Vile G F, Tanew-Ilitschew A, Tyrrell R M
Swiss Institute for Experimental Cancer Research (ISREC), Epalinges.
Photochem Photobiol. 1995 Sep;62(3):463-8. doi: 10.1111/j.1751-1097.1995.tb02369.x.
We have examined the role of the nucleus and the membrane in the activation of nuclear factor (NF)-kappa B by oxidant stress generated via the UVA (320-380 nm) component of solar radiation. Nuclear extracts from human skin fibroblasts that had been irradiated with UVA at doses that caused little DNA damage contained activated NF-kappa B that bound to its recognition sequence in DNA. The UVA radiation-dependent activation of NF-kappa B in enucleated cells confirmed that the nucleus was not involved. On the other hand, UVA radiation-dependent activation of NF-kappa B appeared to be correlated with membrane damage, and activation could be prevented by alpha-tocopherol and butylated hydroxytoluene, agents that inhibited UVA radiation-dependent peroxidation of cell membrane lipids. The activation of NF-kappa B by the DNA damaging agents UVC (200-290 nm) and UVB (290-320 nm) radiation also only occurred at doses where significant membrane damage was induced, and, overall, activation was not correlated with the relative levels of DNA damage induced by UVC/UVB and UVA radiations. We conclude that the oxidative modification of membrane components may be an important factor to consider in the UV radiation-dependent activation of NF-kappa B over all wavelength ranges examined.
我们研究了细胞核和细胞膜在太阳辐射的UVA(320 - 380纳米)成分所产生的氧化应激激活核因子(NF)-κB过程中的作用。用造成少量DNA损伤剂量的UVA照射的人皮肤成纤维细胞核提取物中含有与DNA中其识别序列结合的活化NF-κB。去核细胞中NF-κB的UVA辐射依赖性激活证实细胞核不参与其中。另一方面,NF-κB的UVA辐射依赖性激活似乎与膜损伤相关,并且α-生育酚和丁基化羟基甲苯(抑制细胞膜脂质UVA辐射依赖性过氧化的试剂)可以阻止这种激活。DNA损伤剂UVC(200 - 290纳米)和UVB(290 - 320纳米)辐射激活NF-κB也仅在诱导显著膜损伤的剂量下发生,并且总体而言,激活与UVC/UVB和UVA辐射诱导的DNA损伤相对水平无关。我们得出结论,在所研究的所有波长范围内,膜成分的氧化修饰可能是UV辐射依赖性激活NF-κB时需要考虑的一个重要因素。