Holgersson A, Jernberg A R-M, Persson L M, Edgren M R, Lewensohn R, Nilsson A, Brahme A, Meijer A E
Unit of Medical Radiation Biology, Department of Oncology-Pathology, Cancer Centre Karolinska, Stockholm, Sweden.
Int J Radiat Biol. 2003 Aug;79(8):611-21. doi: 10.1080/09553000310001596995.
To investigate and compare the ability of DNA-dependent protein kinase (DNA-PK)-deficient and -proficient cells to undergo apoptosis after exposure to low and high linear energy transfer (LET) radiation.
A human glioma cell line M059J lacking the catalytic subunit of DNA-PK (DNA-PKcs) and its DNA-PKcs-proficient counterpart, M059K, were exposed to 1 and 4 Gy of accelerated nitrogen ions (14N, 140 eV nm(-1), 8-12 Gy min(-1)) or 60Co gamma-rays (0.2 eV nm(-1), 0.7 Gy min(-1)). The induction of apoptosis was studied up to 144 h post-irradiation using two different methods: morphological characterization of apoptotic cells after fluorescent staining and cell size distribution analysis to detect apoptotic bodies. In parallel, protein expression of DNA-PKcs and poly(ADP-ribose) polymerase (PARP) as well as DNA-PK and caspase-3 activity were investigated.
Low and high LET radiations (4 Gy) induced a time-dependent apoptotic response in both cell lines. Low LET radiation induced a significantly elevated apoptotic response in M059J as compared with M059K cells at 144 h post-irradiation. Following high LET radiation exposure, there was no difference between the cell lines at this time. PARP cleavage was detected in M059J cells following both low and high LET irradiation, while only high LET radiation induced PARP cleavage in M059K cells. These cleavages occurred in the absence of caspase-3 activation.
M059J and M059K cells both display radiation-induced apoptosis, which occur independently of caspase-3 activation. The apoptotic course differs between the two cell lines and is dependent on the quality of radiation.
研究并比较DNA依赖性蛋白激酶(DNA-PK)缺陷型和正常型细胞在受到低、高线性能量传递(LET)辐射后发生凋亡的能力。
将缺乏DNA-PK催化亚基(DNA-PKcs)的人胶质瘤细胞系M059J及其DNA-PKcs正常的对应细胞系M059K,分别暴露于1 Gy和4 Gy的加速氮离子(¹⁴N,140 eV nm⁻¹,8 - 12 Gy min⁻¹)或⁶⁰Coγ射线(0.2 eV nm⁻¹,0.7 Gy min⁻¹)。照射后长达144小时,使用两种不同方法研究凋亡诱导情况:荧光染色后对凋亡细胞进行形态学特征分析以及通过细胞大小分布分析检测凋亡小体。同时,研究DNA-PKcs和聚(ADP-核糖)聚合酶(PARP)的蛋白表达以及DNA-PK和半胱天冬酶-3的活性。
低、高线性能量传递辐射(4 Gy)在两种细胞系中均诱导了时间依赖性的凋亡反应。在照射后144小时,与M059K细胞相比,低LET辐射在M059J细胞中诱导的凋亡反应显著升高。在高线性能量传递辐射暴露后,此时两种细胞系之间没有差异。在低LET和高LET照射后的M059J细胞中均检测到PARP裂解,而仅高LET辐射在M059K细胞中诱导了PARP裂解。这些裂解在没有半胱天冬酶-3激活的情况下发生。
M059J和M059K细胞均表现出辐射诱导的凋亡,且凋亡发生独立于半胱天冬酶-3激活。两种细胞系的凋亡过程不同,且取决于辐射的性质。