癌变·畸变·突变 ›› 2026, Vol. 38 ›› Issue (2): 108-112,118.doi: 10.3969/j.issn.1004-616x.2026.02.004

• 论著 • 上一篇    

放射性皮肤损伤中细胞干性的转变

关子易, 余南希, 程雪艳, 马丽萍, 高玲   

  1. 中国疾病预防控制中心辐射防护与核安全医学所, 辐射防护与核应急中国疾病预防控制中心重点实验室, 北京 100088
  • 收稿日期:2025-08-20 修回日期:2025-10-16 发布日期:2026-04-09
  • 通讯作者: 高玲
  • 作者简介:关子易,E-mail:guan_ziyi@hotmail.com。

Cellular stemness transition in radiation-induced skin injury in vitro and in vivo

GUAN Ziyi, YU Nanxi, CHENG Xueyan, MA Liping, GAO Ling   

  1. Key Laboratory of Radiological Protection and Nuclear Emergency, National Institute for Radiological Protection, Chinese Center for Disease Control and Prevention, Beijing 100088, China
  • Received:2025-08-20 Revised:2025-10-16 Published:2026-04-09

摘要: 目的: 研究放射性皮肤损伤中细胞干性的变化。方法: 体外细胞试验中,分别采用0、5、10和20 Gy组X射线对人永生化角质形成细胞HaCaT进行一次性照射,通过细胞划痕法、Transwell法检测照射后24和48 h细胞的迁移能力,用Western blot法检测HaCaT细胞照射后24和48 h干性相关蛋白KLF4、c-myc和LGR5的表达。在动物试验中,对SD大鼠右后肢皮肤进行20 Gy X射线照射,在照后第15和35天用Western blot法检测照射部位皮肤细胞中干性相关SOX2、Nanog、KLF4、c-myc、LGR5蛋白的表达,同时设未照射对照组(0 Gy),每组4只大鼠。结果: 在体外细胞试验中,与对照组(0 Gy)相比,照射48 h后,细胞划痕法显示5、10和20 Gy X射线照射后细胞迁移能力均明显降低(P<0.05),而Transwell实验结果显示细胞的迁移能力显著增强(P<0.01),10 Gy时仍保持一定迁移能力;在照射后24 h,不同剂量照射组HaCaT细胞中KLF4、c-myc和LGR5蛋白表达水平均显著降低(P<0.01),而在照射后48 h,KLF4、c-myc和LGR5蛋白表达水平均显著升高(P<0.01)。在动物试验中,与对照组(0 Gy)相比,20 Gy X射线照射大鼠皮肤第15天后,干性相关SOX2、c-myc和LGR5蛋白表达水平升高(均为P<0.01);照射第35天后SOX2、Nanog、LGR5蛋白表达水平显著降低(P<0.05或P<0.01)。结论: 在放射性皮肤损伤中,细胞干性转变能力是动态变化的,早期可能抑制修复,中期可能促进再生,但长期干性转变能力可能逐渐降低。

关键词: 电离辐射, 皮肤损伤, 干性基因, 修复

Abstract: OBJECTIVE: To investigate changes in cellular stemness transition in radiation-induced skin injury in cell culture. METHODS: Human immortalized keratinocytes(Ha Ca T) were exposed to X-ray at 0,5,10,and 20 Gy. Cell migration ability at 24 h and 48 h post-irradiation was assessed using the scratch wound healing assay and transwell migration assay. Western blot was used to detect the expression of stemness-related proteins KLF4,c-myc and LGR5 in Ha Ca T cells at 24 h and 48 h after irradiation. In the animal experiments,the skin of the right hind limb of SD rats was irradiated with a single dose of 20 Gy X-ray. At 15 and 35 days post-irradiation, western blot was performed to detect the expression of stemness-related proteins SOX2,Nanog, KLF4, c-myc, and LGR5 in the irradiated skin cells. A non-irradiated control group(0 Gy) was included, with 4 rats per group. RESULTS: Compared with the control group(0 Gy), the in vitro scratch wound healing assay at 48 h post-irradiation showed that cell migration ability was significantly reduced in the5, 10, and 20 Gy groups(P<0.05). In contrast, the transwell assay demonstrated significantly enhanced migration ability in all irradiated groups(P<0.01), with the 10 Gy group still retaining a certain level of migration capacity. At 24 h post-irradiation,KLF4,c-myc and LGR5 protein expression levels in Ha Ca T cells were significantly decreased in all irradiated dose groups(P<0.01). At 48 h post-irradiation,KLF4,c-myc and LGR5 protein expression levels were significantly increased(P<0.01). In the animal experiments,compared with the control group(0 Gy), at 15 days after 20 Gy X-ray irradiation, expression levels of stemness-related proteins SOX2, c-Myc, and LGR5 in rat skin were significantly elevated(all P<0.01). At 35 days postirradiation, expression levels of SOX2, Nanog, and LGR5 were significantly decreased(P<0.05 or P<0.01).CONCLUSION: In radiation-induced skin injury, cellular stemness transition capacity expressed dynamic changes which might cause inhibition of repair,promotion of regeneration with gradual decline in the long term.

Key words: ionizing radiation, skin injury, stemness genes, repair

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