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首页> 外文期刊>Oncogene >Ultraviolet irradiation-induced K|[plus]| channel activity involving p53 activation in corneal epithelial cells
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Ultraviolet irradiation-induced K|[plus]| channel activity involving p53 activation in corneal epithelial cells

机译:紫外线诱导的K | [plus ||角膜上皮细胞中涉及p53激活的通道活性

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Recent studies from our lab found that ultraviolet (UV) irradiation induces a voltage-gated potassium (Kv) channel activation and subsequently activates JNK signaling pathway resulting in apoptosis. The present study in rabbit corneal epithelial (RCE) cells is to investigate mechanisms of UV irradiation-induced Kv channel activity involving p53 activation in parallel to DNA damage-induced signaling pathway. UV irradiation-induced signaling events were characterized by measurements of JNK activation and further downstream p53 phosphorylation. UV irradiation elicited an early response in the cell membrane through activation of Kv channels to activate the JNK signaling pathway and p53 phosphorylation. Exposure of RCE cells to UV irradiation within a few min resulted in JNK and p53 activations that were markedly inhibited by suppression of Kv channel activity. However, suppression of Kv channel activity failed to prevent p53 activation induced by extended DNA damages through prolonging UV exposure time (more than 15min). In addition, caffeine inhibited UV-induced activation of SEK, an upstream MAPK kinase of JNK, resulting in suppression of both Kv channel-involved and DNA damage-induced p53 activation. Our results indicate in these cells that UV irradiation induces earlier and later intracellular events that link to activation of JNK and p53. The early event in response to UV irradiation is initiated by activating Kv channels in the cell membrane, and the later event is predominated by UV irradiation-caused DNA damage.
机译:我们实验室的最新研究发现,紫外线(UV)辐射可诱导电压门控钾(Kv)通道激活,并随后激活JNK信号传导途径,从而导致细胞凋亡。目前在兔角膜上皮(RCE)细胞中的研究是调查机制的紫外线照射诱导的Kv通道活性涉及p53激活平行于DNA损伤诱导的信号通路。 UV辐射诱导的信号转导事件通过JNK激活和进一步下游p53磷酸化的测量来表征。紫外线照射通过激活Kv通道激活JNK信号通路和p53磷酸化引起细胞膜的早期反应。 RCE细胞在几分钟内暴露于紫外线照射下会导致JNK和p53激活,而这些激活明显受到Kv通道活性抑制的抑制。但是,Kv通道活性的抑制不能通过延长紫外线暴露时间(超过15分钟)来阻止由延长的DNA损伤诱导的p53活化。此外,咖啡因抑制了UV诱导的SEK(JNK的上游MAPK激酶)的激活,从而抑制了Kv通道参与和DNA损伤诱导的p53激活。我们的结果表明,在这些细胞中,紫外线辐射诱导了与JNK和p53激活相关的早期和晚期细胞内事件。响应紫外线辐射的早期事件是通过激活细胞膜中的Kv通道引发的,而后来的事件则主要是由于紫外线辐照引起的DNA损伤。

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