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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Khellin, but not 8-methoxypsoralen, inhibits adenylyl cyclase system in HeLa cells
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Khellin, but not 8-methoxypsoralen, inhibits adenylyl cyclase system in HeLa cells

机译:Khellin,但不是8-甲氧基甲苯,抑制了HeLa细胞中的腺苷酸环酶系统

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摘要

Until recently, the therapeutic effects of furocoumarins and furochromones plus UV-A light were thought to be due to their ability to form photoadducts with DNA in the cell nuclei; now it appears that membrane effector systems may be involved as targets. Here we show that in HeLa cells khellin at 1 and 5 μM final concentration, in combination with UV-A light, inhibits NaF-stimulated adenylyl cyclase activity and Pertussis Toxin (PT)-catalyzed ADP-ribosylation of α-subunits of inhibitory guanine nucleotide regulatory proteins (Gi) and increases GTPase activity. In the same experimental conditions, 8-methoxypsoralen (8-MOP), either alone or plus UV-A, does not affect adenylyl cyclase and GTPase activities. Our results suggest that in HeLa cells, through an interaction with a receptor and the mediation of Gi proteins, the adenylyl cyclase system is a target for khellin but not for 8-MOP.
机译:直到最近,呋喃马辛和Furochromones加上紫外线的治疗效果是由于它们能够在细胞核中与DNA形成光化的能力; 现在似乎膜效应系统可以作为目标涉及。 在这里,我们表明,在HeLa细胞Khellin的1和5μm最终浓度中,与UV-A光相结合,抑制NAF刺激的腺苷酸环化酶活性和百日咳毒素(PT) - 催化瘤核蝶核苷酸的α-亚基的α-亚基化 调节蛋白(GI)并增加GTP酶活性。 在相同的实验条件下,单独或加上UV-A的8-甲氧基甲醛(8-MOP)不影响腺苷酸环化酶和GTP酶活性。 我们的研究结果表明,在HeLa细胞中,通过与受体的相互作用和Gi蛋白的调解,腺苷环化酶系统是Khellin但不适用于8-MOP的靶标。

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