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作 者:陈明[1,2] 梁星[3] 温颖[1] 白保晶[1] 黄梦鹿[1] 高卫民[1]
机构地区:[1]首都医科大学附属北京口腔医院修复科,北京100050 [2]口腔生物医学工程教育部重点实验室,四川大学 [3]四川大学华西口腔医院修复科,四川成都610041
出 处:《华西口腔医学杂志》2007年第4期412-414,共3页West China Journal of Stomatology
基 金:国家自然科学基金资助项目(30271428和30672345)
摘 要:目的研究流体切应力对培养于载玻片上的破骨细胞内Ca2+浓度的影响。方法应用激光扫描共聚焦显微镜和Fluo-3/AM荧光探针标记技术,测定加力前后破骨细胞内游离Ca2+的荧光强度,获得的图像在计算机上用图像分析软件进行比较分析。结果在37℃、Fluo-3/AM终浓度为10μmol/L的条件下,破骨细胞可获得良好的标记效果,与未加力的对照组相比,流体切应力使破骨细胞内Ca2+荧光信号的平均强度值显著增加。结论体外培养于载玻片上的破骨细胞内Ca2+浓度对流体切应力敏感,Ca2+可介导流体切应力对破骨细胞功能的调节。Objective To study the change of Ca^2+ density in cultured osteoclast-like ceils in response to fluid shear stress. Methods Laser scanning confocal microscope and fluorescent probe were used to detect the free Ca^2+ in osteoclast-like ceils before and after undergoing fluid shear stress. The images were analyzed and compared with image software. Results At 37 ℃ he free Ca^2+ in osteoclast-like ceils could be labelled effectively with 10 μmol/L Fluo-3/AM. Compared with contol group, the average intensity of Ca^2+ fluorescent signal in osteoclast-like ceils undergoing fluid shear stress increased significantly. Conclusion The Ca^2+ concentration in bone-marrow derived osteoclast-like ceils is sensitive to fluid shear stress, which suggests osteoclast-like ceils modulate their function in response to fluid shear stress through the change of free Ca^2+ concentration.
关 键 词:破骨细胞 激光扫描共聚焦显微镜 流体切应力
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