XU Weiqiang, TANG Geng, LIU Chunyan, LI Xin, YANG Yanming, GONG Shouliang, YU Lei, WANG Zhicheng
Objective To explore the effects of radiation on proliferation and DNA damage repair, and to clarify the relationship between them.Methods Lentivirus plasmids of shATRX1, shATRX2 and shATRX3 were transfected into 293T cells, H460 cells were infected by lentivirus, shATRX1-H460, shATRX2-H460 and shATRX3-H460 cell lines with low/no ATRX expression were obtained, shControl-H460 cells was used as the control. The silencing efficiency was detected by Western blot. Cell proliferation was measured by colony formation assay, γH2AX and Rad51 foci were detected by immunofluorescence, and the numbers were counted, PARP1, γH2AX and Rad51 expressions were measured by Western blot, respectively.Results ATRX expressed in H460 and shControl-H460 cells, while reduced in shATRX1-H460, shATRX2-H460 and shATRX3-H460 cells. The colony formation assay showed that the SFs of shATRX2-H460 and shATRX3-H460 cells was lower than that of shControl-H460 cells. After shControl-H460 and shATRX3-H460 cells were irradiated by 4 Gy at 1 h, γH2AX foci reached a maximum, while Rad51 foci reached a maximum, at 3 h, and then decreased. Compared with shControl-H460 cells, γH2AX foci at 1 and 6 h, Rad51 foci at 1, 3 and 6 h were significantly increased (P<0.05, P<0.001). And PARP1, γH2AX and Rad51 protein expressions in shATRX3-H460 cells increased at 3 and 6 h compared with that in shContral-H460 cells.Conclusion The cell models of targeted silencing of ATRX in H460 cells were successfully obtained, and the cell proliferation ability was reduced after radiation, which may be related to the reduction of DNA damage repair ability.