Jin Jie, Wang Yu, Wang Jin, Xu Yang, Chen Shilei, Wang Junping, Ran Xinze, Su Yongping
Institute of Combined Injury, State Key Laboratory of Trauma, Burns and Combined Injury, Chongqing Engineering Research Center for Nanomedicine, College of Preventive Medicine, Third Military Medical University, Chongqing 400038, China.
J Radiat Res. 2014 May;55(3):443-50. doi: 10.1093/jrr/rrt132. Epub 2013 Dec 5.
Steroid receptor coactivator-3 (SRC-3), a multifunctional transcriptional coactivator, plays an important role in regulation of cell apoptosis in chemoresistant cancer cells. However, its role in radiation-induced apoptosis in hematopoietic cells is still unclear. In this study, we used SRC-3 knockout (SRC-3(-/-)) mice to assess the role of SRC-3 in radiation-induced hematopoietic injury in vivo. After a range of doses of irradiation, SRC-3(-/-) mice exhibited lower counts of peripheral blood cells and bone marrow (BM) mononuclear cells and excessive BM depression, which resulted in a significantly higher mortality compared with wildtype mice. Moreover, BM mononuclear cells obtained from SRC-3(-/-) mice showed a remarkable increase in radiation-induced apoptosis. Collectively, our data demonstrate that SRC-3 plays a role in radiation-induced apoptosis of BM hematopoietic cells. Regulation of SRC-3 might influence the radiosensitivity of hematopoietic cells, which highlights a potential therapeutic target for radiation-induced hematopoietic injury.
类固醇受体辅激活因子-3(SRC-3)是一种多功能转录辅激活因子,在化疗耐药癌细胞的细胞凋亡调控中发挥重要作用。然而,其在造血细胞辐射诱导凋亡中的作用仍不清楚。在本研究中,我们使用SRC-3基因敲除(SRC-3(-/-))小鼠来评估SRC-3在体内辐射诱导造血损伤中的作用。在一系列剂量的照射后,SRC-3(-/-)小鼠外周血细胞和骨髓(BM)单个核细胞计数较低,且骨髓抑制过度,与野生型小鼠相比,其死亡率显著更高。此外,从SRC-3(-/-)小鼠获得的BM单个核细胞在辐射诱导的凋亡方面显著增加。总体而言,我们的数据表明SRC-3在BM造血细胞辐射诱导的凋亡中起作用。对SRC-3的调控可能会影响造血细胞的放射敏感性,这突出了辐射诱导造血损伤的一个潜在治疗靶点。