detected dose dependent (0.5-5 Gy) induction of foci containing gammaH2A.X (1 h after gamma-ray exposure), which are formed around radiation-induced double strand breaks of DNA. Apoptosis was detected from 24 h after irradiation by the dose of 4 Gy onwards by Annexin V binding and lamin B cleavage. Seventy two hours after irradiation 70% of CD3(+) lymphocytes were A(+). Neither increase in p53 nor its phosphorylation on serine-392 after irradiation was detected in these cells. However, massive increase in p21 (cyclin-dependent kinase inhibitor 1A) was detected after irradiation, which can be responsible for late occurrence of apoptosis in these quiescent cells. PHA-stimulation itself (72 h) caused an increase in early apoptosis (A(+)PI(-)) in comparison to non-stimulated PBMCs (38% A(+) resp. 13.4%). After PHA-stimulation also the amount of gammaH2A.X, p53, and p21 increased, but no phosphorylation of p53 on serine-392 or -15 was detected. Reaction to gamma-radiation was different in PHA-stimulated lymphocytes: the p53 pathway was activated and p53 was phosphorylated on serines-15 and -392 4 h after irradiation by the dose of 4 Gy. Phosphorylation of p53 at serine-15 increased in a dose-dependent manner in the studied dose range 0.2-7.5 Gy. Also the amount of p21 increased after irradiation. Seventy two hours after irradiation of PHA-stimulated CD3(+) T lymphocytes by the dose of 4 Gy 65% of cells were A(+).

摘要

本研究的主要目的是比较静止和增殖状态(即经植物血凝素(PHA)刺激)的人外周血单个核细胞(PBMC)对γ辐射的反应,并分析与DNA损伤修复和细胞凋亡相关的蛋白质变化,如γH2A.X、p53、丝氨酸15和392处的p53磷酸化以及p21及其剂量依赖性。外周血中新鲜分离的PBMC主要处于静止状态,处于G(0)期,p53和p21蛋白含量极低。利用共聚焦显微镜,我们检测到含γH2A.X的病灶的剂量依赖性(0.5 - 5 Gy)诱导(γ射线照射后1小时),这些病灶在辐射诱导的DNA双链断裂周围形成。通过Annexin V结合和核纤层蛋白B裂解,从照射剂量为4 Gy后24小时开始检测到细胞凋亡。照射72小时后,70%的CD3(+)淋巴细胞呈凋亡阳性(A(+))。在这些细胞中未检测到照射后p53及其丝氨酸392处磷酸化的增加。然而,照射后检测到p21(细胞周期蛋白依赖性激酶抑制剂1A)大量增加,这可能是这些静止细胞中晚期细胞凋亡发生的原因。与未刺激的PBMC相比,PHA刺激本身(72小时)导致早期细胞凋亡(A(+)PI(-))增加(分别为38% A(+)和13.4%)。PHA刺激后,γH2A.X、p53和p21的量也增加,但未检测到p53在丝氨酸392或15处的磷酸化。PHA刺激的淋巴细胞对γ辐射的反应不同:p53途径被激活,在照射剂量为4 Gy后4小时,p53在丝氨酸15和392处被磷酸化。在0.2 - 7.5 Gy的研究剂量范围内,p53丝氨酸15处的磷酸化呈剂量依赖性增加。照射后p21的量也增加。照射剂量为4 Gy的PHA刺激的CD3(+) T淋巴细胞72小时后,65%的细胞呈凋亡阳性(A(+))。

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