首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Adaptive response and the influence of ageing: effects of low-dose irradiation on cell growth of cultured glial cells.
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Adaptive response and the influence of ageing: effects of low-dose irradiation on cell growth of cultured glial cells.

机译:适应性反应和衰老的影响:低剂量照射对培养的神经胶质细胞生长的影响。

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摘要

PURPOSE: To examine the molecular mechanism of radiation adaptive response (RAR) for the growth of cultured glial cells and to investigate the influence of ageing on the response. MATERIALS AND METHODS: Glial cells were cultured from young and older rats (1 and 24 months). RAR for the growth of glial cells conditioned with a low dose of X-rays and subsequently exposed to a high dose of X-rays was examined for cell number and BrdU incorporation. Involvement of the subcellular signalling pathway factors in RAR was investigated using their inhibitors, activators, and mutated and knockout glial cells. RESULTS: RAR was observed in cells cultured from young rats but was not in cells from older animals. The inhibitors of protein kinase C (PKC) and DNA-dependent protein kinase (DNA-PK) or phosphatidylinositol 3-kinase (PI3K) suppressed RAR. The activators of PKC instead of low-dose irradiation also caused RAR. Moreover, glial cells cultured from severe combined immunodeficiency (scid) mice (CB-17 scid) and ataxia-telangiectasia mutated (Atm) knockout mice showed no RAR. CONCLUSION: The results indicated that PKC, ATM, DNAPK and/or PI3K were involved in RAR for growth and BrdU incorporation of cultured glial cells and RAR decreased with ageing.
机译:目的:研究辐射适应性反应(RAR)对培养的神经胶质细胞生长的分子机制,并研究衰老对反应的影响。材料与方法:从幼年和老年大鼠(1和24个月)培养神经胶质细胞。检查了低剂量X射线条件下并随后暴露于高剂量X射线条件下的神经胶质细胞生长的RAR的细胞数量和BrdU掺入。使用其抑制剂,激活剂以及突变和敲除的胶质细胞研究了RAR中亚细胞信号通路因子的参与。结果:在幼鼠培养的细胞中观察到RAR,但在大龄动物的细胞中未观察到RAR。蛋白激酶C(PKC)和DNA依赖性蛋白激酶(DNA-PK)或磷脂酰肌醇3-激酶(PI3K)的抑制剂可抑制RAR。 PKC的活化剂而不是低剂量照射也引起RAR。此外,从严重的联合免疫缺陷(scid)小鼠(CB-17 scid)和共济失调-毛细血管扩张突变(Atm)基因敲除小鼠培养的神经胶质细胞未显示RAR。结论:结果表明PKC,ATM,DNAPK和/或PI3K参与RAR的生长,而培养的神经胶质细胞的BrdU掺入和RAR则随着年龄的增长而降低。

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