DONG Xiao-rong,DONG Ji-hua,ZHANG Rui-guang,FAN Li,LIU Li,ZHANG Tao,WU Gang.Inhibitory effects of Tanshinone Ⅱ A on radiation-induced inflammatory response in microglia BV-2 cells[J].Chinese Journal of Radiological Medicine and Protection,2010,30(5):535-539
Inhibitory effects of Tanshinone Ⅱ A on radiation-induced inflammatory response in microglia BV-2 cells
Received:November 24, 2009  
DOI:
KeyWords:Irradiation  DNA double-strand break  Microglia cells  Inflammatory response  Tanshinone ⅡA
FundProject:国家自然科学基金(30800283)
Author NameAffiliationE-mail
DONG Xiao-rong Cancer Center, Union Hospital, Huazhong University of Science and Technology, Wuhan 430022, China  
DONG Ji-hua 华中科技大学同济医学院附属协和医院肿瘤研究中心, 中心实验室  
ZHANG Rui-guang Cancer Center, Union Hospital, Huazhong University of Science and Technology, Wuhan 430022, China  
FAN Li Cancer Center, Union Hospital, Huazhong University of Science and Technology, Wuhan 430022, China  
LIU Li Cancer Center, Union Hospital, Huazhong University of Science and Technology, Wuhan 430022, China  
ZHANG Tao Cancer Center, Union Hospital, Huazhong University of Science and Technology, Wuhan 430022, China  
WU Gang Cancer Center, Union Hospital, Huazhong University of Science and Technology, Wuhan 430022, China hustxiehe@hotmail.com 
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Abstract::
      Objective To explore the inhibitory effects of Tanshinone ⅡA on the radiation-induced microglia activation and the possible mechanism. Methods Microglia cells BV-2 were irradiated with 2, 4, 8, 16, and 32 Gy doses or sham-irradiated in presence or absence of 1.0 μg/ml Tanshinone ⅡA for 12 h,respectively. The effects of Tanshinone ⅡA on radiation-induced pro-inflammatory cytokines were evaluated using real-time PCR. The expression level of NF-κB p65 in cytoplasm and nucleus was measured by using Western blot. Immunofluorescence staining and confocal microscopy analysis were applied to detect the expression of γ-H2AX and p65 post-irradiation. Results The microglia cells were activated at 16, 32 Gy post-irradiation. Radiation-induced release of the pro-inflammatory cytokines in BV-2 cells was detectable after irradiation. Tanshinone ⅡA decreased radiation-induced release of pro-inflammatory cytokines(t=5.56, P<0.05). Furthermore, western blotting showed that Tanshinone ⅡA could attenuate the nuclear translocation of NF-κB p65 submit post-irradiation. Immunofluorescence staining showed that γ-H2AX foci formation while p65 translocation into nucleus post-irradiation. Conclusions Tanshinone ⅡA exerts anti-inflammatory properties by suppressing the transcription of pro-inflammatory cytokine genes that might be associated with NF-κB signaling pathway. It is postulated that irradiation causes immediate cellular reaction and DSB triggers the molecular response which leads to NF-κB pathway activation.
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