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Protecting Intestinal Epithelial Cell Number 6 against Fission Neutron Irradiation through NF-κB Signaling Pathway

机译:通过NF-κB信号通路保护6号肠道上皮细胞免受裂变中子辐照

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摘要

The purpose of this paper is to explore the change of NF-κB signaling pathway in intestinal epithelial cell induced by fission neutron irradiation and the influence of the PI3K/Akt pathway inhibitor . Three groups of IEC-6 cell lines were given: control group, neutron irradiation of 4Gy group, and neutron irradiation of 4Gy with treatment group. Except the control group, the other groups were irradiated by neutron of 4Gy. was given before 24 hours of neutron irradiation. At 6 h and 24 h after neutron irradiation, the morphologic changes, proliferation ability, apoptosis, and necrosis rates of the IEC-6 cell lines were assayed and the changes of NF-κB and PI3K/Akt pathway were detected. At 6 h and 24 h after neutron irradiation of 4Gy, the proliferation ability of the IEC-6 cells decreased and lots of apoptotic and necrotic cells were found. The injuries in treatment and neutron irradiation group were more serious than those in control and neutron irradiation groups. The results suggest that IEC-6 cells were obviously damaged and induced serious apoptosis and necrosis by neutron irradiation of 4Gy; the NF-κB signaling pathway in IEC-6 was activated by neutron irradiation which could protect IEC-6 against injury by neutron irradiation; could inhibit the activity of IEC-6 cells.
机译:本文旨在探讨裂变中子辐照诱导肠上皮细胞NF-κB信号通路的变化及PI3K / Akt通路抑制剂的影响。分为三组IEC-6细胞系:对照组,4Gy中子辐照组和治疗组4Gy中子辐照。除对照组外,其余各组均用4Gy中子辐照。在中子照射24小时之前给予。在中子照射后6 h和24 h,检测IEC-6细胞株的形态变化,增殖能力,凋亡和坏死率,并检测NF-κB和PI3K / Akt途径的变化。中子辐照4Gy后6 h和24 h,IEC-6细胞的增殖能力下降,并发现大量凋亡和坏死细胞。治疗和中子辐照组的伤害比对照组和中子辐照组更严重。结果表明,中子辐照4Gy可明显破坏IEC-6细胞,引起严重的细胞凋亡和坏死。中子辐照激活IEC-6中的NF-κB信号通路,可以保护IEC-6免受中子辐照的伤害。可以抑制IEC-6细胞的活性。

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