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[0.5吉电子伏特X射线辐射通过Wnt/β-连环蛋白信号通路促进成骨细胞分化]

[0.5 Gy X-ray radiation promotes osteoblast differentiation by Wnt/β-Catenin signaling].

作者信息

Chen M, Dong Q R, Huang Q, She C, Xu W

机构信息

Department of Orthopedics, the Second Hospital Affiliated to Soochow University, Suzhou 215004, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2017 Jun 20;97(23):1820-1825. doi: 10.3760/cma.j.issn.0376-2491.2017.23.013.

Abstract

To investigate the important roles of Wnt signaling in the processes of 0.5Gy X-ray promoting osteoblast differentiation, and make clear the molecular mechanisms involved. Flow cytometry was employed to detect the apoptosis after osteoblast exposure to 0.5 Gy X-ray radiation.The protein level of osteoblast differentiation markers, such as collagen Iα (Col1α), alkaline phosphatase (ALP), osteocalcin (OCN), were detected by Western-blot and ALP activity staining was performed. Real-time PCR and Western-blot were utilized to evaluate the variations of key factors in Wnt signaling pathways, while specific inhibitor of Wnt/β-Catenin, XAV939 was used to block the Wnt signaling. Low-dose (0.5 Gy) X-ray induced significant decline in MC3T3-E1 osteoblast apoptosis at three days after radiation.The dynamic variations in the expression of osteoblast differentiation markers, including Col1α, ALP, OCN, were observed after 0.5 Gy X-ray irradiation by Western blot analysis.The protein levels of Col1α have a reduction temporarily at 4 days of radiation (34.5%±5.8%, =9.912, <0.001), then a significant increase is detected at 10 day after radiation (162.5%±6.5%, =2.673, <0.05). OCN levels dropped by 83% (=3.968, <0.01) at 4 day after 0.5 Gy X-ray radiation, and raised at 10 day (39.5%±4.1%, =3.219, <0.05) and 14 day (79.4%±7.5%, =6.708, <0.001), respectively. ALP levels increased at 7 day (79.7%±22.3%, =6.257, <0.001) and 10 day(128.3%±6.1%, =4.340, <0.01)after radiation. At the same time, 0.5 Gy X-ray radiation can activate Wnt/GSK-3/β-Catenin signaling.The mRNA levels of Wnt3a、LPR5 and TCF-4 increased by 1.7 fold (=6.573, <0.001), 1.1 fold (=5.323, <0.05) and 1.4 fold (=3.054, <0.05) at 7 day after radiation.In addition, p-GSK-3β level reduced by 42.1% (=4.460, <0.01), and active β-Catenin increased by 1.9 fold (=3.528, <0.05). However, the specific inhibitor of Wnt/β-Catenin, XAV939 completely abrogated Wnt/β-Catenin signaling and the increase in ALP expression and activity induced by 0.5 Gy X-ray radiation. These results demonstrated that low dose X-ray radiation promoted osteoblast survival at early differentiation, and promoted differentiation at middle and late stage, in which Wnt signaling participated the regulation processes.

摘要

为研究Wnt信号通路在0.5Gy X射线促进成骨细胞分化过程中的重要作用,并明确其涉及的分子机制。采用流式细胞术检测成骨细胞暴露于0.5Gy X射线辐射后的凋亡情况。通过蛋白质免疫印迹法检测成骨细胞分化标志物如I型胶原蛋白α1(Col1α)、碱性磷酸酶(ALP)、骨钙素(OCN)的蛋白水平,并进行ALP活性染色。利用实时荧光定量PCR和蛋白质免疫印迹法评估Wnt信号通路关键因子的变化,同时使用Wnt/β-连环蛋白特异性抑制剂XAV939阻断Wnt信号通路。低剂量(0.5Gy)X射线照射后3天,MC3T3-E1成骨细胞凋亡显著下降。通过蛋白质免疫印迹分析观察到0.5Gy X射线照射后成骨细胞分化标志物Col1α、ALP、OCN表达的动态变化。Col1α蛋白水平在照射后4天暂时降低(34.5%±5.8%,t = 9.912,P < 0.001),随后在照射后10天显著升高(162.5%±6.5%,t = 2.673,P < 0.05)。0.5Gy X射线辐射后4天,OCN水平下降83%(t = 3.968,P < 0.01),并在10天(39.5%±4.1%,t = 3.219,P < 0.05)和14天(79.4%±7.5%,t = 6.708,P < 0.001)升高。照射后7天(79.7%±22.3%,t = 6.257,P < 0.001)和10天(128.3%±6.1%,t = 4.340,P < 0.01)ALP水平升高。同时,0.5Gy X射线辐射可激活Wnt/GSK-3/β-连环蛋白信号通路。照射后7天,Wnt3a、LPR5和TCF-4的mRNA水平分别升高1.7倍(t = 6.573,P < 0.001)、1.1倍(t = 5.323,P < 0.05)和1.4倍(t = 3.054,P < 0.05)。此外,p-GSK-3β水平降低42.1%(t = 4.460,P < 0.01),活性β-连环蛋白增加1.9倍(t = 3.528,P < 0.05)。然而,Wnt/β-连环蛋白特异性抑制剂XAV939完全消除了Wnt/β-连环蛋白信号通路以及0.5Gy X射线辐射诱导的ALP表达和活性增加。这些结果表明,低剂量X射线辐射促进成骨细胞早期分化阶段的存活,并在中晚期促进分化,其中Wnt信号通路参与了调控过程。

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