Shanghai Key Laboratory for the Prevention and Treatment of Bone and Joint Diseases with Integrated Chinese-Western Medicine, Shanghai Institute of Traumatology and Orthopedics, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine. Address: No. 197, Rui Jin Er Road, Shanghai 200025 China.
Department of Bone Metabolism, Institute of Radiation Medicine, Fudan University, Shanghai 200032, China. Address: No. 2094, Xietu Road, Shanghai 200032 China.
Sci Rep. 2016 Aug 8;6:31318. doi: 10.1038/srep31318.
Radiation therapy is commonly used to treat cancer patients but exhibits adverse effects, including insufficiency fractures and bone loss. Epigenetic regulation plays an important role in osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs). Here, we reported local bone changes after single-dose exposure to (137)CS irradiation in rats. Femur bone mineral density (BMD) and trabecular bone volume in the tibia were significantly decreased at 12 weeks after irradiation. Micro-CT results showed that tBMD, Tb.h and Tb.N were also significantly reduced at 12 weeks after irradiation exposure. ALP-positive OB.S/BS was decreased by 42.3% at 2 weeks after irradiation and was decreased by 50.8% at 12 weeks after exposure. In contrast to the decreased expression of Runx2 and BMP2, we found EZH2 expression was significantly increased at 2 weeks after single-dose (137)CS irradiation in BMSCs. Together, our results demonstrated that single-dose (137)CS irradiation induces BMD loss and the deterioration of bone microarchitecture in the rat skeleton. Furthermore, EZH2 expression increased and osteoblastogenesis decreased after irradiation. The underlying mechanisms warrant further investigation.
放射治疗常用于治疗癌症患者,但会产生不良反应,包括骨强度下降和骨质流失。表观遗传调控在骨髓间充质干细胞(BMSCs)的成骨分化中发挥重要作用。在这里,我们报道了大鼠单次(137)CS 照射后局部骨变化。照射后 12 周,股骨骨密度(BMD)和胫骨小梁骨体积明显降低。微 CT 结果显示,照射后 12 周 tBMD、Tb.h 和 Tb.N 也明显降低。照射后 2 周,ALP 阳性 OB.S/BS 降低了 42.3%,照射后 12 周降低了 50.8%。与 Runx2 和 BMP2 表达降低相反,我们发现 EZH2 表达在单次(137)CS 照射后 2 周的 BMSCs 中显著增加。总之,我们的研究结果表明单次(137)CS 照射导致大鼠骨骼中 BMD 丢失和骨微结构恶化。此外,照射后 EZH2 表达增加,成骨细胞生成减少。其潜在机制值得进一步研究。