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作 者:郭世梁[1] 张颖丽[2] 张影杰[3] 柏祥娥[2]
机构地区:[1]南京大学医学院附属口腔医院牙体牙髓科江苏南京210008 [2]吉林大学口腔医学院牙体牙髓科 [3]吉林大学中日联谊医院手术室
出 处:《口腔医学研究》2011年第12期1029-1031,1035,共4页Journal of Oral Science Research
基 金:吉林省科技发展计划(编号:200905178)
摘 要:目的:观察rhIL-1β对培养的HDPCs产生蛋白质的影响,揭示rhIL-1β与牙髓炎的关系。方法:在HD-PCs的培养液中加入rhIL-1β,用2-DE分离HDPCs全蛋白,获得对照组和诱导组HDPCs蛋白质图谱,ImageMaster2DElit 5.0软件分析确认差异表达蛋白。结果:比较对照组和诱导组蛋白质图谱,发现了39个蛋白质点差异明显。其中15个蛋白质点在诱导组高表达,新增13个蛋白质点,7个蛋白质点低表达,4个蛋白质点仅在对照组中表达。结论:HDPCs对rhIL-1β的应答反应是一个非常复杂的过程,多种蛋白质分子涉及其中。Objective: To study the effects of recombinant human interleukin-1β(rhIL-1β)on the production of protein by human dental pulp cells in vitro and reveal the possible relationship between IL-1β and pulpitis.Methods: HDPCs were induced with rhIL-1β and the dental pulp cells entire protein was separated by a 2-Delectrophoresis technique.The rhIL-1β induction and the normal dental pulp cells protein 2-Delectrophoresis atlas were established.Difference expression protein was confirmed by ImageMaster 2D Elite 5.0 software analysis.Results: Comparing the two groups of protein 2-Delectrophoresis atlas,39 protein spots were obviously different.15 points in the induction of protein expression were higher,13 protein spots were new 7 protein points expressions were lower,and 4 points only were in the control group.Conclusion: Pulp cells to rhIL-1β responsiveness is a very complex process,which involve a variety of protein molecules.
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