Heavy ion radiation induces pyroptosis in skin keratinocytes through a mitogen-activated protein kinase signaling pathway.

IF 2.4
Zhiqiang Zhang, Haoxiang Wang, Yumeng Huang, Liming Zhu, Xuanyu Wang, Yan Du, Guangming Zhou, Ye Zhao
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Abstract

Purpose: To elucidate the mechanisms underlying pyroptosis in skin due to heavy ion radiation.

Materials and methods: Human keratinocytes (HaCaT cells) were irradiated with different doses of X-rays and 12C ions. Clonogenic survival, CCK-8 cell proliferation, and micronucleus assays were performed to assess the radiosensitivity of HaCaT cells. The pyroptosis-related, inflammation-related, and MAPK/NF-κB signaling pathway proteins were detected by Western-blotting.

Results: 12C ion radiation caused more severe damage to HaCaT cells than X-rays. The former induced pyroptosis in the HaCaT cells in a dose-dependent manner. Heavy ion-induced pyroptosis was activated by the Caspase-4/Caspase-5/Gasdermin D (GSDMD) pathway, which was regulated by the MAPK/NF-κB signaling pathway.

Conclusions: 12C ion irradiation induced pyroptosis in human keratinocytes by a non-classical pathway via the activation of MAPK/NF-κB signaling pathway. The findings may be used to guide further research on targeted interventions to reduce skin damage and optimize treatment strategies in the future.

重离子辐射通过丝裂原激活的蛋白激酶信号通路诱导皮肤角质形成细胞焦亡。
目的:探讨重离子辐射致皮肤焦亡的机制。材料和方法:用不同剂量的x射线和12C离子照射人角质形成细胞(HaCaT细胞)。通过克隆性存活、CCK-8细胞增殖和微核试验来评估HaCaT细胞的放射敏感性。Western-blotting检测焦热相关、炎症相关、MAPK/NF-κB信号通路蛋白表达。结果:12C离子辐射对HaCaT细胞的损伤比x射线更严重。前者以剂量依赖的方式诱导HaCaT细胞焦亡。重离子诱导的焦亡通过Caspase-4/Caspase-5/Gasdermin D (GSDMD)通路激活,该通路受MAPK/NF-κB信号通路调控。结论:12C离子辐照可通过激活MAPK/NF-κB信号通路,通过非经典途径诱导人角质形成细胞焦亡。该研究结果可用于指导未来进一步研究有针对性的干预措施,以减少皮肤损伤并优化治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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