Carcinogenesis, Teratogenesis & Mutagenesis ›› 2016, Vol. 28 ›› Issue (5): 364-368.doi: 10.3969/j.issn.1004-616x.2016.05.006

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UVA ultraviolet radiation on cellular injury to human keratinocytes

LI Chen, QI Xuesong, LI Ning, FAN Li, GOU Qiao, LIU Jianxiang, TIAN Mei   

  1. National Institute for Radiological Protection, Key Laboratory of Radiological Protection and Nuclear Emergency, Chinese Center for Disease Control and Prevention, Beijing 100088, China
  • Received:2016-02-04 Revised:2016-04-06 Online:2016-09-30 Published:2016-09-30

Abstract: OBJECTIVE: To investigate the mechanisms and effect of ultra violet A (UVA) radiation on vitality and apoptosis of human keratinocytes (HaCaT). METHODS: After different doses of UVA irradiation to keratinocytes, MTT and flow cytometric analysis were used to detect cell survival and apoptosis;immunofluorescence and Western blot were used to detect the formation of intracellular γH2AX focus and its protein levels;and atomic force microscopy was used to detect DNA breakage. RESULTS: UVA irradiation inhibited survival of HaCaT cells in a dose-response manner at the range of 5-30 J/cm2 (r=0.982,P=0.009). Early apoptotic cell fraction increased significantly at 20th hour after UVA irradiation,and had an increasing trend at the range of 10-40 J/cm2 (r=0.936,P=0.008) with the rising radiation doses. The 30 and 40 J/cm2 doses of UVA induced γH2AX foci formation. After different doses of irradiation,γH2AX expression could be observed,moreover,the expression of γH2AX reached the highest level at 5 J/cm2 and 10 J/cm2 doses. DNA breaks increased significantly over the control group after irradiation,as detected by atomic force microscopy. CONCLUSION: UVA exposure inhibited HaCaT cell survival,promoted its apoptosis and induced DNA chain break,leading to cell death.

Key words: ultra violet A, γH2AX, DNA damage, HaCaT cells

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