RADIATION PROTECTION ›› 2014, Vol. 34 ›› Issue (3): 168-171.

Previous Articles     Next Articles

Apoptosis in HaCaT and Bad Pathways

Xue Zhenan1, Huang Xin2, Cao Di1, Chen Jin1, Huang Kun1, Chen Aijun1   

  1. 1. Department of Dermatology, The first affiliated hospital of Chongqing Medical School, Chongqing 400016;
    2. Institue of traditional Chinese medicine prescription teaching and research center, The first affiliated hospital of Chongqing Medical School, Chongqing 400016
  • Received:2013-12-31 Online:2014-05-20 Published:2025-01-24

Abstract: To study the mechanism of low-doses of ultraviolet B (UVB, 280—315 nm) on human immortalized cells (HaCaT cells) apoptosis, proliferation and Bad pathway, chose the most suitable 5 mJ/cm2 intensity of UVB from 3,5 and 7 mJ/cm2 to irradiate the HaCaT cells for 18, 36 and 72 hours, then, collected the cells for the detection of apoptosis and proliferation; The total protein in HaCaT cells was extracted from the irradiated cell for western blot to detect the expression of AKT, Bad and the Bad-p136. The results showed that the apoptotic effects of 5 mJ/cm2 intensity irradiation on HaCaT cells have no distinguish difference among different time point. But the proliferation rate after 72 hours irradiation on HaCaT cells was significant higher than control group. Immunoblotting experiments confirmed the expression levels of AKT and Bad-p136 were significant increasing compared to normal expression of Bad protein after UVB irradiation. Therefore, a long time UVB radiation of 5 mJ/cm2 may promote cell proliferation signaling pathway by Bad, which may be a potential risk factor for the development of skin tumors.

Key words: cell apoptosis, cell proliferation, ultraviolet UVB

CLC Number: 

  • Q68